INDOLINE COMPOUNDS FOR INHIBITING KIF18A
20230147507 · 2023-05-11
Assignee
Inventors
Cpc classification
C07D409/12
CHEMISTRY; METALLURGY
C07D491/107
CHEMISTRY; METALLURGY
C07D491/113
CHEMISTRY; METALLURGY
C07D405/12
CHEMISTRY; METALLURGY
C07D403/06
CHEMISTRY; METALLURGY
C07D403/12
CHEMISTRY; METALLURGY
C07D405/06
CHEMISTRY; METALLURGY
C07F9/5728
CHEMISTRY; METALLURGY
C07D491/22
CHEMISTRY; METALLURGY
C07D401/06
CHEMISTRY; METALLURGY
C07D401/12
CHEMISTRY; METALLURGY
C07D403/10
CHEMISTRY; METALLURGY
C07D413/12
CHEMISTRY; METALLURGY
C07D409/06
CHEMISTRY; METALLURGY
International classification
A61P35/00
HUMAN NECESSITIES
C07D401/12
CHEMISTRY; METALLURGY
C07D403/12
CHEMISTRY; METALLURGY
C07D401/06
CHEMISTRY; METALLURGY
C07D405/06
CHEMISTRY; METALLURGY
C07D405/12
CHEMISTRY; METALLURGY
C07D403/06
CHEMISTRY; METALLURGY
C07D409/06
CHEMISTRY; METALLURGY
C07D491/113
CHEMISTRY; METALLURGY
C07D413/12
CHEMISTRY; METALLURGY
C07D409/12
CHEMISTRY; METALLURGY
C07D491/107
CHEMISTRY; METALLURGY
Abstract
The present disclosure relates generally to inhibitors of KIF18A, compositions thereof, and methods of using said compounds and compositions thereof. More specifically, the present disclosure relates to indoline inhibitors of KIF18A and methods of their use for treating disease mediated by KIF18A, such as cancer.
Claims
1. A compound of Formula (I): ##STR01320## or a pharmaceutically acceptable salt thereof, wherein: ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo; R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon; each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; m is 0, 1, 2, 3, or 4; Y.sup.1 is N or CR.sup.C1; Y.sup.2 is N or CR.sup.C2; Y.sup.3 is N or CR.sup.C3; Y.sup.4 is N or CR.sup.C4; wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N; R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH; R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
2. The compound of claim 1, which is a compound of Formula (I-2): ##STR01321## or a pharmaceutically acceptable salt thereof, wherein: ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo; R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon; each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; m is 0, 1, 2, 3, or 4; Y.sup.1 is N or CR.sup.C1; Y.sup.2 is N or CR.sup.C2; Y.sup.3 is N or CR.sup.C3; Y.sup.4 is N or CR.sup.C4; wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N; R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH; R.sup.c1-R.sup.c15 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
3. The compound of claim 1, which is a compound of Formula (I-1): ##STR01322## or a pharmaceutically acceptable salt thereof, wherein: ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, and —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20; R.sup.a1-R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon; each R.sup.B group is independently halo, C.sub.1-6 alkyl, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; m is 0, 1, 2, 3, or 4; Y.sup.1 is N or CR.sup.C1; Y.sup.2 is N or CR.sup.C2; Y.sup.3 is N or CR.sup.C3; Y.sup.4 is N or CR.sup.C4; wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N; R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —NS(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH; R.sup.c1-R.sup.c13 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
4. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein the compound is not 4′-fluoro-1′-[3-(piperidine-1-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; 3-cyclopropyl-1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; 1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]-3-(propan-2-yl)urea; [4-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]methanol; 4′-fluoro-1′-(1H-indole-5-carbonyl)-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; N-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]pyrimidin-2-amine; 4′-fluoro-1′-[3-(morpholine-4-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; [3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; or salt of any of the foregoing.
5. The compound of claim 1, which is a compound of Formula (I-3): ##STR01323## or a pharmaceutically acceptable salt thereof, wherein: ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo; R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon; m is 2; the two R.sup.B groups are attached to the same carbon atom on ring B and are taken together with the carbon atom to which they are attached to form C.sub.3-7 cycloalkyl; Y.sup.1 is N or CR.sup.C1; Y.sup.2 is N or CR.sup.C2; Y.sup.3 is N or CR.sup.C3; Y.sup.4 is N or CR.sup.C4; wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N; R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH; R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
6. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted C.sub.6-14 aryl.
7. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted phenyl.
8. The compound of claim 1, which is a compound of Formula (Ia1): ##STR01324## or a pharmaceutically acceptable salt thereof, wherein: R.sup.a14 and R.sup.a15 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon; each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; m is 0, 1, 2, 3, or 4; R.sup.C2 is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH; R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
9. The compound of claim 8, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH; and R.sup.c1-R.sup.c13 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
10. The compound of claim 8, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is —NR.sup.c5S(O).sub.2R.sup.c6, and R.sup.c5 and R.sup.c6 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
11. The compound of claim 1, which is a compound of Formula (Ia2): ##STR01325## or a pharmaceutically acceptable salt thereof, wherein: R.sup.a16 is hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon; each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; m is 0, 1, 2, 3, or 4; R.sup.C2 is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15—NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH; R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
12-16. (canceled)
17. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R.sup.a14 and R.sup.a15 are each independently hydrogen; C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —OH, —O(C.sub.1-6 alkyl), —S(C.sub.1-6 alkyl), and halo; C.sub.2-6 alkenyl; C.sub.3-10 cycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, halo, cyano, —OH, —O(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of —OH, —O(C.sub.1-6 alkyl), and halo, wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; C.sub.3-10 cycloalkenyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one or more C.sub.1-6 alkyl.
18. The compound of claim 17, or a pharmaceutically acceptable salt thereof, wherein R.sup.a14 is hydrogen and R.sup.a15 is tert-butyl.
19. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein ring A is substituted with one or more substituents independently selected from the group consisting of fluoro, chloro, —OH, methyl, amino, ##STR01326## ##STR01327## ##STR01328## ##STR01329##
20. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein ring A is phenyl substituted with ##STR01330##
21-23. (canceled)
24. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein ##STR01331## of Formula (I) is ##STR01332## wherein * denotes the point of attachment to the rest of Formula (I).
25. (canceled)
26. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4, wherein R.sup.C1, R.sup.C3, and R.sup.C4 are each independently hydrogen, halo, or —NH.sub.2.
27-30. (canceled)
31. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is cyano, —OH, —CH.sub.2OH, bromo, —NO.sub.2, ##STR01333##
32. (canceled)
33. A compound of Formula (II): ##STR01334## or a pharmaceutically acceptable salt thereof, wherein: ring A is ##STR01335## wherein Z.sup.1, Z.sup.2, Z.sup.3, and Z.sup.4 are each independently hydrogen or R.sup.D, wherein R.sup.D is halo, —OH, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, —P(O)(R.sup.a23)(R.sup.a24), —C═NR.sup.a25, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo or C.sub.1-3 alkyl, provided that (1) when Z.sup.4 is hydrogen, then at least one of Z.sup.1 and Z.sup.3 is R.sup.D; and (2) when Z.sup.4 is R.sup.D, then Z.sup.1 is R.sup.D, or ##STR01336## wherein is a single bond or a double bond, Z.sup.5 is C—H, N, O, S, or N—X, wherein X is H or C.sub.1-6alkyl; Z.sup.6 is —NR.sup.a26C(O)NR.sup.a27R.sup.a2, —NR.sup.a29C(O)OR.sup.a30, —N═S(O)R.sup.a31R.sup.a32, —S(O)R.sup.a33, —S(O)(NR.sup.a34)R.sup.a35, —S(O).sub.2NR.sup.a36R.sup.a37, —S(O).sub.2R.sup.a38, —SR.sup.a39, 3- to 10-membered heterocycloalkyl, —C(O)R.sup.a40, or —CH(Z.sup.7)(Z.sup.8), wherein Z.sup.7 is hydrogen or —OH, and Z.sup.8 is C.sub.1-6 alkyl, C.sub.3-10 cycloalkyl optionally substituted with one or more halo, or 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo, and ring C is 5- to 6-membered heteroaryl optionally substituted with one or more R.sup.E substituents, wherein each R.sup.E substituent is independently selected from the group consisting of halo, —OH, and C.sub.1-6 alkyl, or two R.sup.E substituents are taken, together with the atoms to which they are attached, to form C.sub.5-6 cycloalkyl, C.sub.5-6 cycloalkenyl, 5- to 6-membered heterocycloalkyl, 5- to 6-membered heterocycloalkenyl, or 5- to 6-membered heteroaryl; R.sup.a4-R.sup.a40 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon; each R.sup.B group is independently halo or C.sub.1-6 alkyl optionally substituted with one or more halo; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together to form a ═CR.sup.1a3R.sup.1a4 group, wherein R.sup.1a3 and R.sup.1a4 are each independently hydrogen or C.sub.1-6 alkyl; m is 0, 1, 2, 3, or 4; Y.sup.1 is N or CR.sup.C1; Y.sup.2 is N or CR.sup.C2; Y.sup.3 is N or CR.sup.C3; Y.sup.4 is N or CR.sup.C4; wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N; R.sup.C1-R.sup.C4 are each independently hydrogen or R.sup.F, wherein R.sup.F is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, —O—S(O).sub.2R.sup.c19, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of halo and —OH, and R.sup.c1-R.sup.c19 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —O(C.sub.1-6 alkyl), —NHC(O)(C.sub.1-6 alkyl), and —OH; provided that (1) when ring B is unsubstituted cyclopentyl, then ring A is ##STR01337## wherein at least one of Z.sup.1-Z.sup.4 is —S(O).sub.2-(3- to 10-membered heterocycloalkyl) substituted with one or more halo, (2) when ring B is unsubstituted cyclohexyl and ring A is ##STR01338## then at least one of R.sup.C1-R.sup.C4 is R.sup.F, and (3) when ring B is 5- to 7-membered heterocycloalkyl optionally substituted with 1-4 R.sup.B, then ring A is ##STR01339## wherein at least one of Z.sup.1-Z.sup.4 is —S(O).sub.2-(3- to 10-membered heterocycloalkyl) optionally substituted with one or more halo.
34. The compound of claim 33, or a pharmaceutically acceptable salt thereof, wherein ring A is ##STR01340## wherein Z.sup.4 is hydrogen, and at least one of Z.sup.1 and Z.sup.3 is R.sup.D, wherein R.sup.D is halo, —OH, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, —P(O)(R.sup.a23)(R.sup.a24), —C═NR.sup.a25, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo or C.sub.1-3 alkyl.
35-36. (canceled)
37. The compound of claim 33, or a pharmaceutically acceptable salt thereof, wherein one or more of Z.sup.1-Z.sup.4 is selected from the group consisting of fluoro, chloro, —OH, —NH.sub.2, —CH.sub.2OH, ##STR01341## ##STR01342## ##STR01343## ##STR01344## ##STR01345##
38. The compound of claim 33, or a pharmaceutically acceptable salt thereof, wherein one of Z.sup.1-Z.sup.4 is ##STR01346##
39-50. (canceled)
51. The compound of claim 33, or a pharmaceutically acceptable salt thereof, wherein ##STR01347## of Formula (II) is ##STR01348## wherein * denotes the point of attachment to the rest of Formula (II).
52. The compound of claim 51, or a pharmaceutically acceptable salt thereof, wherein ##STR01349## of Formula (II) is ##STR01350##
53. The compound of claim 33, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4, wherein R.sup.C1, R.sup.C3, and R.sup.C4 are each independently hydrogen, halo, or —NH.sub.2.
54-60. (canceled)
61. The compound of claim 33, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is cyano, —OH, —CH.sub.2OH, fluoro, bromo, —NO.sub.2, ##STR01351##
62. The compound of claim 61, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is ##STR01352##
63. A compound, or a pharmaceutically acceptable salt thereof, selected from the group consisting of compounds of Table 1.
64. (canceled)
65. A pharmaceutical composition comprising a compound of claim 1, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
66. A method of inhibiting KIF18A comprising contacting a cell with an effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof.
67. A method of treating a disease or condition mediated by KIF18A in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof.
68. A method of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof.
69. The method of claim 68, wherein the cancer is selected from the group consisting of carcinomas, cancer of the anus, bladder, breast, colon, small intestine, appendix, kidney, renal pelvis, ureter, urothelium, liver, lung, pleura, esophagus, head and neck, nasopharynx, oropharynx, hypopharynx, oral cavity, larynx, biliary tract, gall-bladder, ovary, testicle, germ cell, uterus, pancreas, stomach, cervix, thyroid, prostate, salivary gland, or skin, hematopoietic tumors of lymphoid lineage, hematopoietic tumors of myeloid lineage, hematopoietic tumors of any lineage, myeloma, tumors of mesenchymal origin including sarcomas, tumors of the central and peripheral nervous system, tumor of neuroendocrine origin, tumor of endocrine origin, small cell tumors, tumors of unknown primary, other tumors comprising retinoblastoma, melanoma, seminoma, teratocarcinoma, osteosarcoma, and other cancer-related disorders that are a consequence of cancer presence or progression.
Description
DESCRIPTION OF FIGURES
[0009]
[0010]
[0011]
[0012]
[0013]
[0014]
DETAILED DESCRIPTION
[0015] The following description is presented to enable a person of ordinary skill in the art to make and use the various embodiments. Descriptions of specific devices, techniques, and applications are provided only as examples. Various modifications to the examples described herein will be readily apparent to those of ordinary skill in the art, and the general principles defined herein may be applied to other examples and applications without departing from the spirit and scope of the various embodiments. Thus, the various embodiments are not intended to be limited to the examples described herein and shown, but are to be accorded the scope consistent with the claims.
[0016] As used in the present specification, the following words and phrases are generally intended to have the meanings as set forth below, except to the extent that the context in which they are used indicates otherwise.
[0017] Throughout this application, unless the context indicates otherwise, references to a compound of Formula (I), Formula (I-1), Formula (Ia1), Formula (Ia2), Formula (I-2), Formula (I-3), Formula (Ia1), Formula (Ia2), or Formula (II) include all subgroups defined herein, such as Formula (I-1), (Ia1), or (Ia2), including all substructures, subgenera, preferences, embodiments, examples and particular compounds defined and/or described herein. In some embodiments, references to a compound of Formula (I), Formula (I-1), Formula (Ia1), Formula (Ia2), Formula (I-2), Formula (I-3), Formula (Ia1), Formula (Ia2), or Formula (II), and subgroups thereof, such as Formula (I-1), (Ia1), or (Ia2), include ionic forms, polymorphs, pseudopolymorphs, amorphous forms, solvates, co-crystals, chelates, isomers, tautomers, oxides (e.g., N-oxides, S-oxides), esters, prodrugs, isotopes and/or protected forms thereof. In some embodiments, references to a compound of Formula (I), Formula (I-1), Formula (Ia1), Formula (Ia2), Formula (I-2), Formula (I-3), Formula (Ia1), Formula (Ia2), or Formula (II), and subgroups thereof, such as Formula (I-1), (Ia1), or (Ia2), include polymorphs, solvates, co-crystals, isomers, tautomers and/or oxides thereof. In some embodiments, references to a compound of Formula (I), Formula (I-1), Formula (I-2), Formula (I-3), Formula (Ia1), Formula (Ia2), or Formula (II), and subgroups thereof, such as Formula (I-1), (Ia1), or (Ia2), include polymorphs, solvates, and/or co-crystals thereof. In some embodiments, references to a compound of Formula (I), Formula (I-1), Formula (I-2), Formula (I-3), Formula (Ia1), Formula (Ia2), or Formula (II), and subgroups thereof, such as Formula (I-1), (Ia1), or (Ia2), include isomers, tautomers and/or oxides thereof. In some embodiments, references to a compound of Formula (I), Formula (I-1), Formula (I-2), Formula (I-3), Formula (Ia1), Formula (Ia2), or Formula (II), and subgroups thereof, such as Formula (I-1), (Ia1), or (Ia2), include solvates thereof.
[0018] “Alkyl” encompasses straight and branched carbon chains having the indicated number of carbon atoms, for example, from 1 to 20 carbon atoms, or 1 to 8 carbon atoms, or 1 to 6 carbon atoms, or 1 to 3 carbon atoms. For example, C.sub.1-6 alkyl encompasses both straight and branched chain alkyl of from 1 to 6 carbon atoms. When an alkyl residue having a specific number of carbons is named, all branched and straight chain versions having that number of carbons are intended to be encompassed; thus, for example, “propyl” includes n-propyl and isopropyl; and “butyl” includes n-butyl, sec-butyl, isobutyl and t-butyl. Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, 2-pentyl, 3-pentyl, isopentyl, neopentyl, hexyl, 2-hexyl, 3-hexyl, and 3-methylpentyl.
[0019] When a range of values is given (e.g., C.sub.1-6 alkyl), each value within the range as well as all intervening ranges are included. For example, “C.sub.1-6 alkyl” includes C.sub.1, C.sub.2, C.sub.3, C.sub.4, C.sub.5, C.sub.6, C.sub.1-6, C.sub.2-6, C.sub.3-6, C.sub.4-6, C.sub.5-6, C.sub.1-5, C.sub.2-5, C.sub.3-5, C.sub.4-5, C.sub.1-4, C.sub.2-4, C.sub.3-4, C.sub.1-3, C.sub.2-3, and C.sub.1-2 alkyl.
[0020] “Alkenyl” refers to an unsaturated branched or straight-chain alkyl group having the indicated number of carbon atoms (e.g., 2 to 8, or 2 to 6 carbon atoms) and at least one carbon-carbon double bond. The group may be in either the cis or trans configuration (Z or E configuration) about the double bond(s). Alkenyl groups include, but are not limited to, ethenyl, propenyl (e.g., prop-1-en-1-yl, prop-1-en-2-yl, prop-2-en-1-yl (allyl), prop-2-en-2-yl), and butenyl (e.g., but-1-en-1-yl, but-1-en-2-yl, 2-methyl-prop-1-en-1-yl, but-2-en-1-yl, but-2-en-1-yl, but-2-en-2-yl, buta-1,3-dien-1-yl, buta-1,3-dien-2-yl).
[0021] “Alkynyl” refers to an unsaturated branched or straight-chain alkyl group having the indicated number of carbon atoms (e.g., 2 to 8 or 2 to 6 carbon atoms) and at least one carbon-carbon triple bond. Alkynyl groups include, but are not limited to, ethynyl, propynyl (e.g., prop-1-yn-1-yl, prop-2-yn-1-yl) and butynyl (e.g., but-1-yn-1-yl, but-1-yn-3-yl, but-3-yn-1-yl).
[0022] “Cycloalkyl” indicates a non-aromatic, fully saturated carbocyclic ring having the indicated number of carbon atoms, for example, 3 to 10, or 3 to 8, or 3 to 6 ring carbon atoms. Cycloalkyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl, as well as bridged and caged ring groups (e.g., norbornane, bicyclo[2.2.2]octane). In addition, one ring of a polycyclic cycloalkyl group may be aromatic, provided the polycyclic cycloalkyl group is bound to the parent structure via a non-aromatic carbon. For example, a 1,2,3,4-tetrahydronaphthalen-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is a cycloalkyl group, while 1,2,3,4-tetrahydronaphthalen-5-yl (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a cycloalkyl group. Examples of polycyclic cycloalkyl groups consisting of a cycloalkyl group fused to an aromatic ring are described below.
[0023] “Cycloalkenyl” indicates a non-aromatic carbocyclic ring, containing the indicated number of carbon atoms (e.g., 3 to 10, or 3 to 8, or 3 to 6 ring carbon atoms) and at least one carbon-carbon double bond. Cycloalkenyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of cycloalkenyl groups include cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclopentadienyl, and cyclohexenyl, as well as bridged and caged ring groups (e.g., bicyclo[2.2.2]octene). In addition, one ring of a polycyclic cycloalkenyl group may be aromatic, provided the polycyclic alkenyl group is bound to the parent structure via a non-aromatic carbon atom. For example, inden-1-yl (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is considered a cycloalkenyl group, while inden-4-yl (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a cycloalkenyl group. Examples of polycyclic cycloalkenyl groups consisting of a cycloalkenyl group fused to an aromatic ring are described below.
[0024] “Aryl” indicates an aromatic carbocyclic ring having the indicated number of carbon atoms, for example, 6 to 12 or 6 to 10 carbon atoms. Aryl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). In some instances, both rings of a polycyclic aryl group are aromatic (e.g., naphthyl). In other instances, polycyclic aryl groups may include a non-aromatic ring fused to an aromatic ring, provided the polycyclic aryl group is bound to the parent structure via an atom in the aromatic ring. Thus, a 1,2,3,4-tetrahydronaphthalen-5-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is considered an aryl group, while 1,2,3,4-tetrahydronaphthalen-1-yl (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is not considered an aryl group. Similarly, a 1,2,3,4-tetrahydroquinolin-8-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is considered an aryl group, while 1,2,3,4-tetrahydroquinolin-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic nitrogen atom) is not considered an aryl group. However, the term “aryl” does not encompass or overlap with “heteroaryl,” as defined herein, regardless of the point of attachment (e.g., both quinolin-5-yl and quinolin-2-yl are heteroaryl groups). In some instances, aryl is phenyl or naphthyl. In certain instances, aryl is phenyl. Additional examples of aryl groups comprising an aromatic carbon ring fused to a non-aromatic ring are described below.
[0025] “Heteroaryl” indicates an aromatic ring containing the indicated number of atoms (e.g., 5 to 12, or 5 to 10 membered heteroaryl) made up of one or more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms) selected from N, O and S and with the remaining ring atoms being carbon. Heteroaryl groups do not contain adjacent S and O atoms. In some embodiments, the total number of S and O atoms in the heteroaryl group is not more than 2. In some embodiments, the total number of S and O atoms in the heteroaryl group is not more than 1. Unless otherwise indicated, heteroaryl groups may be bound to the parent structure by a carbon or nitrogen atom, as valency permits. For example, “pyridyl” includes 2-pyridyl, 3-pyridyl and 4-pyridyl groups, and “pyrrolyl” includes 1-pyrrolyl, 2-pyrrolyl and 3-pyrrolyl groups.
[0026] In some instances, a heteroaryl group is monocyclic. Examples include pyrrole, pyrazole, imidazole, triazole (e.g., 1,2,3-triazole, 1,2,4-triazole, 1,2,4-triazole), tetrazole, furan, isoxazole, oxazole, oxadiazole (e.g., 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole), thiophene, isothiazole, thiazole, thiadiazole (e.g., 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,3,4-thiadiazole), pyridine, pyridazine, pyrimidine, pyrazine, triazine (e.g., 1,2,4-triazine, 1,3,5-triazine) and tetrazine.
[0027] In some instances, both rings of a polycyclic heteroaryl group are aromatic. Examples include indole, isoindole, indazole, benzoimidazole, benzotriazole, benzofuran, benzoxazole, benzoisoxazole, benzoxadiazole, benzothiophene, benzothiazole, benzoisothiazole, benzothiadiazole, 1H-pyrrolo[2,3-b]pyridine, 1H-pyrazolo[3,4-b]pyridine, 3H-imidazo[4,5-b]pyridine, 3H-[1,2,3]triazolo[4,5-b]pyridine, 1H-pyrrolo[3,2-b]pyridine, 1H-pyrazolo[4,3-b]pyridine, 1H-imidazo[4,5-b]pyridine, 1H-[1,2,3]triazolo[4,5-b]pyridine, 1H-pyrrolo[2,3-c]pyridine, 1H-pyrazolo[3,4-c]pyridine, 3H-imidazo[4,5-c]pyridine, 3H-[1,2,3]triazolo[4,5-c]pyridine, 1H-pyrrolo[3,2-c]pyridine, 1H-pyrazolo[4,3-c]pyridine, 1H-imidazo[4,5-c]pyridine, 1H-[1,2,3]triazolo[4,5-c]pyridine, furo[2,3-b]pyridine, oxazolo[5,4-b]pyridine, isoxazolo[5,4-b]pyridine, [1,2,3]oxadiazolo[5,4-b]pyridine, furo[3,2-b]pyridine, oxazolo[4,5-b]pyridine, isoxazolo[4,5-b]pyridine, [1,2,3]oxadiazolo[4,5-b]pyridine, furo[2,3-c]pyridine, oxazolo[5,4-c]pyridine, isoxazolo[5,4-c]pyridine, [1,2,3]oxadiazolo[5,4-c]pyridine, furo[3,2-c]pyridine, oxazolo[4,5-c]pyridine, isoxazolo[4,5-c]pyridine, [1,2,3]oxadiazolo[4,5-c]pyridine, thieno[2,3-b]pyridine, thiazolo[5,4-b]pyridine, isothiazolo[5,4-b]pyridine, [1,2,3]thiadiazolo[5,4-b]pyridine, thieno[3,2-b]pyridine, thiazolo[4,5-b]pyridine, isothiazolo[4,5-b]pyridine, [1,2,3]thiadiazolo[4,5-b]pyridine, thieno[2,3-c]pyridine, thiazolo[5,4-c]pyridine, isothiazolo[5,4-c]pyridine, [1,2,3]thiadiazolo[5,4-c]pyridine, thieno[3,2-c]pyridine, thiazolo[4,5-c]pyridine, isothiazolo[4,5-c]pyridine, [1,2,3]thiadiazolo[4,5-c]pyridine, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, phthalazine, naphthyridine (e.g., 1,8-naphthyridine, 1,7-naphthyridine, 1,6-naphthyridine, 1,5-naphthyridine, 2,7-naphthyridine, 2,6-naphthyridine), imidazo[1,2-a]pyridine, 1H-pyrazolo[3,4-d]thiazole, 1H-pyrazolo[4,3-d]thiazole and imidazo[2,1-b]thiazole.
[0028] In other instances, polycyclic heteroaryl groups may include a non-aromatic ring (e.g., cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl) fused to a heteroaryl ring, provided the polycyclic heteroaryl group is bound to the parent structure via an atom in the aromatic ring. For example, a 4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is considered a heteroaryl group, while 4,5,6,7-tetrahydrobenzo[d]thiazol-5-yl (wherein the moiety is bound to the parent structure via a non-aromatic carbon atom) is not considered a heteroaryl group. Examples of polycyclic heteroaryl groups consisting of a heteroaryl ring fused to a non-aromatic ring are described below.
[0029] “Heterocycloalkyl” indicates a non-aromatic, fully saturated ring having the indicated number of atoms (e.g., 3 to 10, or 3 to 7, membered heterocycloalkyl) made up of one or more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms) selected from N, O and S and with the remaining ring atoms being carbon. Heterocycloalkyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of heterocycloalkyl groups include oxiranyl, aziridinyl, azetidinyl, pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl. Examples include thiomorpholine S-oxide and thiomorpholine S,S-dioxide. In addition, one ring of a polycyclic heterocycloalkyl group may be aromatic (e.g., aryl or heteroaryl), provided the polycyclic heterocycloalkyl group is bound to the parent structure via a non-aromatic carbon or nitrogen atom. For example, a 1,2,3,4-tetrahydroquinolin-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic nitrogen atom) is considered a heterocycloalkyl group, while 1,2,3,4-tetrahydroquinolin-8-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a heterocycloalkyl group. Examples of polycyclic heterocycloalkyl groups consisting of a heterocycloalkyl group fused to an aromatic ring are described below.
[0030] “Heterocycloalkenyl” indicates a non-aromatic ring having the indicated number of atoms (e.g., 3 to 10, or 3 to 7, membered heterocycloalkyl) made up of one or more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms) selected from N, O and S and with the remaining ring atoms being carbon, and at least one double bond derived by the removal of one molecule of hydrogen from adjacent carbon atoms, adjacent nitrogen atoms, or adjacent carbon and nitrogen atoms of the corresponding heterocycloalkyl. Heterocycloalkenyl groups may be monocyclic or polycyclic (e.g., bicyclic, tricyclic). Examples of heterocycloalkenyl groups include dihydrofuranyl (e.g., 2,3-dihydrofuranyl, 2,5-dihydrofuranyl), dihydrothiophenyl (e.g., 2,3-dihydrothiophenyl, 2,5-dihydrothiophenyl), dihydropyrrolyl (e.g., 2,3-dihydro-1H-pyrrolyl, 2,5-dihydro-1H-pyrrolyl), dihydroimidazolyl (e.g., 2,3-dihydro-1H-imidazolyl, 4,5-dihydro-1H-imidazolyl), pyranyl, dihydropyranyl (e.g., 3,4-dihydro-2H-pyranyl, 3,6-dihydro-2H-pyranyl), tetrahydropyridinyl (e.g., 1,2,3,4-tetrahydropyridinyl, 1,2,3,6-tetrahydropyridinyl) and dihydropyridine (e.g., 1,2-dihydropyridine, 1,4-dihydropyridine). In addition, one ring of a polycyclic heterocycloalkenyl group may be aromatic (e.g., aryl or heteroaryl), provided the polycyclic heterocycloalkenyl group is bound to the parent structure via a non-aromatic carbon or nitrogen atom. For example, a 1,2-dihydroquinolin-1-yl group (wherein the moiety is bound to the parent structure via a non-aromatic nitrogen atom) is considered a heterocycloalkenyl group, while 1,2-dihydroquinolin-8-yl group (wherein the moiety is bound to the parent structure via an aromatic carbon atom) is not considered a heterocycloalkenyl group. Examples of polycyclic heterocycloalkenyl groups consisting of a heterocycloalkenyl group fused to an aromatic ring are described below.
[0031] Examples of polycyclic rings consisting of an aromatic ring (e.g., aryl or heteroaryl) fused to a non-aromatic ring (e.g., cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl) include indenyl, 2,3-dihydro-1H-indenyl, 1,2,3,4-tetrahydronaphthalenyl, benzo[1,3]dioxolyl, tetrahydroquinolinyl, 2,3-dihydrobenzo[1,4]dioxinyl, indolinyl, isoindolinyl, 2,3-dihydro-1H-indazolyl, 2,3-dihydro-1H-benzo[d]imidazolyl, 2,3-dihydrobenzofuranyl, 1,3-dihydroisobenzofuranyl, 1,3-dihydrobenzo[c]isoxazolyl, 2,3-dihydrobenzo[d]isoxazolyl, 2,3-dihydrobenzo[d]oxazolyl, 2,3-dihydrobenzo[b]thiophenyl, 1,3-dihydrobenzo[c]thiophenyl, 1,3-dihydrobenzo[c]isothiazolyl, 2,3-dihydrobenzo[d]isothiazolyl, 2,3-dihydrobenzo[d]thiazolyl, 5,6-dihydro-4H-cyclopenta[d]thiazolyl, 4,5,6,7-tetrahydrobenzo[d]thiazolyl, 5,6-dihydro-4H-pyrrolo[3,4-d]thiazolyl, 4,5,6,7-tetrahydrothiazolo[5,4-c]pyridinyl, indolin-2-one, indolin-3-one, isoindolin-1-one, 1,2-dihydroindazol-3-one, 1H-benzo[d]imidazol-2(3H)-one, benzofuran-2(3H)-one, benzofuran-3(2H)-one, isobenzofuran-1(3H)-one, benzo[c]isoxazol-3(1H)-one, benzo[d]isoxazol-3(2H)-one, benzo[d]oxazol-2(3H)-one, benzo[b]thiophen-2(3H)-one, benzo[b]thiophen-3(2H)-one, benzo[c]thiophen-1(3H)-one, benzo[c]isothiazol-3(1H)-one, benzo[d]isothiazol-3(2H)-one, benzo[d]thiazol-2(3H)-one, 4,5-dihydropyrrolo[3,4-d]thiazol-6-one, 1,2-dihydropyrazolo[3,4-d]thiazol-3-one, quinolin-4(3H)-one, quinazolin-4(3H)-one, quinazoline-2,4(1H,3H)-dione, quinoxalin-2(1H)-one, quinoxaline-2,3(1H,4H)-dione, cinnolin-4(3H)-one, pyridin-2(1H)-one, pyrimidin-2(1H)-one, pyrimidin-4(3H)-one, pyridazin-3(2H)-one, 1H-pyrrolo[3,2-b]pyridin-2(3H)-one, 1H-pyrrolo[3,2-c]pyridin-2(3H)-one, 1H-pyrrolo[2,3-c]pyridin-2(3H)-one, 1H-pyrrolo[2,3-b]pyridin-2(3H)-one, 1,2-dihydropyrazolo[3,4-d]thiazol-3-one and 4,5-dihydropyrrolo[3,4-d]thiazol-6-one. As discussed herein, whether each ring is considered an aryl, heteroaryl, cycloalkyl, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl group is determined by the atom through which the moiety is bound to the parent structure.
[0032] “Halogen” or “halo” refers to fluoro, chloro, bromo or iodo.
[0033] “Haloalkyl” refers to alkyl substituted with one or more halogen. A haloalkyl group may have a halogen substituent at any valence-permitted location on the alkyl and may have any number of halogen substituents ranging from one to the maximum valence-permitted number. Particular haloalkyl groups have 1, 2, or 3 halogen substituents. Examples of haloalkyl groups include, but are not limited to, —CH.sub.2F, —CHF.sub.2, —CF.sub.3, —CH.sub.2CH.sub.2F, —CH.sub.2CHF.sub.2, —CH.sub.2CF.sub.3, —CH.sub.2Cl, —CHCl.sub.2, —CCl.sub.3, —CH.sub.2CH.sub.2C.sub.1, —CH.sub.2CHCl.sub.2, —CH.sub.2CCl.sub.3.
[0034] Unless otherwise indicated, compounds disclosed and/or described herein include all possible enantiomers, diastereomers, meso isomers and other stereoisomeric forms, including racemic mixtures, optically pure forms and intermediate mixtures thereof. Enantiomers, diastereomers, meso isomers and other stereoisomeric forms can be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques. Unless specified otherwise, when the compounds disclosed and/or described herein contain olefinic double bonds or other centers of geometric asymmetry, it is intended that the compounds include both E and Z isomers. When the compounds described herein contain moieties capable of tautomerization, and unless specified otherwise, it is intended that the compounds include all possible tautomers.
[0035] “Protecting group” has the meaning conventionally associated with it in organic synthesis, i.e., a group that selectively blocks one or more reactive sites in a multifunctional compound such that a chemical reaction can be carried out selectively on another unprotected reactive site, and such that the group can readily be removed after the selective reaction is complete. A variety of protecting groups are disclosed, for example, in T. H. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, Third Edition, John Wiley & Sons, New York (1999). For example, a “hydroxy protected form” contains at least one hydroxy group protected with a hydroxy protecting group. Likewise, amines and other reactive groups may similarly be protected.
[0036] The term “pharmaceutically acceptable salt” refers to a salt of any of the compounds herein which are known to be non-toxic and are commonly used in the pharmaceutical literature. In some embodiments, the pharmaceutically acceptable salt of a compound retains the biological effectiveness of the compounds described herein and are not biologically or otherwise undesirable. Examples of pharmaceutically acceptable salts can be found in Berge et al., Pharmaceutical Salts, J. Pharmaceutical Sciences, January 1977, 66(1), 1-19. Pharmaceutically acceptable acid addition salts can be formed with inorganic acids and organic acids. Inorganic acids from which salts can be derived include, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, and phosphoric acid. Organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, pyruvic acid, lactic acid, oxalic acid, malic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 2-hydroxyethylsulfonic acid, p-toluenesulfonic acid, stearic acid and salicylic acid. Pharmaceutically acceptable base addition salts can be formed with inorganic and organic bases. Inorganic bases from which salts can be derived include, for example, sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, and aluminum. Organic bases from which salts can be derived include, for example, primary, secondary, and tertiary amines; substituted amines including naturally occurring substituted amines; cyclic amines; and basic ion exchange resins. Examples of organic bases include isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, and ethanolamine. In some embodiments, the pharmaceutically acceptable base addition salt is selected from ammonium, potassium, sodium, calcium, and magnesium salts.
[0037] If the compound described herein is obtained as an acid addition salt, the free base can be obtained by basifying a solution of the acid salt. Conversely, if the compound is a free base, an addition salt, particularly a pharmaceutically acceptable addition salt, may be produced by dissolving the free base in a suitable organic solvent and treating the solution with an acid, in accordance with conventional procedures for preparing acid addition salts from base compounds (see, e.g., Berge et al., Pharmaceutical Salts, J. Pharmaceutical Sciences, January 1977, 66(1), 1-19). Those skilled in the art will recognize various synthetic methodologies that may be used to prepare pharmaceutically acceptable addition salts.
[0038] A “solvate” is formed by the interaction of a solvent and a compound. Suitable solvents include, for example, water and alcohols (e.g., ethanol). Solvates include hydrates having any ratio of compound to water, such as monohydrates, dihydrates and hemi-hydrates.
[0039] The term “substituted” means that the specified group or moiety bears one or more substituents including, but not limited to, substituents such as alkoxy, acyl, acyloxy, alkoxycarbonyl, carbonylalkoxy, acylamino, amino, aminoacyl, aminocarbonylamino, aminocarbonyloxy, cycloalkyl, cycloalkenyl, aryl, heteroaryl, aryloxy, cyano, azido, halo, hydroxyl, nitro, carboxyl, thiol, thioalkyl, alkyl, alkenyl, alkynyl, heterocycloalkyl, heterocycloalkenyl, aralkyl, aminosulfonyl, sulfonylamino, sulfonyl, oxo and the like. The term “unsubstituted” means that the specified group bears no substituents. Where the term “substituted” is used to describe a structural system, the substitution is meant to occur at any valency-allowed position on the system. When a group or moiety bears more than one substituent, it is understood that the substituents may be the same or different from one another. In some embodiments, a substituted group or moiety bears from one to five substituents. In some embodiments, a substituted group or moiety bears one substituent. In some embodiments, a substituted group or moiety bears two substituents. In some embodiments, a substituted group or moiety bears three substituents. In some embodiments, a substituted group or moiety bears four substituents. In some embodiments, a substituted group or moiety bears five substituents.
[0040] By “optional” or “optionally” is meant that the subsequently described event or circumstance may or may not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not. For example, “optionally substituted alkyl” encompasses both “alkyl” and “substituted alkyl” as defined herein. It will be understood by those skilled in the art, with respect to any group containing one or more substituents, that such groups are not intended to introduce any substitution or substitution patterns that are sterically impractical, synthetically non-feasible, and/or inherently unstable. It will also be understood that where a group or moiety is optionally substituted, the disclosure includes both embodiments in which the group or moiety is substituted and embodiments in which the group or moiety is unsubstituted.
[0041] The compounds disclosed and/or described herein can be enriched isotopic forms, e.g., enriched in the content of .sup.2H, .sup.3H, .sup.11C, .sup.13C and/or .sup.14C. In one embodiment, the compound contains at least one deuterium atom. Such deuterated forms can be made, for example, by the procedure described in U.S. Pat. Nos. 5,846,514 and 6,334,997. Such deuterated compounds may improve the efficacy and increase the duration of action of compounds disclosed and/or described herein. Deuterium substituted compounds can be synthesized using various methods, such as those described in: Dean, D., Recent Advances in the Synthesis and Applications of Radiolabeled Compounds for Drug Discovery and Development, Curr. Pharm. Des., 2000; 6(10); Kabalka, G. et al., The Synthesis of Radiolabeled Compounds via Organometallic Intermediates, Tetrahedron, 1989, 45(21), 6601-21; and Evans, E., Synthesis of radiolabeled compounds, J. Radioanal. Chem., 1981, 64(1-2), 9-32.
[0042] The term “pharmaceutically acceptable carrier” or “pharmaceutically acceptable excipient” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in pharmaceutical compositions is contemplated. Supplementary active ingredients can also be incorporated into the pharmaceutical compositions.
[0043] The terms “patient,” “individual,” and “subject” refer to an animal, such as a mammal, bird, or fish. In some embodiments, the patient or subject is a mammal. Mammals include, for example, mice, rats, dogs, cats, pigs, sheep, horses, cows and humans. In some embodiments, the patient, individual, or subject is a human, for example a human that has been or will be the object of treatment, observation or experiment. The compounds, compositions and methods described herein can be useful in both human therapy and veterinary applications.
[0044] The term “therapeutically effective amount” or “effective amount” refers to that amount of a compound disclosed and/or described herein that is sufficient to affect treatment, as defined herein, when administered to a patient in need of such treatment. A therapeutically effective amount of a compound may be an amount sufficient to treat a disease responsive to modulation (e.g., inhibition) of KIF18a. The therapeutically effective amount will vary depending upon, for example, the subject and disease condition being treated, the weight and age of the subject, the severity of the disease condition, the particular compound, the dosing regimen to be followed, timing of administration, the manner of administration, all of which can readily be determined by one of ordinary skill in the art. The therapeutically effective amount may be ascertained experimentally, for example by assaying blood concentration of the chemical entity, or theoretically, by calculating bioavailability.
[0045] “Treatment” (and related terms, such as “treat,” “treated,” “treating”) includes one or more of: inhibiting a disease or disorder; slowing or arresting the development of clinical symptoms of a disease or disorder; and/or relieving a disease or disorder (i.e., causing relief from or regression of clinical symptoms). The term covers both complete and partial reduction of the condition or disorder, and complete or partial reduction of clinical symptoms of a disease or disorder. Thus, compounds described and/or disclosed herein may prevent an existing disease or disorder from worsening, assist in the management of the disease or disorder, or reduce or eliminate the disease or disorder.
[0046] It is understood that embodiments described herein as “comprising” include “consisting of” and “consisting essentially of” embodiments.
Compounds
[0047] Compounds and salts thereof (such as pharmaceutically acceptable salts) are detailed herein, including in the Brief Summary and in the appended claims. Also provided are the use of all of the compounds described herein, including any and all stereoisomers, including geometric isomers (cis/trans), E/Z isomers, enantiomers, diastereomers, and mixtures thereof in any ratio including racemic mixtures, salts and solvates of the compounds described herein, as well as methods of making such compounds. Any compound described herein may also be referred to as a drug.
[0048] In one aspect, provided are compounds of Formula (I):
##STR00008##
or a pharmaceutically acceptable salt thereof, wherein:
[0049] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo;
[0050] R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0051] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0052] each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0053] m is 0, 1, 2, 3, or 4;
[0054] Y.sup.1 is N or CR.sup.C1;
[0055] Y.sup.2 is N or CR.sup.C2;
[0056] Y.sup.3 is N or CR.sup.C3;
[0057] Y.sup.4 is N or CR.sup.C4;
[0058] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0059] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0060] R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0061] In one aspect, provided are compounds of Formula (I-1):
##STR00009##
or a pharmaceutically acceptable salt thereof, wherein:
[0062] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, and —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20.
[0063] R.sup.a1-R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0064] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0065] each R.sup.B group is independently halo, C.sub.1-6 alkyl, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0066] m is 0, 1, 2, 3, or 4;
[0067] Y.sup.1 is N or CR.sup.C1;
[0068] Y.sup.2 is N or CR.sup.C2;
[0069] Y.sup.3 is N or CR.sup.C3;
[0070] Y.sup.4 is N or CR.sup.C4;
[0071] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0072] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0073] R.sup.c1-R.sup.c13 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0074] In another aspect, provided herein is a compound of Formula (I-2)
##STR00010##
or a pharmaceutically acceptable salt thereof, wherein:
[0075] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo;
[0076] R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0077] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0078] each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0079] m is 0, 1, 2, 3, or 4;
[0080] Y.sup.1 is N or CR.sup.C1;
[0081] Y.sup.2 is N or CR.sup.C2;
[0082] Y.sup.3 is N or CR.sup.C3;
[0083] Y.sup.4 is N or CR.sup.C4;
[0084] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0085] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0086] R.sup.c1-R.sup.c15 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0087] In another aspect, provided herein is a compound of Formula (I-3):
##STR00011##
or a pharmaceutically acceptable salt thereof, wherein:
[0088] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo;
[0089] R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0090] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0091] m is 2;
[0092] the two R.sup.B groups are attached to the same carbon atom on ring B and are taken together with the carbon atom to which they are attached to form C.sub.3-7 cycloalkyl;
[0093] Y.sup.1 is N or CR.sup.C1;
[0094] Y.sup.2 is N or CR.sup.C2;
[0095] Y.sup.3 is N or CR.sup.C3;
[0096] Y.sup.4 is N or CR.sup.C4;
[0097] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0098] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0099] R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0100] In some embodiments of Formula (I), Formula (I-1), Formula (I-2), and Formula (I-3), or a pharmaceutically acceptable salt thereof, ring A is substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more halo. In some embodiments, ring A is substituted with —SR.sup.a21, —C(O)R.sup.a22, or C.sub.1-6 alkyl substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more halo. In some embodiments, R.sup.a21 and R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl.
[0101] In some embodiments of Formula (I), Formula (I-1), Formula (I-2), and Formula (I-3), or a pharmaceutically acceptable salt thereof, one or more R.sup.B groups are independently C.sub.1-6 alkyl substituted with one, two, three, four, five, or more halo. In some embodiments, an R.sup.B group is C.sub.1-6 alkyl substituted with one, two, three, four, five, or more halo.
[0102] In some embodiments of Formula (I), Formula (I-1), Formula (I-2), and Formula (I-3), or a pharmaceutically acceptable salt thereof, R.sup.C2 is —NR.sup.c14C(O)OR.sup.c15 wherein R.sup.c14 and R.sup.c15 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0103] In some embodiments, cycloalkyl or heterocycloalkyl groups include spiro groups. In some embodiments, cycloalkyl or heterocycloalkyl groups include fused groups.
[0104] In some embodiments of Formula (I), Formula (I-1), Formula (I-2), and Formula (I-3), or a pharmaceutically acceptable salt thereof, ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted. In some embodiments, ring A is optionally substituted C.sub.6-14 aryl. In some embodiments, ring A is optionally substituted phenyl. In some embodiments, ring A is optionally substituted 5- to 12-membered heteroaryl. In some embodiments, ring A is optionally substituted 6-membered heteroaryl. In some embodiments, ring A is optionally substituted 5-membered heteroaryl. In some embodiments, ring A is indolyl, indazolyl, pyridinyl, thiophenyl, furanyl, pyrazolyl, pyrrolyl, oxazolyl, chromanyl, or quinolinyl, each optionally substituted. In some embodiments, ring A is optionally substituted thiophenyl.
[0105] In some embodiments Formula (I), Formula (I-1), Formula (I-2), and Formula (I-3) Formula (II), ring A is optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo. In some embodiments, R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl.
[0106] In some embodiments, the 3- to 10-membered heterocycloalkyl is piperidinyl. In some embodiments, the 3- to 10-membered heterocycloalkyl is
##STR00012##
In some embodiments, R.sup.a1 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a1 is hydrogen. In some embodiments, R.sup.a2 and R.sup.a3 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a2 and R.sup.a3 are each independently hydrogen, cyclopropyl, ethyl, or isopropyl. In some embodiments, R.sup.a4 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a4 is hydrogen. In some embodiments, R.sup.a5 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a5 is tert-butyl. In some embodiments, R.sup.a6 and R.sup.ay are each independently hydrogen, C.sub.1-6 alkyl, or 5- to 12-membered heteroaryl optionally substituted with C.sub.1-6 alkyl. In some embodiments, R.sup.a6 and R.sup.ay are each independently hydrogen, imidazolyl, methylimidazolyl, or pyrimidinyl. In some embodiments, —N═S(O)R.sup.a8R.sup.a9 is
##STR00013##
In some embodiments, R.sup.a8 and R.sup.a9 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a8 and R.sup.a9 are each independently methyl or cyclopentyl. In some embodiments, —OR.sup.a10 is
##STR00014##
In some embodiments, R.sup.a10 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a10 is cyclopentyl. In some embodiments, —S(O)R.sup.a11 is
##STR00015##
In some embodiments, R.sup.a11 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a11 is cyclopentyl. In some embodiments, —S(O)(NR.sup.a12)R.sup.a13 is
##STR00016##
In some embodiments, R.sup.a12 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a12 is hydrogen or methyl. In some embodiments, R.sup.a13 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a13 is cyclopentyl. In some embodiments, —S(O).sub.2NR.sup.a14R.sup.a15 is
##STR00017## ##STR00018##
In some embodiments, —S(O).sub.2N.sup.a14R.sup.a15 is
##STR00019## ##STR00020##
In some embodiments, R.sup.a14 and R.sup.a15 are each independently hydrogen; C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —OH, —O(C.sub.1-6 alkyl), —S(C.sub.1-6 alkyl), and halo; C.sub.2-6 alkenyl; C.sub.3-10 cycloalkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, halo, cyano, —OH, —O(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, —O(C.sub.1-6 alkyl), and halo, wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; C.sub.3-10 cycloalkenyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more C.sub.1-6 alkyl. In some embodiments, R.sup.a14 and R.sup.a15 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a14 is hydrogen and R.sup.a15 is butyl. In some embodiments, R.sup.a15 is tert-butyl. In some embodiments, —S(O).sub.2R.sup.a15 is
##STR00021## ##STR00022##
In some embodiments, —S(O).sub.2R.sup.a16 is
##STR00023##
In some embodiments, R.sup.a16 is C.sub.3-10 cycloalkyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.1-6 alkyl or halo. In some embodiments, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20 is —C(O)NR.sup.a19R.sup.a20 or —(CR.sup.a17R.sup.a18)C(O)NR.sup.a19R.sup.a20. In some embodiments, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20 is —C(O)NR.sup.a19R.sup.a20. In some embodiments, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20 is —(CR.sup.a17R.sup.a18)C(O)NR.sup.a19R.sup.a20. In some embodiments, R.sup.a17 and R.sup.a18 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a17 and R.sup.a18 are each hydrogen. In some embodiments, R.sup.a19 and R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a19 and R.sup.a20 are each independently hydrogen or cyclopropyl. In some embodiments, —SR.sup.a21 is
##STR00024##
In some embodiments, R.sup.a21 is C.sub.3-10 cycloalkyl. In some embodiments, —C(O)R.sup.a22 is
##STR00025##
In some embodiments, R.sup.a22 is C.sub.3-10 cycloalkyl. In some embodiments, the optionally substituted C.sub.1-6 alkyl is
##STR00026##
In some embodiments, C.sub.1-6 alkyl is optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more halo. In some embodiments, the 3- to 10-membered heterocycloalkyl is piperidinyl optionally substituted with one, two, three, four, five, or more halo. In some embodiments, the 3- to 10-membered heterocycloalkyl is optionally substituted with one, two, three, four, five, or more fluoro. In some embodiments, the 3- to 10-membered heterocycloalkyl is piperidinyl optionally substituted with one, two, three, four, five, or more fluoro.
[0107] In some embodiments, ring A is substituted with one or more substituents independently selected from the group consisting of fluoro, chloro, —OH, amino,
##STR00027## ##STR00028## ##STR00029## ##STR00030##
In some embodiments, ring A is optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of fluoro, chloro, —OH amino,
##STR00031## ##STR00032## ##STR00033## ##STR00034##
[0108] In some embodiments of Formula (I), Formula (I-1), Formula (I-2), and Formula (I-3), or a pharmaceutically acceptable salt thereof, ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon. In some embodiments, ring B is C.sub.5-7 cycloalkyl. In some embodiments, ring B is cyclopentyl, cyclohexyl, or cycloheptyl. In some embodiments, ring B is
##STR00035##
wherein * denotes the point of attachment to the rest of Formula (I), Formula (I-1), Formula (I-2), or Formula (I-3). In some embodiments, ring B is C.sub.5-7 cycloalkenyl. In some embodiments, ring B is cyclopentenyl, cyclohexenyl, or cycloheptenyl. In some embodiments, ring B is
##STR00036##
wherein * denotes the point of attachment to the rest of Formula (I), Formula (I-1), Formula (I-2), or Formula (I-3). In some embodiments, ring B is
##STR00037##
wherein * denotes the point of attachment to the rest of Formula (I), Formula (I-1), Formula (I-2), or Formula (I-3). In some embodiments, ring B is 5- to 7-membered heterocycloalkyl. In some embodiments, ring B is 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon. In some embodiments, ring B is tetrahydrofuranyl or 1,3-dioxanyl. In some embodiments, ring B is
##STR00038##
wherein * denotes the point of attachment to the rest of Formula (I), Formula (I-1), Formula (I-2), or Formula (I-3).
[0109] In some embodiments, ring B is substituted with m R.sup.B groups, wherein each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl. In some embodiment, an R.sup.B group is methyl or ethyl. In some embodiment, two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form cyclopropyl. In some embodiments, two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form cyclopropyl.
[0110] In some embodiments, m is 0, 1, 2, 3, or 4. In some embodiments, m is 0, 1, 2, or 3. In some embodiments, m is 0, 1, or 2. In some embodiments, m is 0 or 1. In some embodiments, m is 0. In some embodiments, m is 1.
[0111] In some embodiments,
##STR00039##
of Formula (I), Formula (I-1), Formula (I-2), or Formula (I-3), is
[0112] ##STR00040##
wherein * denotes the point of attachment to the rest of Formula (I), Formula (I-1), Formula (I-2), or Formula (I-3). In some embodiments,
##STR00041##
of Formula I is
[0113] ##STR00042##
wherein * denotes the point of attachment to the rest of Formula (I), Formula (I-1), Formula (I-2), or Formula (I-3).
[0114] In some embodiments of Formula (I), Formula (I-1), Formula (I-2), and Formula (I-3), or a pharmaceutically acceptable salt thereof, Y.sup.1 is N or CR.sup.C1; Y.sup.2 is N or CR.sup.C2; Y.sup.3 is N or CR.sup.C3; and Y.sup.4 is N or CR.sup.C4. In some embodiments, no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N. In some embodiments, no more than two of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N. In some embodiments, no more than one of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 is N. In some embodiments, Y.sup.1 is CR.sup.C1; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4. In some embodiments, Y.sup.1 is N; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4 In some embodiments, Y.sup.1 is CR.sup.C1; Y.sup.2 is N; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
[0115] In some embodiments, R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH.
[0116] In some embodiments, R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.c1-R.sup.c15 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH.
[0117] In some embodiments, R.sup.C1 is hydrogen or halo. In some embodiments, R.sup.C1 is hydrogen or fluoro. In some embodiments, R.sup.C3 is hydrogen. In some embodiments, R.sup.C4 is hydrogen or —NH.sub.2. In some embodiments, R.sup.C1, R.sup.C3, and R.sup.C4 are each independently hydrogen, halo, or —NH.sub.2.
[0118] In some embodiments, R.sup.C2 is cyano, —OH, —CH.sub.2OH, bromo, —NO.sub.2,
##STR00043##
In some embodiments, R.sup.C2 is cyano, —OH, —CH.sub.2OH, bromo, —NO.sub.2,
##STR00044##
In some embodiments, R.sup.C2 is cyano, —OH, halo, —NO.sub.2, C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.C2 is cyano, —OH, halo, —NO.sub.2, C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH.
[0119] In some embodiments, —C(O)NR.sup.c1R.sup.c2 is
##STR00045##
In some embodiments, R.sup.c1 and R.sup.c2 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c1 and R.sup.c2 are each independently hydrogen, methyl, or ethyl. In some embodiments, —NR.sup.c3R.sup.c4 is
##STR00046##
In some embodiments, R.sup.c3 and R.sup.c4 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c1 and R.sup.c2 are each independently hydrogen, methyl, or ethyl. In some embodiments, —NR.sup.c5S(O).sub.2R.sup.c6 is
##STR00047##
In some embodiments, R.sup.c5 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c5 is hydrogen, methyl, or ethyl. In some embodiments, R.sup.c6 is hydrogen or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from halo and —OH. In some embodiments, R.sup.c5 is methyl or —CH.sub.2CH.sub.2OH. In some embodiments, R.sup.c5 is hydrogen. In some embodiments, R.sup.c6 is ethyl. In some embodiments, —P(O)R.sup.c7R.sup.c8 is
##STR00048##
In some embodiments, R.sup.c7 and R.sup.c8 are each independently C.sub.1-6 alkyl. In some embodiments, R.sup.c7 and R.sup.c8 are each methyl. In some embodiments, —N═S(O)R.sup.c9R.sup.c10 is
##STR00049##
In some embodiments, R.sup.c9 and R.sup.c10 are each independently C.sub.1-6 alkyl. In some embodiments, R.sup.c9 and R.sup.c10 are each methyl. In some embodiments, —S(O)(NR.sup.c11)R.sup.c12 is
##STR00050##
In some embodiments, R.sup.c11 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c11 is hydrogen or methyl. In some embodiments, R.sup.c12 is C.sub.1-6 alkyl or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.c12 is cyclopropyl. In some embodiments, —S(O).sub.2R.sup.c13 is
##STR00051##
In some embodiments, R.sup.c13 is C.sub.1-6 alkyl. In some embodiments, R.sup.c13 is methyl. In some embodiments, NR.sup.c14C(O)OR.sup.c15 is
##STR00052##
In some embodiments, R.sup.c14 and R.sup.c15 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c14 is hydrogen. In some embodiments, R.sup.c15 is ethyl. In some embodiments, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18 is
##STR00053##
In some embodiments, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18 is —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-3NR.sup.c17C(O)R.sup.c18. In some embodiments, R.sup.c16, R.sup.c17 and R.sup.c18 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c16 and R.sup.c17 are hydrogen. In some embodiments, R.sup.c18 is methyl.
[0120] In one aspect, provided are compounds of Formula (Ia1):
##STR00054##
or a pharmaceutically acceptable salt thereof, wherein R.sup.a14, R.sup.a15, ring B, R.sup.B, m, and R.sup.C2 are as defined for Formula (I) or any variation or embodiment thereof. In some embodiments, R.sup.C2 is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18 or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.C2 is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.C2 is —NR.sup.c5S(O).sub.2R.sup.c6. In some embodiments, R.sup.c5 is hydrogen and R.sup.C6 is C.sub.1-6 alkyl. In some embodiments, R.sup.c5 is hydrogen and R.sup.c6 is ethyl. In some embodiments, R.sup.c5 is hydrogen. In some embodiments, R.sup.c6 is ethyl. In some embodiments, R.sup.c6 is methyl. In some embodiments, R.sup.a14 is hydrogen and R.sup.a15 is C.sub.1-6 alkyl. In some embodiments, R.sup.a14 is hydrogen and R.sup.a15 is tert-butyl. In some embodiments, R.sup.a14 is hydrogen. In some embodiments, R.sup.a15 is tert-butyl. In some embodiments, ring B is
##STR00055##
wherein * denotes the point of attachment to the rest of Formula (Ia1). In some embodiments,
##STR00056##
of Formula (Ia1) is
[0121] ##STR00057##
[0122] In one aspect, provided are compounds of Formula (Ia2):
##STR00058##
or a pharmaceutically acceptable salt thereof, wherein R.sup.a16, ring B, R.sup.B, m, and R.sup.C2 are as defined for Formula (I) or any variation or embodiment thereof. In some embodiments, R.sup.C2 is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12—S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.C2 is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0123] In some embodiments, ring B is not
##STR00059##
wherein * denotes the point of attachment to the rest of Formula (I). In some embodiments, R.sup.C1 is not fluoro. In some embodiments, R.sup.C2 is not hydrogen. In some embodiments, ring B is not
##STR00060##
wherein * denotes the point of attachment to the rest of Formula (I); or R.sup.C1 is not fluoro; or R.sup.C2 is not hydrogen.
[0124] In some embodiments, the compound is not 4′-fluoro-1′-[3-(piperidine-1-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; 3-cyclopropyl-1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; 1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]-3-(propan-2-yl)urea; [4-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]methanol; 4′-fluoro-1′-(1H-indole-5-carbonyl)-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; N-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]pyrimidin-2-amine; 4′-fluoro-1′-[3-(morpholine-4-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; or [3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea.
[0125] In some embodiments, the compound is not a salt of 4′-fluoro-1′-[3-(piperidine-1-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; 3-cyclopropyl-1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; 1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]-3-(propan-2-yl)urea; [4-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]methanol; 4′-fluoro-1′-(1H-indole-5-carbonyl)-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; N-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]pyrimidin-2-amine; 4′-fluoro-1′-[3-(morpholine-4-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; or [3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea.
[0126] In another aspect, provided herein is a compound of Formula (II):
##STR00061##
or a pharmaceutically acceptable salt thereof, wherein:
[0127] ring A is
##STR00062##
wherein Z.sup.1, Z.sup.2, Z.sup.3, and Z.sup.4 are each independently hydrogen or R.sup.D, wherein R.sup.D is halo, —OH, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, —P(O)(R.sup.a23)(R.sup.a24), —C═NR.sup.a25, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo or C.sub.1-3 alkyl, [0128] provided that [0129] (1) when Z.sup.4 is hydrogen, then at least one of Z.sup.1 and Z.sup.3 is R.sup.D; and [0130] (2) when Z.sup.4 is R.sup.D, then Z.sup.1 is R.sup.D, or
##STR00063##
wherein [0131] is a single bond or a double bond, [0132] Z.sup.5 is C—H, N, O, S, or N—X, wherein X is H or C.sub.1-6alkyl. [0133] Z.sup.6 is —NR.sup.a26C(O)NR.sup.a27R.sup.a28, —NR.sup.a29C(O)OR.sup.a30, —N═S(O)R.sup.a31R.sup.a32, —S(O)R.sup.a33, —S(O)(NR.sup.a34)R.sup.a35, —S(O).sub.2NR.sup.a36R.sup.a37, —S(O).sub.2R.sup.a38, —SR.sup.a39, —C(O)R.sup.a40, 3- to 10-membered heterocycloalkyl, or —CH(Z.sup.7)(Z.sup.8), wherein Z.sup.7 is hydrogen or —OH, and Z.sup.8 is C.sub.1-6 alkyl, C.sub.3-10 cycloalkyl optionally substituted with one or more halo, or 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo, and [0134] ring C is 5- to 6-membered heteroaryl optionally substituted with one or more R.sup.E substituents, wherein each R.sup.E substituent is independently selected from the group consisting of halo, —OH, and C.sub.1-6 alkyl, or two R.sup.E substituents are taken, together with the atoms to which they are attached, to form C.sub.5-6 cycloalkyl, C.sub.5-6 cycloalkenyl, 5- to 6-membered heterocycloalkyl, 5- to 6-membered heterocycloalkenyl, or 5- to 6-membered heteroaryl;
[0135] R.sup.a4-R.sup.a40 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0136] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0137] each R.sup.B group is independently halo or C.sub.1-6 alkyl optionally substituted with one or more halo; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together to form a ═CR.sup.1a3R.sup.1a4 group, wherein R.sup.1a3 and R.sup.1a4 are each independently hydrogen or C.sub.1-6 alkyl;
[0138] m is 0, 1, 2, 3, or 4;
[0139] Y.sup.1 is N or CR.sup.C1;
[0140] Y.sup.2 is N or CR.sup.C2;
[0141] Y.sup.3 is N or CR.sup.C3;
[0142] Y.sup.4 is N or CR.sup.C4;
[0143] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0144] R.sup.C1-R.sup.c4 are each independently hydrogen or R.sup.F, wherein R.sup.F is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5 S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, —O—S(O).sub.2R.sup.c19, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of halo and —OH, and
[0145] R.sup.c1-R.sup.c19 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —O(C.sub.1-6 alkyl), —NHC(O)(C.sub.1-6 alkyl), and —OH;
[0146] provided that
[0147] (1) when ring B is unsubstituted cyclopentyl, then ring A is
##STR00064##
wherein at least one of Z.sup.1-Z.sup.4 is —S(O).sub.2-(3- to 10-membered heterocycloalkyl) substituted with one or more halo,
[0148] (2) when ring B is unsubstituted cyclohexyl and ring A is
##STR00065##
then at least one of R.sup.C1-R.sup.C4 is R.sup.F, and
[0149] (3) when ring B is 5- to 7-membered heterocycloalkyl optionally substituted with 1-4 R.sup.B, then ring A is
##STR00066##
wherein at least one of Z.sup.1-Z.sup.4 is —S(O).sub.2-(3- to 10-membered heterocycloalkyl) optionally substituted with one or more halo.
[0150] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, with one, two, three, or four Z.sup.1-Z.sup.4 are independently selected from the group consisting of —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more halo. In some embodiments, ring A is substituted with —SR.sup.a21, —C(O)R.sup.a22, or C.sub.1-6 alkyl substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more halo. In some embodiments, R.sup.a21 and R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl.
[0151] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, Z.sup.1, Z.sup.2, Z.sup.3, and Z.sup.4 are each independently hydrogen or R.sup.D, wherein R.sup.D is halo, —OH, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, —P(O)(R.sup.a23)(R.sup.a24), —C═NR.sup.a25, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo or C.sub.1-3 alkyl, wherein R.sup.a4-R.sup.a25 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl.
[0152] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, Z.sup.4 is hydrogen and at least one of Z.sup.1 and Z.sup.3 is R.sup.D wherein R.sup.D is as defined elsewhere herein. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, Z.sup.4 is when Z.sup.4 is R.sup.D and Z.sup.1 is R.sup.D wherein R.sup.D is as defined elsewhere herein.
[0153] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, Z.sup.5 is C—H, N, O, S, or N—X, wherein X is H or C.sub.1-6alkyl. In some embodiments, X is H. In some embodiments, X is C.sub.1-6alkyl. In some embodiments, X is methyl. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, Z.sup.5 is C—H, N, O, S, or N—X, wherein X is H or C.sub.1-6alkyl, Z.sup.6 is —NR.sup.a26C(O)NR.sup.a27R.sup.a28, —NR.sup.a29C(O)OR.sup.a30, —N═S(O)R.sup.a31R.sup.a32, —S(O)R.sup.a33, —S(O)(NR.sup.a34)R.sup.a35, —S(O).sub.2NR.sup.a36R.sup.a37, —S(O).sub.2R.sup.a38, —SR.sup.a39, 3- to 10-membered heterocycloalkyl, C(O)R.sup.a40, or —CH(Z.sup.7)(Z.sup.8), wherein Z.sup.7 is hydrogen or —OH, and Z.sup.8 is C.sub.1-6 alkyl, C.sub.3-10 cycloalkyl optionally substituted with one or more halo, or 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo, and ring C is 5- to 6-membered heteroaryl optionally substituted with one or more R.sup.E substituents, wherein each R.sup.E substituent is independently selected from the group consisting of halo, —OH, and C.sub.1-6 alkyl, or two R.sup.E substituents are taken, together with the atoms to which they are attached, to form C.sub.5-6 cycloalkyl, C.sub.5-6 cycloalkenyl, 5- to 6-membered heterocycloalkyl, 5- to 6-membered heterocycloalkenyl, or 5- to 6-membered heteroaryl; and R.sup.a26-R.sup.a40 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl.
[0154] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, one or more R.sup.B groups are independently C.sub.1-6 alkyl substituted with one, two, three, four, five, or more halo. In some embodiments, an R.sup.B group is C.sub.1-6 alkyl substituted with one, two, three, four, five, or more halo.
[0155] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, one or more R.sup.B groups are independently halo or C.sub.1-6 alkyl optionally substituted with one or more halo. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together to form a ═CR.sup.1a3R.sup.1a4 group, wherein R.sup.1a3 and R.sup.1a4 are each independently hydrogen or C.sub.1-6 alkyl.
[0156] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, R.sup.c2 is —NR.sup.c14C(O)OR.sup.c15 wherein R.sup.c14 and R.sup.c15 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0157] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, R.sup.C1-R.sup.C4 are each independently hydrogen or R.sup.F, wherein R.sup.F is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, —O—S(O).sub.2R.sup.c19, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of halo and —OH; and R.sup.c1-R.sup.c19 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —O(C.sub.1-6 alkyl), —NHC(O)(C.sub.1-6 alkyl), and —OH. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, R.sup.C1-R.sup.C4 are each independently hydrogen or R.sup.F, wherein R.sup.F is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13—NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of halo and —OH, and R.sup.c1-R.sup.c19 are as defined elsewhere herein. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, R.sup.C1-R.sup.C4 are each independently —O—S(O).sub.2R.sup.c19, wherein R.sup.c19 is as defined elsewhere herein.
[0158] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, ring B is unsubstituted cyclopentyl and at least one of Z.sup.1-Z.sup.4 is —S(O).sub.2-(3- to 10-membered heterocycloalkyl) is substituted with one or more halo. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, ring B is unsubstituted cyclohexyl, ring A is
##STR00067##
and at least one of R.sup.C1-R.sup.C4 is R.sup.F, wherein R.sup.C1-R.sup.C4 and R.sup.F are as defined elsewhere herein. In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, ring B is 5- to 7-membered heterocycloalkyl optionally substituted with 1-4 R.sup.B, and at least one of Z.sup.1-Z.sup.4 is —S(O).sub.2-(3- to 10-membered heterocycloalkyl) is optionally substituted with one or more halo, wherein R.sup.B is as defined elsewhere herein.
[0159] In some embodiments, cycloalkyl or heterocycloalkyl groups include spiro groups. In some embodiments, cycloalkyl or heterocycloalkyl groups include fused groups.
[0160] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted. In some embodiments, ring A is optionally substituted C.sub.6-14 aryl. In some embodiments, ring A is optionally substituted phenyl. In some embodiments, ring A is optionally substituted 5- to 12-membered heteroaryl. In some embodiments, ring A is optionally substituted 6-membered heteroaryl. In some embodiments, ring A is optionally substituted 5-membered heteroaryl. In some embodiments, ring A is indolyl, indazolyl, pyridinyl, thiophenyl, furanyl, pyrazolyl, pyrrolyl, oxazolyl, chromanyl, or quinolinyl, each optionally substituted. In some embodiments, ring A is optionally substituted thiophenyl.
[0161] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, ring A is optionally substituted phenyl. In some embodiments, ring A is optionally substituted 5- to 12-membered heteroaryl. In some embodiments, ring A is optionally substituted 6-membered heteroaryl. In some embodiments, ring A is optionally substituted 5-membered heteroaryl. In some embodiments, ring A is pyridinyl, thiophenyl, furanyl, pyrazolyl, pyrrolyl, or oxazolyl. In some embodiments, ring A is
##STR00068##
[0162] In some embodiments of Formula (II), R.sup.a4 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a4 is hydrogen. In some embodiments, R.sup.a5 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a5 is tert-butyl. In some embodiments, R.sup.a6 and R.sup.ay are each independently hydrogen, C.sub.1-6 alkyl, or 5- to 12-membered heteroaryl optionally substituted with C.sub.1-6 alkyl. In some embodiments, R.sup.a6 and R.sup.a7 are each independently hydrogen, imidazolyl, methylimidazolyl, or pyrimidinyl. In some embodiments, —N═S(O)R.sup.a8R.sup.a9 is
##STR00069##
In some embodiments, R.sup.a8 and R.sup.a9 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a8 and R.sup.a9 are each independently methyl or cyclopentyl. In some embodiments, —OR.sup.a10 is
##STR00070##
In some embodiments, R.sup.a10 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a10 is cyclopentyl. In some embodiments, —S(O)R.sup.a11 is
##STR00071##
In some embodiments, R.sup.a11 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a11 is cyclopentyl. In some embodiments, —S(O)(NR.sup.a12)R.sup.a13 is
##STR00072##
In some embodiments, R.sup.a12 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a12 is hydrogen or methyl. In some embodiments, R.sup.a13 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a13 is cyclopentyl. In some embodiments, —S(O).sub.2NR.sup.a14R.sup.a15 is
##STR00073## ##STR00074## ##STR00075##
In some embodiments, —S(O).sub.2NR.sup.a14R.sup.a15 is
##STR00076## ##STR00077## ##STR00078##
In some embodiments, —S(O).sub.2NR.sup.a14R.sup.a15 is
##STR00079##
In some embodiments, R.sup.a14 and R.sup.a15 are each independently hydrogen; C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —OH, —O(C.sub.1-6 alkyl), —S(C.sub.1-6 alkyl), and halo; C.sub.2-6 alkenyl; C.sub.3-10 cycloalkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, halo, cyano, —OH, —O(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, —O(C.sub.1-6 alkyl), and halo, wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; C.sub.3-10 cycloalkenyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more C.sub.1-6 alkyl. In some embodiments, R.sup.a14 and R.sup.a15 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a14 is hydrogen and R.sup.a15 is butyl. In some embodiments, R.sup.a15 is tert-butyl. In some embodiments, —S(O).sub.2R.sup.a16 is
##STR00080##
In some embodiments, —S(O).sub.2R.sup.a16 is
##STR00081##
In some embodiments, —S(O).sub.2R.sup.a15 is
##STR00082##
In some embodiments, R.sup.a16 is C.sub.3-10 cycloalkyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.1-6 alkyl or halo. In some embodiments, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20 is —C(O)NR.sup.a19R.sup.a20 or —(CR.sup.a17R.sup.a18)C(O)NR.sup.a19R.sup.a20. In some embodiments, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20 is —C(O)NR.sup.a19R.sup.a20. In some embodiments, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20 is —(CR.sup.a17R.sup.a18)C(O)NR.sup.a19R.sup.a20. In some embodiments, R.sup.a17 and R.sup.a18 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a17 and R.sup.a18 are each hydrogen. In some embodiments, R.sup.a19 and R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a21 is hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more C.sub.3-10 cycloalkyl. In some embodiments, —SR.sup.a21 is
##STR00083##
In some embodiments, R.sup.a22 is hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more C.sub.3-10 cycloalkyl. In some embodiments, —C(O)R.sup.a22 is
##STR00084##
In some embodiments, R.sup.a23 and R.sup.a24 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more C.sub.3-10 cycloalkyl. In some embodiments, —P(O)(R.sup.a23)(R.sup.a24) is
##STR00085##
In some embodiments, R.sup.24 is hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more C.sub.3-10 cycloalkyl. In some embodiments, —C═NR.sup.a25 is
##STR00086##
In some embodiments, Z.sup.1-Z.sup.4 are each independently C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo or C.sub.1-3 alkyl. In some embodiments, Z.sup.1-Z.sup.4 are each independently
##STR00087##
[0163] In some embodiments of Formula (II), Z.sup.6 is 3- to 10-membered heterocycloalkyl. In some embodiments, Z.sup.6 is
##STR00088##
In some embodiments, R.sup.a26 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a27 is hydrogen. In some embodiments, R.sup.a27 and R.sup.a28 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a27 and R.sup.a28 are each independently hydrogen, cyclopropyl, ethyl, or isopropyl. In some embodiments, R.sup.a29 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a29 is hydrogen. In some embodiments, R.sup.a30 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a30 is tert-butyl. In some embodiments, —N═S(O)R.sup.a31R.sup.a32 is
##STR00089##
In some embodiments, R.sup.a31 and R.sup.a32 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a31 and R.sup.a32 are each independently methyl or cyclopentyl. In some embodiments, —S(O)R.sup.a33 is
##STR00090##
In some embodiments, R.sup.a33 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a33 is cyclopentyl. In some embodiments, —S(O)(NR.sup.a34)R.sup.a35 is
##STR00091##
In some embodiments, R.sup.a34 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a34 is hydrogen or methyl. In some embodiments, R.sup.a35 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a35 is cyclopentyl. In some embodiments, —S(O).sub.2NR.sup.a34R.sup.a35 is
##STR00092## ##STR00093## ##STR00094##
In some embodiments, —S(O).sub.2NR.sup.a34R.sup.a35 is
##STR00095##
In some embodiments, —S(O).sub.2NR.sup.a34R.sup.a35 is
##STR00096## ##STR00097## ##STR00098##
In some embodiments, R.sup.a36 and R.sup.a37 are each independently hydrogen; C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —OH, —O(C.sub.1-6 alkyl), —S(C.sub.1-6 alkyl), and halo; C.sub.2-6 alkenyl; C.sub.3-10 cycloalkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, halo, cyano, —OH, —O(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of —OH, —O(C.sub.1-6 alkyl), and halo, wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; C.sub.3-10 cycloalkenyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more C.sub.1-6 alkyl. In some embodiments, R.sup.a36 and R.sup.a37 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.a36 is hydrogen and R.sup.a37 is butyl. In some embodiments, R.sup.a37 is tert-butyl. In some embodiments, —S(O).sub.2R.sup.a3 is
##STR00099##
In some embodiments, —S(O).sub.2R.sup.a38 is
##STR00100## ##STR00101##
In some embodiments, —S(O).sub.2R.sup.a38 is
##STR00102##
In some embodiments, R.sup.a38 is C.sub.3-10 cycloalkyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of C.sub.1-6 alkyl or halo. In some embodiments, —SR.sup.a39 is
##STR00103##
In some embodiments, R.sup.a39 is C.sub.3-10 cycloalkyl. In some embodiments, R.sup.a40 is C.sub.3-10cycloalkyl. In some embodiments, —C(O)R.sup.a40 is
##STR00104##
In some embodiments, —CH(Z.sup.7)(Z.sup.8), wherein Z.sup.7 is hydrogen or —OH, and Z.sup.8 is C.sub.1-6 alkyl, C.sub.3-10 cycloalkyl optionally substituted with one or more halo, or 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo. In some embodiments, Z.sup.7 is —OH. In some embodiments, Z.sup.7 is H. In some embodiments, Z.sup.8 is C.sub.1-6 alkyl. In some embodiments, Z.sup.8 is C.sub.3-10 cycloalkyl optionally substituted with one ore more halo. In some embodiments, Z.sup.8 is 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo. In some embodiments, —CH(Z.sup.7)(Z.sup.8) is
##STR00105##
[0164] In some embodiments of Formula (II), Z.sup.1, Z.sup.2, Z.sup.3, and Z.sup.4 are each independently selected from the group consisting of fluoro, chloro, —OH, amino, —CH.sub.2OH,
##STR00106## ##STR00107## ##STR00108## ##STR00109## ##STR00110## ##STR00111##
In some embodiments, Z.sup.1, Z.sup.2, Z.sup.3, and Z.sup.4 are each independently selected from the group consisting of —CH.sub.2OH,
##STR00112## ##STR00113##
In some embodiments, ring A is bi-substituted phenyl. In some embodiments, ring A is selected from the group consisting of
##STR00114## ##STR00115##
[0165] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon. In some embodiments, ring B is C.sub.5-7 cycloalkyl. In some embodiments, ring B is cyclopentyl, cyclohexyl, or cycloheptyl. In some embodiments, ring B is
##STR00116##
wherein * denotes the point of attachment to the rest of Formula (II). In some embodiments, ring B is C.sub.5-7 cycloalkenyl. In some embodiments, ring B is cyclopentenyl, cyclohexenyl, or cycloheptenyl. In some embodiments, ring B is
##STR00117##
wherein * denotes the point of attachment to the rest of Formula (II). In some embodiments, ring B is
##STR00118##
wherein * denotes the point of attachment to the rest of Formula (II). In some embodiments, ring B is 5- to 7-membered heterocycloalkyl. In some embodiments, ring B is 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon. In some embodiments, ring B is tetrahydrofuranyl or 1,3-dioxanyl. In some embodiments, ring B is
##STR00119##
wherein * denotes the point of attachment to the rest of Formula (II).
[0166] In some embodiments of Formula (II), ring B is substituted with m R.sup.B groups, wherein each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl. In some embodiment, an R.sup.B group is methyl or ethyl. In some embodiment, two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form cyclopropyl. In some embodiments, two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form cyclopropyl.
[0167] In some embodiments of Formula (II), m is 0, 1, 2, 3, or 4. In some embodiments, m is 0, 1, 2, or 3. In some embodiments, m is 0, 1, or 2. In some embodiments, m is 0 or 1. In some embodiments, m is 0. In some embodiments, m is 1.
[0168] In some embodiments,
##STR00120##
of Formula (II) is
[0169] ##STR00121##
wherein * denotes the point of attachment to the rest of Formula (II). In some embodiments,
##STR00122##
of Formula (II) is
[0170] ##STR00123##
or wherein * denotes the point of attachment to the rest of Formula (II). In some embodiments,
##STR00124##
is
##STR00125##
wherein of * denotes the point of attachment to the rest of Formula (II).
[0171] In some embodiments of Formula (II), or a pharmaceutically acceptable salt thereof, Y is Nor CR.sup.C1. Y.sup.2 is N or CR.sup.C2; Y.sup.3 is N or CR.sup.C3; and Y.sup.4 is N or CR.sup.C4. In some embodiments, no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N. In some embodiments, no more than two of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N. In some embodiments, no more than one of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 is N. In some embodiments, Y.sup.1 is CR.sup.C1. Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4. In some embodiments, Y.sup.1 is N; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4. In some embodiments, Y.sup.1 is CR.sup.C1. Y.sup.2 is N; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
[0172] In some embodiments of Formula (II), R.sup.C1-R.sup.C4 are each independently hydrogen or R.sup.F, wherein R.sup.F is halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, —O—S(O).sub.2R.sup.c19, or C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of halo and —OH.
[0173] In some embodiments of Formula (II), R.sup.C1 is hydrogen or halo. In some embodiments, R.sup.C1 is hydrogen or fluoro. In some embodiments, R.sup.C3 is hydrogen. In some embodiments, R.sup.C4 is hydrogen or —NH.sub.2. In some embodiments, R.sup.C1, R.sup.C3, and R.sup.C4 are each independently hydrogen, halo, or —NH.sub.2.
[0174] In some embodiments of Formula (II), R.sup.C2 is cyano, —OH, —CH.sub.2OH, fluoro, bromo, —NO.sub.2,
##STR00126##
In some embodiments, R.sup.C2 is cyano, —OH, —CH.sub.2OH, bromo, —NO.sub.2,
##STR00127##
In some embodiments, R.sup.C2 is
##STR00128##
In some embodiments, R.sup.C2 is cyano, —OH, halo, —NO.sub.2, C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13—NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.C2 is cyano, —OH, halo, —NO.sub.2, C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13—NR.sup.c14C(O)OR.sup.c15, or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from the group consisting of halo and —OH. In some embodiments, R.sup.C2 is —O—S(O).sub.2R.sup.c19.
[0175] In some embodiments, —C(O)NR.sup.c1R.sup.c2 is
##STR00129##
In some embodiments, R.sup.c1 and R.sup.c2 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c1 and R.sup.c2 are each independently hydrogen, methyl, or ethyl. In some embodiments, —NR.sup.c3R.sup.c4 is
##STR00130##
In some embodiments, R.sup.c3 and R.sup.c4 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c1 and R.sup.c2 are each independently hydrogen, methyl, or ethyl. In some embodiments, —NR.sup.c5S(O).sub.2R.sup.c6 is
##STR00131##
In some embodiments, —NR.sup.c5S(O).sub.2R.sup.c6 is
##STR00132##
In some embodiments, R.sup.c5 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c5 is hydrogen, methyl, or ethyl. In some embodiments, R.sup.c6 is hydrogen or C.sub.1-6 alkyl optionally substituted with one, two, three, four, five, or more substituents independently selected from halo, —OH, —O(C.sub.1-6 alkyl), and —NHC(O)(C.sub.1-6 alky). In some embodiments, R.sup.c5 is methyl or —CH.sub.2CH.sub.2OH. In some embodiments, R.sup.c5 is hydrogen. In some embodiments, R.sup.c6 is ethyl. In some embodiments, R.sup.C6 is —CH.sub.2CH.sub.2F. In some embodiments, R.sup.c6 is —OCH.sub.3. In some embodiments, —P(O)R.sup.c7R.sup.c8 is
##STR00133##
In some embodiments, R.sup.c7 and R.sup.c8 are each independently C.sub.1-6 alkyl. In some embodiments, R.sup.c7 and R.sup.c8 are each methyl. In some embodiments, —N═S(O)R.sup.c9R.sup.c10 is
##STR00134##
In some embodiments, R.sup.c9 and R.sup.c10 are each independently C.sub.1-6 alkyl. In some embodiments, R.sup.c9 and R.sup.c10 are each methyl. In some embodiments, —S(O)(NR.sup.c11)R.sup.c12 is
##STR00135##
In some embodiments, R.sup.c11 is hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c11 is hydrogen or methyl. In some embodiments, R.sup.c12 is C.sub.1-6 alkyl or C.sub.3-10 cycloalkyl. In some embodiments, R.sup.c12 is cyclopropyl. In some embodiments, —S(O).sub.2R.sup.c13 is
##STR00136##
In some embodiments, R.sup.c13 is C.sub.1-6 alkyl. In some embodiments, R.sup.c13 is methyl. In some embodiments, NR.sup.c14C(O)OR.sup.c15 is
##STR00137##
In some embodiments, R.sup.c14 and R.sup.c15 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c14 is hydrogen. In some embodiments, R.sup.c15 is ethyl. In some embodiments, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18 is
##STR00138##
In some embodiments, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18 is —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-3NR.sup.c17C(O)R.sup.c18. In some embodiments, R.sup.c16, R.sup.c17 and R.sup.c18 are each independently hydrogen or C.sub.1-6 alkyl. In some embodiments, R.sup.c16 and R.sup.c17 are hydrogen. In some embodiments, R.sup.c18 is methyl.
[0176] In some embodiments, provided herein are compounds and pharmaceutically acceptable salts thereof described in Table 1.
TABLE-US-00001 TABLE 1 Compound No. Structure Name Compound 1
[0177] In some embodiments, provided herein are compounds and salts thereof described in Table 2. In some embodiments, compounds described herein are not compounds of Table 2.
TABLE-US-00002 TABLE 2 Compound No. Structure Name Compound 1’
[0178] In some variations, any of the compounds described herein, such as a compound of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2), or (II), or any variation thereof, or a compound of Table 1 or 2 may be deuterated (e.g., a hydrogen atom is replaced by a deuterium atom). In some of these variations, the compound is deuterated at a single site. In other variations, the compound is deuterated at multiple sites. Deuterated compounds can be prepared from deuterated starting materials in a manner similar to the preparation of the corresponding non-deuterated compounds. Hydrogen atoms may also be replaced with deuterium atoms using other method known in the art.
[0179] Any formula given herein, such as Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2), or (II), is intended to represent compounds having structures depicted by the structural formula as well as certain variations or forms. In particular, compounds of any formula given herein may have asymmetric centers and therefore exist in different enantiomeric or diastereomeric forms. All optical isomers and stereoisomers of the compounds of the general formula, and mixtures thereof in any ratio, are considered within the scope of the formula. Thus, any formula given herein is intended to represent a racemate, one or more enantiomeric forms, one or more diastereomeric forms, one or more atropisomeric forms, and mixtures thereof in any ratio. Furthermore, certain structures may exist as geometric isomers (i.e., cis and trans isomers), as tautomers, or as atropisomers. Additionally, any formula given herein is intended to refer also to any one of hydrates, solvates, and amorphous and polymorphic forms of such compounds, and mixtures thereof, even if such forms are not listed explicitly. In some embodiments, the solvent is water and the solvates are hydrates.
[0180] Representative examples of compounds detailed herein, including intermediates and final compounds, are depicted in the tables and elsewhere herein. It is understood that in one aspect, any of the compounds may be used in the methods detailed herein, including, where applicable, intermediate compounds that may be isolated and administered to an individual.
[0181] The compounds depicted herein may be present as salts even if salts are not depicted, and it is understood that the compositions and methods provided herein embrace all salts and solvates of the compounds depicted here, as well as the non-salt and non-solvate form of the compound, as is well understood by the skilled artisan. In some embodiments, the salts of the compounds provided herein are pharmaceutically acceptable salts.
[0182] In one variation, the compounds herein are synthetic compounds prepared for administration to an individual. In another variation, compositions are provided containing a compound in substantially pure form. In another variation, provided are pharmaceutical compositions comprising a compound detailed herein and a pharmaceutically acceptable carrier. In another variation, methods of administering a compound are provided. The purified forms, pharmaceutical compositions and methods of administering the compounds are suitable for any compound or form thereof detailed herein.
[0183] Any variation or embodiment of ring A, ring B, ring C, R.sup.a1, R.sup.a2, R.sup.a3, R.sup.a4, R.sup.a5, R.sup.a6, R.sup.a7, R.sup.a8, R.sup.a9, R.sup.a10, R.sup.a11, R.sup.a12, R.sup.a13, R.sup.a14, R.sup.a15, R.sup.a16, R.sup.a17, R.sup.a18, R.sup.a19, R.sup.a20, R.sup.a21, R.sup.a22, R.sup.a23, R.sup.a24, R.sup.a25, R.sup.a26, R.sup.a27, R.sup.a28, R.sup.a29, R.sup.a30, R.sup.a31, R.sup.a32, R.sup.a33, R.sup.a34, R.sup.a35, R.sup.a36, R.sup.a37, R.sup.a38, R.sup.a39, R.sup.a40, R.sup.1a1, R.sup.1a2, R.sup.1a3, R.sup.1a4, R.sup.B, m, X, Y.sup.1, Y.sup.2, Y.sup.3, Y.sup.4, Z.sup.1, Z.sup.2, Z.sup.3, Z.sup.4, Z.sup.5, Z.sup.6, Z.sup.7, Z.sup.8, R.sup.C1, R.sup.C2, R.sup.C3, R.sup.C4, R.sup.c1, R.sup.c2, R.sup.c3, R.sup.c4, R.sup.c5, R.sup.c6, R.sup.c7, R.sup.c8, R.sup.c9, R.sup.c10, R.sup.c11, R.sup.c12, R.sup.c13, R.sup.c14, R.sup.c15, R.sup.c16, R.sup.c17, R.sup.c18, R.sup.c19, R.sup.D, R.sup.E, or R.sup.F provided herein can be combined with every other variation or embodiment of ring A, ring B, ring C, R.sup.a1, R.sup.a2, R.sup.a3, R.sup.a4, R.sup.a5, R.sup.a6, R.sup.a7, R.sup.a8, R.sup.a9, R.sup.a10, R.sup.a11, R.sup.a12, R.sup.a13, R.sup.a14, R.sup.a15, R.sup.a16, R.sup.a17, R.sup.a18, R.sup.a19, R.sup.a20, R.sup.a21, R.sup.a22, R.sup.a23, R.sup.a24, R.sup.a25, R.sup.a26, R.sup.a27, R.sup.a28, R.sup.a29, R.sup.a30, R.sup.a31, R.sup.a32, R.sup.a33, R.sup.a34, R.sup.a35, R.sup.a36, R.sup.a37, R.sup.a38, R.sup.a39, R.sup.a40, R.sup.1a1, R.sup.1a2, R.sup.1a3, R.sup.1a4, R.sup.B, m, X, Y, Y.sup.2, Y.sup.3, Y.sup.4, Z.sup.1, Z.sup.2, Z.sup.3, Z.sup.4, Z.sup.5, Z.sup.6, Z.sup.7, Z.sup.8, R.sup.C1, R.sup.C2, R.sup.C3, R.sup.C4, R.sup.c1, R.sup.c2, R.sup.c3, R.sup.c4, R.sup.c5, R.sup.c6, R.sup.c7, R.sup.c8, R.sup.c9, R.sup.c10, R.sup.c11, R.sup.c12, R.sup.c13, R.sup.c14, R.sup.c15, R.sup.c16, R.sup.c17, R.sup.c18, R.sup.c19, R.sup.D, R.sup.E, or R.sup.F, the same as if each and every combination had been individually and specifically described.
[0184] As used herein, when any variable occurs more than one time in a chemical formula, its definition on each occurrence is independent of its definition at every other occurrence.
[0185] Compound names provided herein, including in Table 1 and Table 2, are provided by Chemaxon Marvin Structure to Name 20 or ChemDraw Professional 20. One of skilled in the art would understand that the compounds may be named or identified using various commonly recognized nomenclature systems and symbols. By way of example, the compounds may be named or identified with common names, systematic or non-systematic names. The nomenclature systems and symbols that are commonly recognized in the art of chemistry include, for example, Chemical Abstract Service (CAS), ChemBioDraw Ultra, and International Union of Pure and Applied Chemistry (IUPAC).
Compositions
[0186] Also provided are compositions, such as pharmaceutical compositions, that include a compound disclosed and/or described herein and one or more additional medicinal agents, pharmaceutical agents, adjuvants, carriers, excipients, and the like. Suitable medicinal and pharmaceutical agents include those described herein. In some embodiments, the pharmaceutical composition includes a pharmaceutically acceptable excipient or adjuvant and at least one chemical entity as described herein. Examples of pharmaceutically acceptable excipients include, but are not limited to, mannitol, lactose, starch, magnesium stearate, sodium saccharine, talcum, cellulose, sodium crosscarmellose, glucose, gelatin, sucrose, and magnesium carbonate. In some embodiments, provided are compositions, such as pharmaceutical compositions that contain one or more compounds described herein, or a pharmaceutically acceptable salt thereof.
[0187] In some embodiments, provided is a pharmaceutically acceptable composition comprising a compound of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2), or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof. In some aspects, a composition may contain a synthetic intermediate that may be used in the preparation of a compound described herein. The compositions described herein may contain any other suitable active or inactive agents.
[0188] Any of the compositions described herein may be sterile or contain components that are sterile. Sterilization can be achieved by methods known in the art. Any of the compositions described herein may contain one or more compounds that are substantially pure.
[0189] Also provided are packaged pharmaceutical compositions, comprising a pharmaceutical composition as described herein and instructions for using the composition to treat a patient suffering from a disease or condition described herein.
Methods of Use
[0190] As described herein, the compounds of the present disclosure are inhibitors of KIF18A. In one aspect, the compounds and pharmaceutical compositions herein may be used to inhibit KIF18A. In another aspect, the compounds and pharmaceutical compositions herein may be used to treat or prevent a disease or condition in an individual.
[0191] The inhibitory activity of the compounds described herein against KIF18A may be determined and measured by methods known in the art including, but not limited to, inhibition of ATP hydrolysis in the presence of microtubules (Hackney D. D., Jiang W. (2001) Assays for Kinesin Microtubule-Stimulated ATPase Activity. In: Vernos I. (eds) Kinesin Protocols. Methods in Molecular Biology™, vol 164. Humana Press. https://doi.org/10.1385/1-59259-069-1:65).
[0192] In one aspect, provided herein is a method of inhibiting KIF18A comprising contacting a cell with an effective amount of a compound or a pharmaceutical composition as described herein. In some embodiments, provided herein are methods of inhibiting KIF18A comprising contacting a cell with an effective amount of a compound of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof. In some embodiments, provided herein are methods of inhibiting KIF18A comprising contacting a cell with an effective amount of a pharmaceutical composition comprising a compound of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II) or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof. In one variations of the aforementioned embodiments, the cell is contacted in vitro. In other variations of the aforementioned embodiments, the cell is contacted in vivo.
[0193] In another aspect, the compounds and pharmaceutical compositions herein may be used to treat or prevent a disease or condition in an individual, comprising administering an effective amount of a compound or a pharmaceutical composition as described herein. When used in a prophylactic manner, the compounds disclosed and/or described herein may prevent a disease or disorder from developing in an individual at risk of developing the disease or disorder, or lessen the extent of a disease or disorder that may develop.
[0194] In some embodiments, provided herein are methods of treating or preventing a disease or condition in an individual, comprising administering to the subject a therapeutically effective amount of a compound or a pharmaceutical composition as described herein. In some embodiments, provided herein are methods of treating or preventing a disease or condition in an individual, comprising administering to the subject a therapeutically effective amount of a compound Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof. In some embodiments, provided herein are methods of treating or preventing a disease or condition in an individual, comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a compound a compound Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof.
[0195] In some embodiments, the disease or condition is mediated by KIF18A. In some embodiments, the disease or condition is cancer. In some embodiments, the disease or condition is a cellular proliferation disorder, including uncontrolled cell growth, aberrant cell cycle regulation, centrosome abnormalities (structural and or numeric, fragmentation), a solid tumor, hematopoietic cancer and hyperproliferative disorder, such as thyroid hyperplasia (especially Grave's disease), and cyst (such as hypervascularity of ovarian stroma, characteristic of polycystic ovarian syndrome (Stein-Leventhal syndrome). Solid and hematologically derived tumors, such as carcinomas, may include but are not limited to cancer of the anus, bladder, breast, colon, small intestine, appendix, kidney, renal pelvis, ureter, urothelium, liver, lung (including squamous cell and small cell lung cancer), pleura, esophagus, head and neck, nasopharynx, oropharynx, hypopharynx, oral cavity, larynx, biliary tract, gall-bladder, ovary, testicle, germ cell, uterus, pancreas, stomach, cervix, thyroid, prostate, salivary gland, and skin (including squamous cell carcinoma), hematopoietic tumors of lymphoid lineage (including leukemia, acute lymphocitic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T-cell-lymphoma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, hairy cell lymphoma and Burkett's lymphoma), hematopoietic tumors of myeloid lineage (including acute and chronic myelogenous leukemias, myelodysplastic syndrome and promyelocytic leukemia), hematopoietic tumors of any lineage, myeloma, tumors of mesenchymal origin (including fibrosarcoma and rhabdomyosarcoma, and other sarcomas, e.g., soft tissue and bone), tumors of the central and peripheral nervous system (including astrocytoma, neuroblastoma, glioma and schwannomas), tumor of neuroendocrine origin, tumor of endocrine origin, small cell tumors, tumors of unknown primary, other tumors (including retinoblastoma, melanoma, seminoma, teratocarcinoma, osteosarcoma, xenoderoma pigmentosum, keratoctanthoma, thyroid follicular cancer, Ewing's sarcoma, Kaposi's sarcoma), and other cancer-related disorders that are a consequence of cancer presence or progression such as tumor-induced pleural or pericardial effusions, and malignant ascites.
[0196] In some embodiments, provided are methods of treating or preventing cancer in an individual, comprising administering to the individual in need thereof a compound of Formula Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof. In some embodiments, provided are methods of treating or preventing cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of at least one chemical entity as described herein. Also provided herein is the use of a compound of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for treatment of a disease in a subject.
[0197] In some embodiments, provided herein are methods of treating cancer, comprising administering to an individual in need thereof a compound of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof. Also provided herein is the use of a compound of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2) or (II), or a compound of Table 1 or 2, or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for treatment of a cancer.
[0198] In some embodiments, provided herein are methods of treating a disease or condition mediated by KIF18A in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound or a pharmaceutical composition as described herein.
[0199] In some embodiments, provided herein are methods of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound or a pharmaceutical composition as described herein. In some embodiments, the cancer is selected from the group consisting of carcinomas, cancer of the anus, bladder, breast, colon, small intestine, appendix, kidney, renal pelvis, ureter, urothelium, liver, lung, pleura, esophagus, head and neck, nasopharynx, oropharynx, hypopharynx, oral cavity, larynx, biliary tract, gall-bladder, ovary, testicle, germ cell, uterus, pancreas, stomach, cervix, thyroid, prostate, salivary gland, or skin, hematopoietic tumors of lymphoid lineage, hematopoietic tumors of myeloid lineage, hematopoietic tumors of any lineage, myeloma, tumors of mesenchymal origin including sarcomas, tumors of the central and peripheral nervous system, tumor of neuroendocrine origin, tumor of endocrine origin, small cell tumors, tumors of unknown primary, other tumors comprising retinoblastoma, melanoma, seminoma, teratocarcinoma, osteosarcoma, and other cancer-related disorders that are a consequence of cancer presence or progression.
Dosages
[0200] The compounds and compositions disclosed and/or described herein are administered at a therapeutically effective dosage, e.g., a dosage sufficient to provide treatment for the disease state. While human dosage levels have yet to be optimized for the chemical entities described herein, generally, a daily dose ranges from about 0.01 to 100 mg/kg of body weight; in some embodiments, from about 0.05 to 10.0 mg/kg of body weight, and in some embodiments, from about 0.10 to 1.4 mg/kg of body weight. Thus, for administration to a 70 kg person, in some embodiments, the dosage range would be about from 0.7 to 7000 mg per day; in some embodiments, about from 3.5 to 700.0 mg per day, and in some embodiments, about from 7 to 100.0 mg per day. The amount of the chemical entity administered will be dependent, for example, on the subject and disease state being treated, the severity of the affliction, the manner and schedule of administration and the judgment of the prescribing physician. For example, an exemplary dosage range for oral administration is from about 5 mg to about 500 mg per day, and an exemplary intravenous administration dosage is from about 5 mg to about 500 mg per day, each depending upon the compound pharmacokinetics.
[0201] Administration of the compounds and compositions disclosed and/or described herein can be via any accepted mode of administration for therapeutic agents including, but not limited to, oral, sublingual, subcutaneous, parenteral, intravenous, intranasal, topical, transdermal, intraperitoneal, intramuscular, intrapulmonary, vaginal, rectal, or intraocular administration. In some embodiments, the compound or composition is administered orally or intravenously. In some embodiments, the compound or composition disclosed and/or described herein is administered orally.
[0202] Pharmaceutically acceptable compositions include solid, semi-solid, liquid and aerosol dosage forms, such as tablet, capsule, powder, liquid, suspension, suppository, and aerosol forms. The compounds disclosed and/or described herein can also be administered in sustained or controlled release dosage forms (e.g., controlled/sustained release pill, depot injection, osmotic pump, or transdermal (including electrotransport) patch forms) for prolonged timed, and/or pulsed administration at a predetermined rate. In some embodiments, the compositions are provided in unit dosage forms suitable for single administration of a precise dose.
[0203] The compounds disclosed and/or described herein can be administered either alone or in combination with one or more conventional pharmaceutical carriers or excipients (e.g., mannitol, lactose, starch, magnesium stearate, sodium saccharine, talcum, cellulose, sodium crosscarmellose, glucose, gelatin, sucrose, magnesium carbonate). If desired, the pharmaceutical composition can also contain minor amounts of nontoxic auxiliary substances such as wetting agents, emulsifying agents, solubilizing agents, pH buffering agents and the like (e.g., sodium acetate, sodium citrate, cyclodextrine derivatives, sorbitan monolaurate, triethanolamine acetate, triethanolamine oleate). Generally, depending on the intended mode of administration, the pharmaceutical composition will contain about 0.005% to 95%, or about 0.5% to 50%, by weight of a compound disclosed and/or described herein. Actual methods of preparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa.
[0204] In some embodiments, the compositions will take the form of a pill or tablet and thus the composition may contain, along with a compounds disclosed and/or described herein, one or more of a diluent (e.g., lactose, sucrose, dicalcium phosphate), a lubricant (e.g., magnesium stearate), and/or a binder (e.g., starch, gum acacia, polyvinylpyrrolidine, gelatin, cellulose, cellulose derivatives). Other solid dosage forms include a powder, marume, solution or suspension (e.g., in propylene carbonate, vegetable oils or triglycerides) encapsulated in a gelatin capsule.
[0205] Liquid pharmaceutically administrable compositions can, for example, be prepared by dissolving, dispersing or suspending etc. a compound disclosed and/or described herein and optional pharmaceutical additives in a carrier (e.g., water, saline, aqueous dextrose, glycerol, glycols, ethanol or the like) to form a solution or suspension. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, as emulsions, or in solid forms suitable for dissolution or suspension in liquid prior to injection. The percentage of the compound contained in such parenteral compositions depends, for example, on the physical nature of the compound, the activity of the compound and the needs of the subject. However, percentages of active ingredient of 0.01% to 10% in solution are employable, and may be higher if the composition is a solid which will be subsequently diluted to another concentration. In some embodiments, the composition will comprise from about 0.2 to 2% of a compound disclosed and/or described herein in solution.
[0206] Pharmaceutical compositions of the compounds disclosed and/or described herein may also be administered to the respiratory tract as an aerosol or solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose. In such a case, the particles of the pharmaceutical composition may have diameters of less than 50 microns, or in some embodiments, less than 10 microns.
[0207] In addition, pharmaceutical compositions can include a compound disclosed and/or described herein and one or more additional medicinal agents, pharmaceutical agents, adjuvants, and the like. Suitable medicinal and pharmaceutical agents include those described herein.
Kits
[0208] Also provided are articles of manufacture and kits containing any of the compounds or pharmaceutical compositions provided herein. The article of manufacture may comprise a container with a label. Suitable containers include, for example, bottles, vials, and test tubes. The containers may be formed from a variety of materials such as glass or plastic. The container may hold a pharmaceutical composition provided herein. The label on the container may indicate that the pharmaceutical composition is used for preventing, treating or suppressing a condition described herein, and may also indicate directions for either in vivo or in vitro use.
[0209] In one aspect, provided herein are kits containing a compound or composition described herein and instructions for use. The kits may contain instructions for use in the treatment of any disease or condition described herein in an individual in need thereof. A kit may additionally contain any materials or equipment that may be used in the administration of the compound or composition, such as vials, syringes, or IV bags. A kit may also contain sterile packaging.
Combinations
[0210] The compounds and compositions described and/or disclosed herein may be administered alone or in combination with other therapies and/or therapeutic agents useful in the treatment of the aforementioned disorders.
[0211] The compounds and compositions described and/or disclosed herein may be combined with one or more other therapies to treat the diseases or conditions described herein. In some embodiments, the disease or condition is cancer. In some embodiments, the disease or condition is a cellular proliferation disorder, including uncontrolled cell growth, aberrant cell cycle regulation, centrosome abnormalities (structural and or numeric, fragmentation), a solid tumor, hematopoietic cancer and hyperproliferative disorder, such as thyroid hyperplasia (especially Grave's disease), and cyst (such as hypervascularity of ovarian stroma, characteristic of polycystic ovarian syndrome (Stein-Leventhal syndrome). Solid and hematologically derived tumors, such as carcinomas, may include but are not limited to cancer of the anus, bladder, breast, colon, small intestine, appendix, kidney, renal pelvis, ureter, urothelium, liver, lung (including squamous cell and small cell lung cancer), pleura, esophagus, head and neck, nasopharynx, oropharynx, hypopharynx, oral cavity, larynx, biliary tract, gall-bladder, ovary, testicle, germ cell, uterus, pancreas, stomach, cervix, thyroid, prostate, salivary gland, and skin (including squamous cell carcinoma), hematopoietic tumors of lymphoid lineage (including leukemia, acute lymphocitic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T-cell-lymphoma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, hairy cell lymphoma and Burkett's lymphoma), hematopoietic tumors of myeloid lineage (including acute and chronic myelogenous leukemias, myelodysplastic syndrome and promyelocytic leukemia), hematopoietic tumors of any lineage, myeloma, tumors of mesenchymal origin (including fibrosarcoma and rhabdomyosarcoma, and other sarcomas, e.g., soft tissue and bone), tumors of the central and peripheral nervous system (including astrocytoma, neuroblastoma, glioma and schwannomas), tumor of neuroendocrine origin, tumor of endocrine origin, small cell tumors, tumors of unknown primary, other tumors (including retinoblastoma, melanoma, seminoma, teratocarcinoma, osteosarcoma, xenoderoma pigmentosum, keratoctanthoma, thyroid follicular cancer, Ewing's sarcoma, Kaposi's sarcoma), and other cancer-related disorders that are a consequence of cancer presence or progression such as tumor-induced pleural or pericardial effusions, and malignant ascites.
General Synthetic Methods
[0212] Compounds of Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2), or (II) will now be described by reference to illustrative synthetic schemes for their general preparation below and the specific examples that follow. Artisans will recognize that, to obtain the various compounds herein, starting materials may be suitably selected so that the ultimately desired substituents will be carried through the reaction scheme with or without protection as appropriate to yield the desired product. Alternatively, it may be necessary or desirable to employ, in the place of the ultimately desired substituent, a suitable group that may be carried through the reaction scheme and replaced as appropriate with the desired substituent. In addition, one of skill in the art will recognize that protecting groups may be used to protect certain functional groups (amino, carboxy, or side chain groups) from reaction conditions, and that such groups are removed under standard conditions when appropriate. Unless otherwise specified, the variables are as defined above in reference to Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2), or (II).
[0213] Where it is desired to obtain a particular enantiomer of a compound, this may be accomplished from a corresponding mixture of enantiomers using any suitable conventional procedure for separating or resolving enantiomers. Thus, for example, diastereomeric derivatives may be produced by reaction of a mixture of enantiomers, e.g., a racemate, and an appropriate chiral compound. The diastereomers may then be separated by any convenient means, for example by crystallization and the desired enantiomer recovered. In another resolution process, a racemate may be separated using chiral High Performance Liquid Chromatography. Alternatively, if desired a particular enantiomer may be obtained by using an appropriate chiral intermediate in one of the processes described.
[0214] Chromatography, recrystallization and other conventional separation procedures may also be used with intermediates or final products where it is desired to obtain a particular isomer of a compound or to otherwise purify a product of a reaction.
[0215] General methods of preparing compounds described herein are depicted in exemplified methods below. Variable groups in the schemes provided herein are defined as for Formula (I), (I-1), (I-2), (I-3), (Ia1), (Ia2), or (II), or any variation thereof. Other compounds described herein may be prepared by similar methods.
[0216] In some embodiments, compounds provided herein may be synthesized according to Scheme 1, Scheme 2, Scheme 3, and/or Scheme 4. Ring A, Ring B, Y.sup.1, Y.sup.2, Y.sup.3, Y.sup.4, m, R.sup.B and R.sup.C, as shown in Schemes 1-4 below, are as defined for the compounds of Formula I.
##STR00566##
[0217] Scheme 1 outlines an exemplary route to the synthesis of compound of general formula I. Compounds of formula I are prepared by the reaction of a carboxylic acid of formula A (e.g., X═OH) and an indoline of formula B in the presence of coupling reagent, such as HATU with a base such as iPr2NEt, or EDCI with a HOBt or DMAP. Alternatively, an acid halide of formula A (e.g., X═Cl or F) is reacted directly with the compound of formula B with an acid scavenger, such as Et.sub.3N.
##STR00567##
[0218] Indoline intermediates of formula B may be prepared via the Fisher Indole Synthesis as described in Scheme 2. Arylhydrazines of formula C (e.g., formula C-i, formula C-ii, and formula C-iii) are reacted with a Ring B-substituted carbaldehyde of formula D in the presence of acid, followed by reaction with a reducing agent such as NaBH.sub.4, Pd/C and H.sub.2 gas, or Et.sub.3SiH. Arylhydrazines of formula C-i, which are para-mono-substituted, provide indolines of formula B-i, while hydrazines of formula C-ii, which contain at least one meta substituent and are not substituted in the ortho positions, provide a mixture of indolines of formulae B-ii-a and B-ii-b. Arylhydrazines of formula C-iii, that are substituted at one ortho position, provide indolines of formula B-iii.
##STR00568##
[0219] Indolines of formula B may also be prepared via an 3,3-dialkylation method described in Scheme 3. An indole of formula D is reacted with an optionally substituted 3-6 atom aliphatic and heteroaliphatic linear chain with two terminal leaving groups “LG” (formula E). LG may be Cl, Br, I, or sulfonate ester, or another suitable group displaceable by a nucleophile. The transformation may be mediated by a trialkylboron, such as Et.sub.3B, and base, such as potassium t-butoxide. The spiroannulation reaction is followed by a reaction with a reducing agent such as NaBH.sub.4, Pd/C and H.sub.2 gas, or Et.sub.3SiH.
##STR00569##
[0220] Indolines of formula B may also be prepared via the enolate alkylation of an indolin-2-one of formula F. The indolin-2-one of formula F is deprotonated with a strong base, such as butyllithium, sodium hexamethylsilazide, or potassium t-butoxide, and reacted with an optionally substituted 3-6 atom aliphatic and heteroaliphatic linear chain with two terminal leaving groups “LG” (formula E). LG may be Cl, Br, I, or sulfonate ester, or another suitable group displaceable by a nucleophile. This reaction may be mediated by an additive such as tetramethyldiaminoethane or hexamethylphosphorous triamide. The spiroannulation reaction is followed by a reaction with a reducing agent such as LiAlH.sub.4 or borane.
ENUMERATED EMBODIMENTS
[0221] The following enumerated embodiments are representative of some aspects of the invention.
1. A compound of Formula (I)
##STR00570##
or a pharmaceutically acceptable salt thereof, wherein:
[0222] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a15, and —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20;
[0223] R.sup.a1-R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0224] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0225] each R.sup.B group is independently halo, C.sub.1-6 alkyl, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0226] m is 0, 1, 2, 3, or 4;
[0227] Y.sup.1 is N or CR.sup.C1;
[0228] Y.sup.2 is N or CR.sup.C2;
[0229] Y.sup.3 is N or CR.sup.C3;
[0230] Y.sup.4 is N or CR.sup.C4;
[0231] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0232] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12—S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0233] R.sup.c1-R.sup.c13 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
2. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein the compound is not 4′-fluoro-1′-[3-(piperidine-1-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; 3-cyclopropyl-1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; 1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]-3-(propan-2-yl)urea; [4-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]methanol; 4′-fluoro-1′-(1H-indole-5-carbonyl)-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; N-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]pyrimidin-2-amine; 4′-fluoro-1′-[3-(morpholine-4-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; [3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; or salt of any of the foregoing.
3. The compound of embodiment 1 or 2, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted C.sub.6-14 aryl.
4. The compound of embodiment 3, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted phenyl.
5. The compound of embodiment 1 or 2, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted 5- to 10-membered heteroaryl.
6. The compound of embodiment 5, or a pharmaceutically acceptable salt thereof, wherein ring A is indolyl, indazolyl, pyridinyl, thiophenyl, furanyl, pyrazolyl, pyrrolyl, oxazolyl, chromanyl, or quinolinyl, each optionally substituted.
7. The compound of any one of embodiments 1-6, or a pharmaceutically acceptable salt thereof, wherein R.sup.a1 is hydrogen or C.sub.1-6 alkyl; R.sup.a2 and R.sup.a3 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a4 is hydrogen or C.sub.1-6 alkyl; R.sup.a5 is hydrogen or C.sub.1-6 alkyl; R.sup.a6 and R.sup.a7 are each independently hydrogen, C.sub.1-6 alkyl, or 5- to 12-membered heteroaryl optionally substituted with C.sub.1-6 alkyl; R.sup.a8 and R.sup.a9 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a10 is C.sub.3-10 cycloalkyl; R.sup.a11 is C.sub.3-10 cycloalkyl; R.sup.a12 is hydrogen or C.sub.1-6 alkyl; R.sup.a13 is C.sub.3-10 cycloalkyl; R.sup.a16 is C.sub.3-10 cycloalkyl or 3- to 12-membered heterocycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.1-6 alkyl or halo; R.sup.a17 and R.sup.a18 are each independently hydrogen or C.sub.1-6 alkyl; and R.sup.a19 and R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl.
8. The compound of any one of embodiments 1-7, or a pharmaceutically acceptable salt thereof, wherein R.sup.a14 and R.sup.a15 are each independently hydrogen; C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —OH, —O(C.sub.1-6 alkyl), —S(C.sub.1-6 alkyl), and halo; C.sub.2-6 alkenyl; C.sub.3-10 cycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, halo, cyano, —OH, —O(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of —OH, —O(C.sub.1-6 alkyl), and halo, wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; C.sub.3-10 cycloalkenyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one or more C.sub.1-6 alkyl.
9. The compound of any one of embodiments 1-8, or a pharmaceutically acceptable salt thereof, wherein ring A is substituted with one or more substituents independently selected from the group consisting of fluoro, chloro, —OH, methyl, amino,
##STR00571## ##STR00572## ##STR00573## ##STR00574##
10. The compound of any one of embodiments 1-9, or a pharmaceutically acceptable salt thereof, wherein ring B is C.sub.5-7 cycloalkyl.
11. The compound of any one of embodiments 1-9, or a pharmaceutically acceptable salt thereof, wherein ring B is 5- to 7-membered heterocycloalkyl.
12. The compound of any one of embodiments 1-9, or a pharmaceutically acceptable salt thereof, wherein ring B is
##STR00575##
wherein * denotes the point of attachment to the rest of Formula (I).
13. The compound of any one of embodiments 1-9, or a pharmaceutically acceptable salt thereof, wherein
##STR00576##
of Formula (I) is
[0234] ##STR00577##
wherein * denotes the point of attachment to the rest of Formula (I).
14. The compound of any one of embodiments 1-13, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
15. The compound of any one of embodiments 1-13, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is N; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
16. The compound of any one of embodiments 1-13, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is N; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
17. The compound of any one of embodiments 1-16, or a pharmaceutically acceptable salt thereof, wherein R.sup.C1, R.sup.C3, and R.sup.C4 are each independently hydrogen, halo, or —NH.sub.2.
18. The compound of any one of embodiments 1-17, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is cyano, —OH, —CH.sub.2OH, bromo, —NO.sub.2,
##STR00578##
19. The compound of embodiment 1 or 2, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of compounds of Table 1.
20. The compound of embodiment 1, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of compounds of Table 2.
21. A pharmaceutical composition comprising a compound of any one of embodiments 1-18, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
22. A method of inhibiting KIF18A comprising contacting a cell with an effective amount of a compound of any one of embodiments 1-20, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 21.
23. A method of treating a disease or condition mediated by KIF18A in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of any one of embodiments 1-20, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 21.
24. A method of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of any one of embodiments 1-20, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 21.
25. The method of embodiment 24, wherein the cancer is selected from the group consisting of carcinomas, cancer of the anus, bladder, breast, colon, small intestine, appendix, kidney, renal pelvis, ureter, urothelium, liver, lung, pleura, esophagus, head and neck, nasopharynx, oropharynx, hypopharynx, oral cavity, larynx, biliary tract, gall-bladder, ovary, testicle, germ cell, uterus, pancreas, stomach, cervix, thyroid, prostate, salivary gland, or skin, hematopoietic tumors of lymphoid lineage, hematopoietic tumors of myeloid lineage, hematopoietic tumors of any lineage, myeloma, tumors of mesenchymal origin including sarcomas, tumors of the central and peripheral nervous system, tumor of neuroendocrine origin, tumor of endocrine origin, small cell tumors, tumors of unknown primary, other tumors comprising retinoblastoma, melanoma, seminoma, teratocarcinoma, osteosarcoma, and other cancer-related disorders that are a consequence of cancer presence or progression.
26. A compound of Formula (I)
##STR00579##
or a pharmaceutically acceptable salt thereof, wherein:
[0235] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo;
[0236] R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0237] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0238] each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0239] m is 0, 1, 2, 3, or 4;
[0240] Y.sup.1 is N or CR.sup.C1;
[0241] Y.sup.2 is N or CR.sup.C2;
[0242] Y.sup.3 is N or CR.sup.C3;
[0243] Y.sup.4 is N or CR.sup.C4;
[0244] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0245] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0246] R.sup.c1-R.sup.c15 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
27. A compound of Formula (I-1)
##STR00580##
or a pharmaceutically acceptable salt thereof, wherein:
[0247] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, and —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20.
[0248] R.sup.a1-R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0249] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0250] each R.sup.B group is independently halo, C.sub.1-6 alkyl, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0251] m is 0, 1, 2, 3, or 4;
[0252] Y.sup.1 is N or CR.sup.C1;
[0253] Y.sup.2 is N or CR.sup.C2;
[0254] Y.sup.3 is N or CR.sup.C3;
[0255] Y.sup.4 is N or CR.sup.C4;
[0256] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0257] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12—S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0258] R.sup.c1-R.sup.c13 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
28. The compound of embodiment 26 or 27, or a pharmaceutically acceptable salt thereof, wherein the compound is not 4′-fluoro-1′-[3-(piperidine-1-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; 3-cyclopropyl-1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; 1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]-3-(propan-2-yl)urea; [4-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]methanol; 4′-fluoro-1′-(1H-indole-5-carbonyl)-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; N-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]pyrimidin-2-amine; 4′-fluoro-1′-[3-(morpholine-4-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; [3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; or salt of any of the foregoing.
29. The compound of embodiment 26 or 28, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted C.sub.6-14 aryl.
30. The compound of embodiment 29, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted phenyl.
31. The compound of embodiment 26 or 28, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted 5- to 10-membered heteroaryl.
32. The compound of embodiment 31, or a pharmaceutically acceptable salt thereof, wherein ring A is indolyl, indazolyl, pyridinyl, thiophenyl, furanyl, pyrazolyl, pyrrolyl, oxazolyl, chromanyl, or quinolinyl, each optionally substituted.
33. The compound of any one of embodiments 26 and 28-32, or a pharmaceutically acceptable salt thereof, wherein R.sup.a1 is hydrogen or C.sub.1-6 alkyl; R.sup.a2 and R.sup.a3 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a4 is hydrogen or C.sub.1-6 alkyl; R.sup.a5 is hydrogen or C.sub.1-6 alkyl; R.sup.a6 and R.sup.ay are each independently hydrogen, C.sub.1-6 alkyl, or 5- to 12-membered heteroaryl optionally substituted with C.sub.1-6 alkyl; R.sup.as and R.sup.a9 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a10 is C.sub.3-10 cycloalkyl; R.sup.a11 is C.sub.3-10 cycloalkyl; R.sup.a12 is hydrogen or C.sub.1-6 alkyl; R.sup.a13 is C.sub.3-10 cycloalkyl; R.sup.a16 is C.sub.3-10 cycloalkyl or 3- to 12-membered heterocycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.1-6 alkyl or halo; R.sup.a17 and R.sup.a18 are each independently hydrogen or C.sub.1-6 alkyl; R.sup.a19 and R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a21 is C.sub.3-10 cycloalkyl; and R.sup.a22 is C.sub.3-10 cycloalkyl.
34. The compound of any one of embodiments 26 and 28-33, or a pharmaceutically acceptable salt thereof, wherein R.sup.a14 and R.sup.a15 are each independently hydrogen; C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —OH, —O(C.sub.1-6 alkyl), —S(C.sub.1-6 alkyl), and halo; C.sub.2-6 alkenyl; C.sub.3-10 cycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, halo, cyano, —OH, —O(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of —OH, —O(C.sub.1-6 alkyl), and halo, wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; C.sub.3-10 cycloalkenyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one or more C.sub.1-6 alkyl.
35. The compound of any one of embodiments 26 and 28-34, or a pharmaceutically acceptable salt thereof, wherein R.sup.a14 is hydrogen and R.sup.a15 is tert-butyl.
36. The compound of any one of embodiments 26 and 28-35, or a pharmaceutically acceptable salt thereof, wherein ring A is substituted with one or more substituents independently selected from the group consisting of fluoro, chloro, —OH, methyl, amino,
##STR00581## ##STR00582## ##STR00583## ##STR00584##
37. The compound of any one of embodiments 26 and 28-36, or a pharmaceutically acceptable salt thereof, wherein ring A is phenyl substituted with
##STR00585##
38. The compound of any one of embodiments 26 and 28-37, or a pharmaceutically acceptable salt thereof, wherein ring B is C.sub.5-7 cycloalkyl.
39. The compound of any one of embodiments 26 and 28-37, or a pharmaceutically acceptable salt thereof, wherein ring B is 5- to 7-membered heterocycloalkyl.
40. The compound of any one of embodiments 26 and 28-37, or a pharmaceutically acceptable salt thereof, wherein ring B is
##STR00586##
wherein* denotes the point of attachment to the rest of Formula (I).
41. The compound of any one of embodiments 26 and 28-37, or a pharmaceutically acceptable salt thereof, wherein
##STR00587##
of Formula (I) is
[0259] ##STR00588##
wherein * denotes the point of attachment to the rest of Formula (I).
42. The compound of embodiment 41, or a pharmaceutically acceptable salt thereof, wherein
##STR00589##
of Formula (I) is
[0260] ##STR00590##
43. The compound of any one of embodiments 25 and 28-42, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
44. The compound of embodiment 43, or a pharmaceutically acceptable salt thereof, wherein R.sup.C1, R.sup.C3, and R.sup.C4 are each independently hydrogen, halo, or —NH.sub.2.
45. The compound of embodiment 43 or 44, or a pharmaceutically acceptable salt thereof, wherein R.sup.C1, R.sup.C3, and R.sup.C4 are each hydrogen.
46. The compound of any one of embodiments 25 and 28-41, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is N; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.c4.
47. The compound of any one of embodiments 25 and 28-41, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is N; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
48. The compound of any one of embodiments 25 and 28-47, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is cyano, —OH, —CH.sub.2OH, bromo, —NO.sub.2,
##STR00591##
49. The compound of embodiment 48, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is
##STR00592##
50. The compound of embodiment 26 or 28, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of compounds of Table 1.
51. The compound of embodiment 26, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of compounds of Table 2.
52. A pharmaceutical composition comprising a compound of any one of embodiments 26-51, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
53. A method of inhibiting KIF18A comprising contacting a cell with an effective amount of a compound of any one of embodiments 26-51, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 52.
54. A method of treating a disease or condition mediated by KIF18A in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of any one of embodiments 26-51, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 52.
55. A method of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of any one of embodiments 26-51, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 52.
56. The method of embodiment 55, wherein the cancer is selected from the group consisting of carcinomas, cancer of the anus, bladder, breast, colon, small intestine, appendix, kidney, renal pelvis, ureter, urothelium, liver, lung, pleura, esophagus, head and neck, nasopharynx, oropharynx, hypopharynx, oral cavity, larynx, biliary tract, gall-bladder, ovary, testicle, germ cell, uterus, pancreas, stomach, cervix, thyroid, prostate, salivary gland, or skin, hematopoietic tumors of lymphoid lineage, hematopoietic tumors of myeloid lineage, hematopoietic tumors of any lineage, myeloma, tumors of mesenchymal origin including sarcomas, tumors of the central and peripheral nervous system, tumor of neuroendocrine origin, tumor of endocrine origin, small cell tumors, tumors of unknown primary, other tumors comprising retinoblastoma, melanoma, seminoma, teratocarcinoma, osteosarcoma, and other cancer-related disorders that are a consequence of cancer presence or progression.
57. A compound of Formula (I)
##STR00593##
or a pharmaceutically acceptable salt thereof, wherein:
[0261] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo;
[0262] R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1ai and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0263] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0264] each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0265] m is 0, 1, 2, 3, or 4;
[0266] Y.sup.1 is N or CR.sup.C1;
[0267] Y.sup.2 is N or CR.sup.C2;
[0268] Y.sup.3 is N or CR.sup.C3;
[0269] Y.sup.4 is N or CR.sup.C4;
[0270] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0271] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, —NR.sup.c16S(O).sub.2(CH.sub.2).sub.1-6NR.sup.c17C(O)R.sup.c18, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0272] R.sup.c1-R.sup.c18 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
58. A compound of Formula (I-2)
##STR00594##
or a pharmaceutically acceptable salt thereof, wherein:
[0273] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20, —SR.sup.a21, —C(O)R.sup.a22, and C.sub.1-6 alkyl substituted with one or more substituents independently selected from the group consisting of —OH, cyano, C.sub.3-10 cycloalkyl, and 3- to 10-membered heterocycloalkyl optionally substituted with one or more halo;
[0274] R.sup.a1-R.sup.a22 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl, C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0275] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0276] each R.sup.B group is independently halo, C.sub.1-6 alkyl optionally substituted with one or more halo, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0277] m is 0, 1, 2, 3, or 4;
[0278] Y.sup.1 is N or CR.sup.C1;
[0279] Y.sup.2 is N or CR.sup.C2;
[0280] Y.sup.3 is N or CR.sup.C3;
[0281] Y.sup.4 is N or CR.sup.C4;
[0282] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0283] R.sup.C1-R.sup.C4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12, —S(O).sub.2R.sup.c13, —NR.sup.c14C(O)OR.sup.c15, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0284] R.sup.c1-R.sup.c15 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
59. A compound of Formula (I-1)
##STR00595##
or a pharmaceutically acceptable salt thereof, wherein:
[0285] ring A is C.sub.6-14 aryl or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, C.sub.1-6 alkyl, 3- to 10-membered heterocycloalkyl, —NR.sup.a1C(O)NR.sup.a2R.sup.a3, —NR.sup.a4C(O)OR.sup.a5, —NR.sup.a6R.sup.a7, —N═S(O)R.sup.a8R.sup.a9, —OR.sup.a10, —S(O)R.sup.a11, —S(O)(NR.sup.a12)R.sup.a13, —S(O).sub.2NR.sup.a14R.sup.a15, —S(O).sub.2R.sup.a16, and —(CR.sup.a17R.sup.a18).sub.0-1C(O)NR.sup.a19R.sup.a20;
[0286] R.sup.a1-R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, C.sub.3-10 cycloalkenyl, 3- to 10-membered heterocycloalkyl, 3- to 10-membered heterocycloalkenyl C.sub.6-14 aryl, or 5- to 12-membered heteroaryl, each optionally substituted with one or more substituents independently selected from the group consisting of halo, cyano, —OH, —O(C.sub.1-6 alkyl), C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —S(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo, —OH, and —O(C.sub.1-6 alkyl), wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl;
[0287] ring B is C.sub.5-7 cycloalkyl, C.sub.5-7 cycloalkenyl, or 5- to 7-membered heterocycloalkyl wherein one or two of the ring atoms are each oxygen and the remaining ring atoms are each carbon;
[0288] each R.sup.B group is independently halo, C.sub.1-6 alkyl, or C.sub.2-6 alkenyl; or two vicinal R.sup.B groups are taken together with the carbon atoms to which they are attached to form C.sub.3-10 cycloalkyl; or two geminal R.sup.B groups are taken together with the carbon atom to which they are attached to form C.sub.3-10 cycloalkyl;
[0289] m is 0, 1, 2, 3, or 4;
[0290] Y.sup.1 is N or CR.sup.C1;
[0291] Y.sup.2 is N or CR.sup.C2;
[0292] Y.sup.3 is N or CR.sup.C3;
[0293] Y.sup.4 is N or CR.sup.C4;
[0294] wherein no more than three of Y.sup.1, Y.sup.2, Y.sup.3, and Y.sup.4 are N;
[0295] R.sup.C1-R.sup.c4 are each independently hydrogen, halo, cyano, —OH, —NO.sub.2, —C(O)NR.sup.c1R.sup.c2, —NR.sup.c3R.sup.c4, —NR.sup.c5S(O).sub.2R.sup.c6, —P(O)R.sup.c7R.sup.c8, —N═S(O)R.sup.c9R.sup.c10, —S(O)(NR.sup.c11)R.sup.c12—S(O).sub.2R.sup.c13, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH;
[0296] R.sup.c1-R.sup.c13 are each independently hydrogen, C.sub.3-10 cycloalkyl, or C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of halo and —OH.
60. The compound of embodiment 57 or 58, or a pharmaceutically acceptable salt thereof, wherein the compound is not 4′-fluoro-1′-[3-(piperidine-1-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; 3-cyclopropyl-1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; 1-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]-3-(propan-2-yl)urea; [4-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]methanol; 4′-fluoro-1′-(1H-indole-5-carbonyl)-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; N-[3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]pyrimidin-2-amine; 4′-fluoro-1′-[3-(morpholine-4-sulfonyl)benzoyl]-1′,2′-dihydrospiro[cyclopentane-1,3′-indole]; [3-({4′-fluoro-1′,2′-dihydrospiro[cyclopentane-1,3′-indol]-1′-yl}carbonyl)phenyl]urea; or salt of any of the foregoing.
61. The compound of embodiment 57 or 60, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted C.sub.6-14 aryl.
62. The compound of embodiment 61, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted phenyl.
63. The compound of embodiment 57 or 60, or a pharmaceutically acceptable salt thereof, wherein ring A is optionally substituted 5- to 10-membered heteroaryl.
64. The compound of embodiment 63, or a pharmaceutically acceptable salt thereof, wherein ring A is indolyl, indazolyl, pyridinyl, thiophenyl, furanyl, pyrazolyl, pyrrolyl, oxazolyl, chromanyl, or quinolinyl, each optionally substituted.
65. The compound of any one of embodiments 57 and 60-64, or a pharmaceutically acceptable salt thereof, wherein R.sup.a1 is hydrogen or C.sub.1-6 alkyl; R.sup.a2 and R.sup.a3 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a4 is hydrogen or C.sub.1-6 alkyl; R.sup.a5 is hydrogen or C.sub.1-6 alkyl; R.sup.a6 and R.sup.ay are each independently hydrogen, C.sub.1-6 alkyl, or 5- to 12-membered heteroaryl optionally substituted with C.sub.1-6 alkyl; R.sup.as and R.sup.a9 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a10 is C.sub.3-10 cycloalkyl; R.sup.a11 is C.sub.3-10 cycloalkyl; R.sup.a12 is hydrogen or C.sub.1-6 alkyl; R.sup.a13 is C.sub.3-10 cycloalkyl; R.sup.a16 is C.sub.3-10 cycloalkyl or 3- to 12-membered heterocycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.1-6 alkyl or halo; R.sup.a17 and R.sup.a18 are each independently hydrogen or C.sub.1-6 alkyl; R.sup.a19 and R.sup.a20 are each independently hydrogen, C.sub.1-6 alkyl, or C.sub.3-10 cycloalkyl; R.sup.a21 is C.sub.3-10 cycloalkyl; and R.sup.a22 is C.sub.3-10 cycloalkyl.
66. The compound of any one of embodiments 57 and 60-65, or a pharmaceutically acceptable salt thereof, wherein R.sup.a14 and R.sup.a15 are each independently hydrogen; C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, —OH, —O(C.sub.1-6 alkyl), —S(C.sub.1-6 alkyl), and halo; C.sub.2-6 alkenyl; C.sub.3-10 cycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of C.sub.2-6 alkenyl, C.sub.3-10 cycloalkyl, halo, cyano, —OH, —O(C.sub.1-6 alkyl), ═CR.sup.1a1R.sup.1a2, and C.sub.1-6 alkyl optionally substituted with one or more substituents independently selected from the group consisting of —OH, —O(C.sub.1-6 alkyl), and halo, wherein R.sup.1a1 and R.sup.1a2 are each independently hydrogen or C.sub.1-6 alkyl; C.sub.3-10 cycloalkenyl; or 3- to 12-membered heterocycloalkyl optionally substituted with one or more C.sub.1-6 alkyl.
67. The compound of any one of embodiments 57 and 60-66, or a pharmaceutically acceptable salt thereof, wherein R.sup.a14 is hydrogen and R.sup.a15 is tert-butyl.
68. The compound of any one of embodiments 57 and 60-67, or a pharmaceutically acceptable salt thereof, wherein ring A is substituted with one or more substituents independently selected from the group consisting of fluoro, chloro, —OH, methyl, amino,
##STR00596## ##STR00597## ##STR00598## ##STR00599## ##STR00600##
69. The compound of any one of embodiments 57 and 60-68, or a pharmaceutically acceptable salt thereof, wherein ring A is phenyl substituted with
##STR00601##
70. The compound of any one of embodiments 57 and 60-69, or a pharmaceutically acceptable salt thereof, wherein ring B is C.sub.5-7 cycloalkyl.
71. The compound ofany one of embodiments 57 and 60-69, or a pharmaceutically acceptable salt thereof, wherein ring B is 5- to 7-membered heterocycloalkyl.
72. The compound of any one of embodiments 57 and 60-69, or a pharmaceutically acceptable salt thereof, wherein ring B is
##STR00602##
wherein * denotes the point of attachment to the rest of Formula (I).
73. The compound of any one of embodiments 57 and 60-69, or a pharmaceutically acceptable salt thereof, wherein
##STR00603##
of Formula (I) is
[0297] ##STR00604##
wherein* denotes the point of attachment to the rest of Formula (I).
74. The compound of embodiment 73, or a pharmaceutically acceptable salt thereof, wherein
##STR00605##
of Formula (I) is
[0298] ##STR00606##
75. The compound of any one of embodiments 57 and 60-74, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
76. The compound of embodiment 75, or a pharmaceutically acceptable salt thereof, wherein R.sup.C1, R.sup.C3, and R.sup.C4 are each independently hydrogen, halo, or —NH.sub.2.
77. The compound of embodiment 75 or 76, or a pharmaceutically acceptable salt thereof, wherein R.sup.C1, R.sup.C3, and R.sup.C4 are each hydrogen.
78. The compound of any one of embodiments 57 and 60-74, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is N; Y.sup.2 is CR.sup.C2; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
79. The compound of any one of embodiments 57 and 60-74, or a pharmaceutically acceptable salt thereof, wherein Y.sup.1 is CR.sup.C1; Y.sup.2 is N; Y.sup.3 is CR.sup.C3; and Y.sup.4 is CR.sup.C4.
80. The compound of any one of embodiments 57 and 60-79, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is cyano, —OH, —CH.sub.2OH, bromo, —NO.sub.2,
##STR00607##
81. The compound of embodiment 80, or a pharmaceutically acceptable salt thereof, wherein R.sup.C2 is
##STR00608##
82. The compound of embodiment 57 or 60, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of compounds of Table 1.
83. The compound of embodiment 57, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of compounds of Table 2.
84. A pharmaceutical composition comprising a compound of any one of embodiments 57-83, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
85. A method of inhibiting KIF18A comprising contacting a cell with an effective amount of a compound of any one of embodiments 57-83, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 84.
86. A method of treating a disease or condition mediated by KIF18A in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of any one of embodiments 57-83, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 84.
87. A method of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of any one of embodiments 57-83, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition of embodiment 84.
88. The method of embodiment 87, wherein the cancer is selected from the group consisting of carcinomas, cancer of the anus, bladder, breast, colon, small intestine, appendix, kidney, renal pelvis, ureter, urothelium, liver, lung, pleura, esophagus, head and neck, nasopharynx, oropharynx, hypopharynx, oral cavity, larynx, biliary tract, gall-bladder, ovary, testicle, germ cell, uterus, pancreas, stomach, cervix, thyroid, prostate, salivary gland, or skin, hematopoietic tumors of lymphoid lineage, hematopoietic tumors of myeloid lineage, hematopoietic tumors of any lineage, myeloma, tumors of mesenchymal origin including sarcomas, tumors of the central and peripheral nervous system, tumor of neuroendocrine origin, tumor of endocrine origin, small cell tumors, tumors of unknown primary, other tumors comprising retinoblastoma, melanoma, seminoma, teratocarcinoma, osteosarcoma, and other cancer-related disorders that are a consequence of cancer presence or progression.
EXAMPLES
[0299] The following examples are offered to illustrate but not to limit the compositions, uses, and methods provided herein. The compounds are prepared using the general methods described above.
Abbreviations
[0300] BSA: bovine serum albumin [0301] DAST: diaminosulfur trifluoride [0302] dba: bibenzylidene acetone [0303] DMF: dimethylformamide [0304] EDCI: 1-ehthyl-3-(3-dimethylaminopropyl)carbodiimide [0305] ESI MS: electrospray mass spectrometry [0306] HATU: 1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate [0307] HOBT: 1-hydroxybenzotriazole [0308] HPLC: high-performance liquid chromatography [0309] IC.sub.50: 50% inhibitory concentration [0310] LDA: lithium diisopropylamide [0311] mCPBA: meta-chloroperoxybenzoic acid [0312] MsCl: methanesulfonyl chloride [0313] MTBE: methyl t-butyl ether [0314] NCS: N-chlorosuccinimide [0315] NCI: N-iodosuccinimide [0316] NMR: nuclear magnetic resonance [0317] PE: petroleum ether [0318] THF: tetrahydrofuran [0319] TFA: trifluoroacetic acid [0320] Xantphos: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene [0321] Xphos Pd G4: dicyclohexyl-[2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphanium; methanesulfonic acid; N-methyl-2-phenylaniline; palladium (CAS: 1599466-81-5)
Synthesis of Intermediates
Synthesis of 3-(piperidin-1-ylsulfonyl)benzoic acid (A-01)
[0322] ##STR00609##
[0323] Step 1. A mixture of piperidine (0.25 mL, 2.6 mmol), CH.sub.2Cl.sub.2 (5.0 mL), iPr.sub.2NEt (1.3 mL, 7.7 mmol) and methyl 3-chlorosulfonylbenzoate (900 mg, 3.84 mmol, 1.5 eq) was stirred for 2 h, concentrated, poured into H.sub.2O (20 mL), and extracted with EtOAc (2×10 mL). The extracts were combined, washed with brine (10.0 mL), dried over Na.sub.2SO.sub.4, filtered, and concentrated to provide methyl 3-(1-piperidylsulfonyl) benzoate (0.95 g).
[0324] Step 2. A mixture of methyl 3-(1-piperidylsulfonyl) benzoate (0.90 g, 3.2 mmol), THF (6.0 mL), H.sub.2O (2.0 mL), and LiOH.H.sub.2O (0.67 g, 16 mmol) was stirred for 2 h, then was concentrated. The mixture was treated with HCl (4N) to bring the pH to 3, poured into H.sub.2O (10 mL), and extracted with EtOAc (2×10 mL). The extracts were combined, washed with brine (10 mL), dried over Na.sub.2SO.sub.4, filtered, and concentrated to provide 3-(1-piperidylsulfonyl) benzoic acid (A-01, 0.72 g). ESI MS m/z: 270.0 (M+H).sup.+.
[0325] Compounds in Table 3 were prepared in the same manner as A-01 from the indicated sulfonyl chloride and amine.
TABLE-US-00003 TABLE 3 4 Structure Sulfonyl Chloride Amine A-02
Synthesis of 3-(cyclopentylsulfinyl)benzoic acid (A-51)
[0326] ##STR00826##
[0327] Step 1. A mixture of methyl 3-cyclopentylsulfanylbenzoate (0.50 g, 2.1 mmol), CH.sub.2Cl.sub.2 (25 mL), and MnO.sub.2 (0.37 g, 4.2 mmol) was stirred at 20° C. for 16 h. The mixture was extracted with EtOAc (100 mL×3), and the extracts were combined, dried over Na.sub.2SO.sub.4, filtered, and concentrated. The residue was purified silica gel chromatography (0-100% EtOAc/Petroleum ether) to provide methyl 3-cyclopentylsulfinylbenzoate (0.52 g).
[0328] Step 2. A mixture of methyl 3-cyclopentylsulfinylbenzoate (0.50 g, 2.0 mmol), THF (10 mL), H.sub.2O (10 mL), and LiOH (95 mg, 4.0 mmol) was stirred at 25° C. for 2 h, and then was concentrated. The pH was adjusted to pH 3 with 2M HCl and the mixture was extracted with EtOAc (50 mL×3). The combined extracts were dried over Na.sub.2SO.sub.4, filtered, and concentrated to provide 3-cyclopentylsulfinylbenzoic acid (A-51, 83 mg).
Synthesis of 3-(cyclopentylsulfonyl)benzoic acid (A-52)
[0329] ##STR00827##
[0330] Step 1. To a mixture of methyl 3-cyclopentylsulfanylbenzoate (0.50 g, 2.1 mmol) in HOAc (3.0 mL) was added H.sub.2O.sub.2 (30%, 1.2 mL, 13 mmol). The mixture was stirred at 80° C. for 12 h, H.sub.2O (20 mL) was added, and the mixture was extracted with EtOAc (10 mL×3). The extracts were combined, washed saturated Na.sub.2CO.sub.3 (20 mL×3), and aqueous of Na.sub.2SO.sub.3 (20 mL×3), and brine (30 mL). The extracts were dried over Na.sub.2SO.sub.4, filtered, and concentrated to provide methyl 3-cyclopentylsulfonylbenzoate (260 mg).
[0331] Step 2. A mixture of methyl 3-cyclopentylsulfonylbenzoate (0.28 g, 1.0 mmol), THF (5.0 mL), H.sub.2O (5 mL), and LiOH (50 mg, 2.1 mmol) was stirred at 25° C. for 2 h. The reaction mixture was extracted with MTBE (10 mL×2). The pH of the aqueous phase was adjusted to 3 with HCl and it was extracted with EtOAc (3×20 mL). The extracts were combined, washed with 20 mL of brine, dried over Na.sub.2SO.sub.4, filtered, and concentrated to provide 3-cyclopentylsulfonylbenzoic acid (0.29 g).
Synthesis of 3-(N-methylcyclopentanesulfonimidoyl)benzoic acid (A-53)
[0332] ##STR00828##
[0333] Step 1. To a mixture of methyl 3-cyclopentylsulfanylbenzoate (0.85 g, 3.6 mmol), EtOH (2 mL), and PhI(OAc).sub.2 (3.5 g, 11 mmol) was added NH.sub.4OAc (1.1 g, 14 mmol). The mixture was stirred at 20° C. for 2 h, concentrated, combined with H.sub.2O (30 mL), and extracted with EtOAc (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in petroleum ether) to provide methyl 3-(cyclopentylsulfonimidoyl) benzoate (0.50 g).
[0334] Step 2. To a 0° C. mixture of methyl 3-(cyclopentylsulfonimidoyl) benzoate (0.25 g, 0.94 mmol) and DMF (2 mL) was added NaH (60% in mineral oil, 45 mg, 1.1). The mixture was stirred at 0° C. for 0.5 h, and Mel (64 μL, 1.0 mmol) was added. The mixture was stirred at 20° C. for 12 h, poured into H.sub.2O (30 mL) and extracted with EtOAc (2×30 mL). The extracts were combined, washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated to provide 3-(S-cyclopentyl-N-methyl-sulfonimidoyl)benzoic acid (A-53, 0.25 g).
Synthesis of 3-(cyclopentanecarbonyl)benzoic acid (A-54)
[0335] ##STR00829##
[0336] Step 1. To a −50° C. mixture of methyl 3-cyanobenzoate (1.0 g, 6.2 mmol), CuI (0.37 g, 1.9 mmol), and THF (30 mL) was slowly added cyclopentylmagnesium bromide (1 M in THF, 24 mL, 24 mmol). The mixture was stirred at −50° C. for 5 h, then at 20° C. for 1 h, and saturated aqueous NH.sub.4Cl (10 mL) was added at 0° C. EtOAc (20 mL) was added, and the layers separated. The aqueous wash was extracted with EtOAc (10 mL), and extracts were combined, washed with brine (15 mL×2), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (0-20% EtOAc/petroleum ether) to provide methyl 3-(cyclopentanecarbonyl) benzoate (0.22 g).
[0337] Step 2. A degassed mixture of methyl 3-(cyclopentanecarbonyl) benzoate (0.22 g, 0.95 mmol), LiOH (0.11 g, 4.7 mmol), THF (0.9 mL), H.sub.2O (0.3 mL) was stirred at 25° C. for 4 h. The mixture was concentrated, combined with H.sub.2O (10 mL), and extracted with MTBE (2 mL). The pH of the aqueous phase was adjusted to between 2 and 3 with 2N HCl. The resulting precipitate was filtered and dried under vacuum to provide 3-(cyclopentanecarbonyl)benzoic acid (A-54, 120 mg).
Synthesis of 3-(cyclobutanecarbonyl)benzoic acid (A-77)
[0338] ##STR00830##
[0339] 3-(Cyclobutanecarbonyl)benzoic acid was prepared from methyl 3-cyanobenzoate and cyclobutanemagnesium bromide in the same manner as A-54.
Synthesis of 3-(2-cyclobutylacetyl)benzoic acid (A-75)
[0340] ##STR00831##
[0341] Step 1. To a mixture of 3-bromobenzonitrile (2.0 g, 11 mmol) and THF (10 mL) at −50° C. was added CuI (2.1 g, 11 mmol) and bromo(cyclobutylmethyl)magnesium (1 M, 13.2 mL). The mixture was stirred at −50° C. for 5 h then at 20° C. for 1 h. The mixture was poured into H.sub.2O (20 mL) and extracted with EtOAc (2×20 mL). The combined extracts were washed with brine (20 mL), dried over Na.sub.2sO.sub.4, concentrated, purified by silica chromatography (0-20% EtOAC in PE) to provide 1-(3-bromophenyl)-2-cyclobutylethan-1-one (1.3 g).
[0342] Step 2. A mixture of 1-(3-bromophenyl)-2-cyclobutylethan-1-one (1.1 g, 4.4 mmol), MeOH (4 mL), DMF (16 mL), Et.sub.3N (1.8 mL, 13 mmol), 3-diphenylphosphanylpropyl-(diphenyl)phosphane (0.36 g, 0.87 mmol), and Pd(OAc).sub.2 (0.20 g, 0.87 mmol) was stirred at 90° C. for 12 h under CO (50 psi). The mixture was poured to water (30 mL), extracted with EtOAc (2×30 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-20% EtOAc in PE) provide methyl 3-(2-cyclobutylacetyl)benzoate (0.80 g).
[0343] Step 3. A mixture of methyl 3-(2-cyclobutylacetyl)benzoate (0.50 g, 2.2 mmol), THF (0.6 mL), H.sub.2O (0.2 mL), and LiOH (0.16 g, 6.7 mmol) was stirred at 20° C. for 2 h. The mixture was concentrated to remove THF, and HCl (0.5 M, 5 mL) was added. The mixture was extracted with EtOAc (2×30 mL) and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 3-(2-cyclobutylacetyl)benzoic acid (0.36 g, 46% purity).
Synthesis of 3-(cyclopentyldifluoromethyl)benzoate (A-76)
[0344] ##STR00832##
[0345] Step 1. To a mixture of methyl 3-(cyclopentanecarbonyl)benzoate (0.16 mg, 0.69 mmol) and CH.sub.2Cl.sub.2 (1 mL) was added BF.sub.3.Et.sub.2O (0.64 mL, 5.2 mmol) and ethane-1,2-dithiol (0.10 mL, 1.2 mmol). The mixture was stirred at 20° C. for 18 h, poured into water (20 mL), and extracted with CH.sub.2Cl.sub.2 (2×30 mL). The combined extracts were washed with brine (10 mL), dried Na.sub.2SO.sub.4, concentrated, purified by preparative TLC (10% EtOAc/PE) to provide methyl 3-(2-cyclopentyl-1,3-dithiolan-2-yl)benzoate (0.20 g).
[0346] Step 2. To a mixture of methyl 3-(2-cyclopentyl-1,3-dithiolan-2-yl)benzoate (0.20 g, 0.65 mmol) and CH.sub.2Cl.sub.2 (10 mL) was added NIS (0.29 g, 1.3 mmol) and pyridine hydrofluoride (0.33 mL, 2.6 mmol) at −70° C. The mixture was stirred at −70° C. for 0.5 h, poured into H.sub.2O (10 mL) and extracted with EtOAc (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative TLC (10% EtOAc in PE) to provide methyl 3-[cyclopentyl(difluoro)methyl]benzoate (80 mg).
[0347] Step 3. A mixture of methyl 3-[cyclopentyl(difluoro)methyl]benzoate (80 mg, 0.32 mmol), THF (3 mL), H.sub.2O (1 mL), and LiOH (23 mg, 0.94 mmol) was stirred at 20° C. for 2 h. The mixture was concentrated, combined with HCl (0.5 M, 5 mL), and extracted with EtOAc (2×30 mL). The combined extract was washed with brine (10 mL), dried Na.sub.2SO.sub.4, concentrated, to provide 3-[cyclopentyl(difluoro)methyl]benzoic acid (A-76, 91 mg).
Synthesis of 3-(cyclopentanesulfonimidoyl)benzoic acid (A-72)
[0348] ##STR00833##
[0349] A mixture of methyl 3-(cyclopentylsulfonimidoyl)benzoate (0.80 g, 3.0 mmol), THF (18 mL), H.sub.2O (6 mL), and LiOH.H.sub.2O (0.38 g, 9.0 mmol) was stirred at 25° C. for 12 h, then was poured into water (20 mL) and =extracted with EtOAc (2×10 mL). The organic phase was washed with brine (20 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 3-(cyclopentanesulfonimidoyl)benzoic acid (A-72, 0.3 g). .sup.1H NMR (DMSO-d.sup.6, 400 MHz) δ ppm 13.72-13.06 (m, 1H), 8.40-8.38 (s, 1H), 8.20-8.17 (m, 1H), 8.13-8.09 (m, 1H), 7.76-7.72 (m, 1H), 3.68-3.60 (m, 1H), 1.91-1.70 (m, 4H), 1.62-1.47 (m, 4H).
Synthesis of 2-(cyclopentyl(hydroxy)methyl)isonicotinic acid (A-78)
[0350] ##STR00834##
[0351] Step 1. To a −60° C. mixture of methyl 2-formylisonicotinate (1.0 g, 6.0 mmol) and THF (25 mL) was added cyclopentylmagnesium bromide (1 M, 7.3 mL) over 15 min. The resulting mixture was stirred at −60° C. for 1.75 h, poured into water (50 mL), and extracted with EtOAc (2×50 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide methyl 2-(cyclopentyl(hydroxy)methyl)isonicotinate (0.20 g).
[0352] Step 2. A mixture of methyl 2-(cyclopentyl(hydroxy)methyl)isonicotinate (0.18 g, 0.77 mmol), THF (2 mL), and H.sub.2O (1 mL), and LiOH.H.sub.2O (96 mg, 2.0 mmol) was stirred at 25° C. for 2 h, poured into water (30 mL), and extracted with MTBE (2×20 mL). The aqueous layer was collected, and the pH was adjusted to 5 by the careful addition of 2N HCl. The mixture was concentrated to provide 2-(cyclopentyl(hydroxy)methyl)isonicotinic acid (A-78).
Synthesis of 3-((3,3-difluorocyclobutyl)sulfonyl)benzoic acid (A-82)
[0353] ##STR00835##
[0354] Step 1. To mixture of 3-bromobenzenethiol (3.4 mL, 33 mmol), 4-bromobut-1-ene (4.4 mL, 43 mmol), DMF (50 mL), and K.sub.2CO.sub.3 (6.8 g, 49 mmol) was stirred at 60° C. for 4 h, combined with 1M aq. Na.sub.2S.sub.2O.sub.3 and saturated aqueous NaHCO.sub.3 (30 mL), and extracted with CH.sub.2Cl.sub.2 (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide 1-bromo-3-but-3-enylsulfanyl-benzene (6.50 g).
[0355] Step 2. To a mixture of 1-bromo-3-but-3-enylsulfanyl-benzene (6.5 g, 27 mmol) and CH.sub.2Cl.sub.2 (50 mL) was added mCPBA (27 g, 0.13 mol, 85% purity). The mixture was stirred at 20° C. for 12 h, combined with 1M aqueous Na.sub.2S.sub.2O.sub.3 and saturated aqueous NaHCO.sub.3 (30 mL), extracted with CH.sub.2Cl.sub.2 (2×30 mL), washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide 2-[2-(3-bromophenyl)sulfonylethyl]oxirane (5.1 g).
[0356] Step 3. To a mixture of 2-[2-(3-bromophenyl)sulfonylethyl]oxirane (5.1 g, 18 mmol) and THF (50 mL) was added MeMgBr (3 M, 23 mL, 69 mmol) at −70° C. The mixture was stirred at 20° C. for 12 h, poured into saturated aqueous NH.sub.4Cl (20 mL), and extracted with EtOAc (2×20 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide 3-(3-bromophenyl)sulfonylcyclobutanol (4.3 g).
[0357] Step 4. To a mixture of 3-(3-bromophenyl)sulfonylcyclobutanol (1.00 g, 3.4 mmol), H.sub.2O (10 mL), MeCN (5 mL), and CH.sub.2Cl.sub.2 (5 mL) at 40° C. were added RuCl.sub.3.H.sub.2O (8 mg, 34 μmol) and NaIO.sub.4 (3.7 g, 17 mmol). The mixture was stirred at 40° C. for 12 h, cold water (30 mL) was added, and the mixture was extracted with CH.sub.2Cl.sub.2 (2×30 mL). The combined extracts were washed with saturated aqueous NaHCO.sub.3 and brine, dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide 3-(3-bromophenyl)sulfonylcyclobutanone (0.64 g).
[0358] Step 5. To a mixture of 3-(3-bromophenyl)sulfonylcyclobutanone (0.64 g, 2.2 mmol) and CH.sub.2Cl.sub.2 (6 mL) was added DAST (0.88 mL, 6.6 mmol) over 0.5 h at −70° C. The mixture was stirred for 1 h, and then allowed to warm 20° C. and stirred for 16 h. The mixture was poured into saturated aqueous NaHCO.sub.3 (10 mL) and the extracted with CH.sub.2Cl.sub.2 (2×10 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide 1-bromo-3-(3,3-difluorocyclobutyl)sulfonyl-benzene (0.60 g).
[0359] Step 6. CO gas was bubbled through a stirring mixture of 1-bromo-3-(3,3-difluorocyclobutyl)sulfonyl-benzene (0.55 g, 1.8 mmol), Et.sub.3N (0.49 mL, 3.5 mmol), DMF (6 mL), MeOH (3 mL), bis(diphenylphosphino)propane (73 mg, 0.18 mmol), and Pd(OAc).sub.2 (40 mg, 0.18 mmol) for 5 mins and the mixture was then heated at 80° C. under a CO atmosphere at 15 psi for 12 h. The mixture was poured into water (30 mL), extracted with EtOAc (2×30 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide methyl 3-(3,3-difluorocyclobutyl)sulfonylbenzoate (0.44 g).
[0360] Step 7. A mixture of methyl 3-(3,3-difluorocyclobutyl) sulfonylbenzoate (0.44 g, 1.5 mmol), THF (5 mL), H.sub.2O (1.5 mL), and LiOH.H.sub.2O (0.25 g, 6.1 mmol) was stirred at 40° C. for 2 h, concentrated, combined with H.sub.2O (30 mL), 2N HCl was added until the pH was between 3 and 4, and the resulting mixture was extracted with EtOAc (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 3-((3,3-difluorocyclobutyl)sulfonyl)benzoic acid (A-82, 0.33 g).
Synthesis of 5-(cyclopentylsulfonyl)thiophene-3-carboxylic acid (A-83)
[0361] ##STR00836##
[0362] Step 1. A mixture of methyl 5-bromothiophene-3-carboxylate (1.0 g, 4.5 mmol), 1,4-dioxane (25 mL), iPr.sub.2NEt (2.0 mL, 11 mmol), Pd.sub.2(dba).sub.3 (0.41 g, 0.45 mmol), cyclopentanethiol (0.73 mL, 6.8 mmol), and Xantphos (0.26 g, 0.45 mmol) was stirred at 110° C. for 12 h. The mixture was poured into H.sub.2O (20 mL), extracted with EtOAc (2×10 mL), and the combined extracts were washed with brine (20 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-50% EtOAc in PE) to provide methyl 5-cyclopentylsulfanylthiophene-3-carboxylate (1.0 g).
[0363] Step 2. To a mixture of methyl 5-cyclopentylsulfanylthiophene-3-carboxylate (0.70 g, 2.9 mmol) and CH.sub.2Cl.sub.2 (20 mL) was added mCPBA (2.4 g, 12 mmol, 85% purity). The mixture was stirred at 20° C. for 12 h, poured into saturated Na.sub.2SO.sub.3 (10 mL), and extracted with EtOAc (2×5 mL). The combined extracts were washed with brine (10 mL), dried over anhydrous Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-50% EtOAc in PE) to provide methyl 5-cyclopentylsulfonylthiophene-3-carboxylate (0.70 g).
[0364] Step 3. A mixture methyl 5-cyclopentylsulfonylthiophene-3-carboxylate (0.71 g, 2.6 mmol), THF (9 mL), H.sub.2O (3 mL), and LiOH.H.sub.2O (0.32 g, 7.7 mmol) was stirred at 20° C. for 12 h, poured into H.sub.2O (10 mL), and the pH was adjusted to 3-4 with HCl (2 N). The resulting mixture was extracted with EtOAc (2×5 mL). The extracts were combined, washed with brine (5 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-50% EtOAc in PE) to provide 5-(cyclopentylsulfonyl)thiophene-3-carboxylic acid (A-83, 0.40 g).
Synthesis of 3-(cyano(cyclopentyl)methyl)benzoic acid (A-85)
[0365] ##STR00837##
[0366] Step 1. To a mixture of methyl 3-(cyanomethyl)benzoate (0.10 g, 0.58 mmol) and DMF (2 mL) was added NaH (27 mg, 0.69 mmol, 285 uL, 60% purity, 1.2 eq) at 0° C. After stirring for 0.5 h, bromocyclopentane (0.12 mL, 1.1 mmol) was added dropwise at 0° C. The resulting mixture was stirred at 25° C. for 2 h, and saturated aqueous NH.sub.4Cl (2 mL) and H.sub.2O (10 mL) were added at 0° C. The mixture was extracted with EtOAc (10 mL×3), and the combined extracts were washed with brine (10 mL×3), dried over Na.sub.2SO.sub.4, filtered, concentrated, purified by silica chromatography (0-15% EtOAc in PE) to provide methyl 3-(cyano(cyclopentyl)methyl)benzoate (0.10 g).
[0367] Step 2. A mixture of methyl 3-(cyano(cyclopentyl)methyl)benzoate (0.10 g, 0.41 mmol), THF (3 mL), H.sub.2O (3 mL), and LiOH.H.sub.2O (35 mg, 0.82 mmol) was stirred at 20° C. for 4 h, concentrated, and the pH adjusted to 4 by the dropwise addition of 2M HCl. The mixture was extracted with EtOAc (20 mL×3), and the combined extracts were dried over Na.sub.2SO.sub.4, filtered, and concentrated to provide 3-(cyano(cyclopentyl)methyl)benzoic acid (A-85, 0.11 g).
Synthesis of 3-(1-(4,4-difluoropiperidin-1-yl)ethyl)benzoic acid (A-86)
[0368] ##STR00838##
[0369] Step 1. A mixture of methyl 3-acetylbenzoate (1.0 g, 5.6 mmol) and 4,4-difluoropiperidine hydrochloride (0.88 g, 5.6 mmol), 1,2-dichloroethane (20 mL), Ti(OiPr).sub.4 (6.6 mL, 23 mmol) and then was stirred at 80° C. for 12 h. NaBH(OAc).sub.3 (3.6 g, 17 mmol) was added and the mixture was stirred at 80° C. for 2 h, poured into water (20 mL), and extracted with EtOAc (2×20 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide isopropyl 3-[1-(4,4-difluoro-1-piperidyl)ethyl]benzoate (1.5 g).
[0370] Step 2. A mixture of isopropyl 3-[1-(4,4-difluoro-1-piperidyl)ethyl]benzoate (1.4 g, 4.6 mmol) in THF (14 mL), MeOH (3.3 mL), and H.sub.2O (3.3 mL), and LiOH (0.33 g, 14 mmol) was stirred at 25° C. for 2 h. The mixture was concentrated, combined with H.sub.2O (28 mL) and washed with EtOAc (2×28 mL). The aqueous solution was treated with 2M HCl until a pH of 2, and the resulting mixture was concentrated to provide 3-[1-(4,4-difluoro-1-piperidyl)ethyl]benzoic acid (A-86, 0.91 g).
Synthesis of 6-((4,4-difluoropiperidin-1-yl)methyl)picolinic acid (A-87)
[0371] ##STR00839##
[0372] Step 1. A mixture of methyl 6-formylpyridine-2-carboxylate (0.50 g, 3.0 mmol) and 4,4-difluoropiperidine (477 mg, 3.0 mmol, 1.0 eq, HCl) in MeOH (10 mL) was added HOAc (545 mg, 9.1 mmol, 519 uL, 3.0 eq), NaOAc (745 mg, 9.1 mmol, 3.0 eq) and then was stirred at 25° C. for 1 hour. Then added NaBH.sub.3CN (761 mg, 12.1 mmol, 4.0 eq), the mixture was stirred at 25° C. for 1 hour. The reaction was poured into water (10 mL) and the resulting mixture was extracted with EtOAc (2×10 mL). The organic phase was washed with brine (10 mL), dried over anhydrous Na.sub.2SO.sub.4, concentrated in vacuum to afford the compound methyl 6-[(4,4-difluoro-1-piperidyl)methyl]pyridine-2-carboxylate (500 mg, crude) as a yellow solid.
Synthesis of 3-((3,3-difluoropyrrolidin-1-yl)methyl)benzoic acid (A-92)
[0373] ##STR00840##
[0374] 3-((3,3-difluoropyrrolidin-1-yl)methyl)benzoic acid (A-92) was prepared from methyl 3-formylbenzoate in the mannet described for the synthesis of A-87.
Synthesis of 2-((4,4-difluoropiperidin-1-yl)methyl)-6-methylpyrimidine-4-carboxylic acid (A-88)
[0375] ##STR00841##
[0376] A mixture of potassium ((4,4-difluoropiperidin-1-yl)methyl)trifluoroborate (CAS: 1708960-44-4, 1.1 g, 4.6 mmol), methyl 2-chloro-6-methyl-pyrimidine-4-carboxylate (0.28 g, 1.5 mmol), H.sub.2O (2 mL), THF (8 mL) Cs.sub.2CO.sub.3 (1.5 g, 4.6 mmol), and Xphos Pd G4 (65 mg, 76 μmol). The mixture was stirred at 80° C. for 12 h, diluted with water (10 mL), and extracted with EtOAc (10 mL×3). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by preparative HPLC (C18, 1-10% MeCN in H.sub.2O [formic acid]) to provide 2-((4,4-difluoropiperidin-1-yl)methyl)-6-methylpyrimidine-4-carboxylic acid (A-88, 50 mg).
Synthesis of 3-(isoxazolidin-2-ylmethyl)benzoic acid (A-89)
[0377] ##STR00842##
[0378] Step 1. A mixture of methyl 3-(bromomethyl)benzoate (0.30 g, 1.3 mmol), DMF (3 mL), isoxazolidine hydrochloride (0.14 g, 1.3), and iPr.sub.2NEt (0.68 mL, 3.9 mmol) was stirred at 60° C. for 12 h. The mixture was combined with 0° C. H.sub.2O (10 mL) and extracted with EtOAc (10 mL×2). The combined extracts were washed with H.sub.2O (10 mL) and brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide methyl 3-(isoxazolidin-2-ylmethyl)benzoate (0.17 g).
[0379] Step 2. A mixture of methyl 3-(isoxazolidin-3-ylmethyl)benzoate (0.17 g, 0.77 mmol), 1,4-dioxane (1.5 mL), H.sub.2O (0.5 mL) and LiOH.H.sub.2O (32 mg, 0.77 mmol) was stirred at 20° C. for 12 h, and H.sub.2O (5 mL) and MTBE (10 mL). The aqueous phase was collected and the pH adjusted to 6.0 by addition of HCl (2 N). The aqueous phase was concentrated to provide 3-(isoxazolidin-3-ylmethyl)benzoic acid (A-89, 0.17 g, crude).
Synthesis of 3-((6,6-difluoro-3-azabicyclo[3.1.0]hexan-3-yl)methyl)benzoic acid (A-96)
[0380] ##STR00843##
[0381] Synthesis of 3-((6,6-difluoro-3-azabicyclo[3.1.0]hexan-3-yl)methyl)benzoic acid (A-96) was prepared in the same manner as A-89 by substituting 6,6-difluoro-3-azabicyclo[3.1.0]hexane hydrochloride for isoxazolidine hydrochloride Synthesis of 3-(cyclopentylamino)benzoic acid (A-90)
##STR00844##
[0382] Step 1. A mixture of methyl 3-aminobenzoate (1.0 g, 6.6 mmol). cyclopentanone (2.9 mL, 33 mmol), MeOH (10 mL), and HOAc (0.38 mL, 6.6 mmol) was stirred for 3 hours, and NaBH.sub.3CN (0.62 g, 9.9 mmol) was added in portions. The resulting mixture was stirred for 11 h, poured into water (50 mL), and extracted with EtOAc (2×25 mL). The extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-50% EtOAc in PE) to provide methyl 3-(cyclopentylamino)benzoate (1.33 g, 91.68% yield) as a white solid.
[0383] Step 2. A mixture of methyl 3-(cyclopentylamino)benzoate (0.10 g, 0.46 mmol), THF (0.9 mL), H.sub.2O (0.3 mL), and LiOH.H.sub.2O (96 mg, 2.3 mmol) was stirred at 60° C. for 6 h, poured into H.sub.2O (10 mL), and the pH adjusted to 5-6 with HCl (2 N). The resulting mixture was extracted with EtOAc (2×5 mL), the extracts were washed with brine (5 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 3-(cyclopentylamino)benzoic acid (A-90, 53 mg).
Synthesis of 3-(cyclopentyl(methyl)amino)benzoic acid (A-91)
[0384] ##STR00845##
[0385] Step 1. To a mixture of methyl 3-(cyclopentylamino)benzoate (0.50 g, 2.0 mmol), paraformaldehyde (0.41 mg, 5 mmol), and dichloroethane (5 mL) was added HOAc (0.16 mL, 3.0 mmol) dropwise at 20° C. After stirring for 1 h, and NaBH(OAc).sub.3 (0.97 g, 5 mmol) and the mixture was stirred at 60° C. for 11 h. The reaction was poured into water (20 mL) and the resulting mixture was extracted with EtOAc (2×15 mL). The organic phase was washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-50% EtOAc in PE) to provide methyl 3-[cyclopentyl(methyl)amino]benzoate (0.42 g).
[0386] Step 2. A mixture of methyl 3-[cyclopentyl(methyl)amino]benzoate (0.23 g, 0.98 mmol), THF (3 mL), and H.sub.2O (1 mL), and LiOH.H.sub.2O (0.12 g, 3.0 mmol) was stirred at 60° C. for 2 h. The mixture was poured into water (10 mL), the pH adjusted to 3-4 with HCl (2 N), and was extracted with EtOAc (2×5 mL). The extracts were washed with brine (5 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 3-(cyclopentyl(methyl)amino)benzoic acid (A-91, 0.30 g).
Synthesis of 3-(3,3-difluorocyclobutane-1-carbonyl)benzoic acid (A-93)
[0387] ##STR00846##
[0388] Step 1. To a −70° C. mixture of 1-bromo-3-iodo-benzene (1.3 mL, 10 mmol) and THF (20 mL), was added dropwise BuLi (1 M, 10 mL). The mixture was stirred for 30 min. and 3,3-difluoro-N-methoxy-N-methyl-cyclobutanecarboxamide (1.5 g, 8.4 mmol) in THF (10 mL) was added dropwise at −70° C. The resulting mixture was stirred at 20° C. for 1.5 h, poured into saturated aqueous NH.sub.4Cl (10 mL), and extracted with EtOAc (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-100% EtOAc in PE) to provide (3-bromophenyl)-(3,3-difluorocyclobutyl) methanone (1.1 g).
[0389] Step 2. A mixture of (3-bromophenyl)-(3,3-difluorocyclobutyl)methanone (1.0 g, 3.6 mmol), MeOH (5 mL), DMF (10 mL), Et.sub.3N (1.5 mL, 11 mmol), 3-diphenylphosphanylpropyl (diphenyl)phosphane (0.30 g, 0.73 mmol), Pd(OAc).sub.2 (0.16 g, 0.73 mmol) was stirred at 80° C. for 12 h under CO (50 psi). The mixture was concentrated, poured into H.sub.2O (10 mL), and extracted with EtOAc (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative TLC (10% EtOAc in PE) to provide methyl 3-(3,3-difluorocyclobutanecarbonyl)benzoate (0.80 g).
[0390] Step 3. A mixture methyl 3-(3,3-difluorocyclobutanecarbonyl)benzoate (0.80 g, 3.2 mmol), THF (0.6 mL), H.sub.2O (0.2 mL), and LiOH.H.sub.2O (226 mg, 9.4 mmol, 3.0 eq) The mixture was stirred at 20° C. for 2 h, concentrated, and HCl (0.5 M, 5 mL) was added. The mixture was extracted with EtOAc (10 mL), and the extract was concentrated to provide 3-(3,3-difluorocyclobutane-1-carbonyl)benzoic acid (A-93, 0.50 g).
Synthesis of 3-(1-methylcyclobutane-1-carbonyl)benzoic acid (A-94)
[0391] ##STR00847##
[0392] 3-(1-methylcyclobutane-1-carbonyl)benzoic acid (A-94) was prepared in the same manner as A-93.
Synthesis of 4-(cyclopentanecarbonyl)thiophene-2-carboxylic acid (A-98)
[0393] ##STR00848##
[0394] nBuLi (2.5 M, 3.9 mL, 2.5 eq) was added dropwise to 4-bromothiophene-2-carboxylic acid (0.80 g, 3.9 mmol) in THF (15 mL) over 5 min at −78° C. The mixture was stirred for 25 min, and N-methoxy-N-methyl-cyclopentanecarboxamide (0.91 g, 5.8 mmol) was added at −78° C. The resulting mixture was stirred at 20° C. for 12 h, combined with saturated NH.sub.4Cl 1 mL at −78° C. and H.sub.2O (5 mL) and extracted with EtOAc (10 mL×3). The combined extracts were washed with brine (10 mL), dried Na.sub.2SO.sub.4, filtered, concentrated, and purified by preparative HPLC (C18, 20-50% MeCN in H.sub.2O [HCl]) to provide 4-(cyclopentanecarbonyl) thiophene-2-carboxylic acid (A-98, 10%).
Synthesis of 5-(cyclopentyl(hydroxy)methyl)furan-2-carboxylic acid (A-99)
[0395] ##STR00849##
[0396] To a mixture of furan-2-carboxylic acid (2.0 g, 18 mmol) and THF (20 mL) was added dropwise LDA (2 M, 13 mL) at −70° C. The mixture was stirred 0.5 h, and cyclopentanecarbaldehyde (2.6 g, 27 mmol) in THF (20 mL) was added dropwise at −70° C. The resulting mixture was stirred at 20° C. for 1.5 h, poured into saturated NH.sub.4Cl (10 mL), and the extracted with EtOAc (2×10 mL). The aqueous phase purified by preparative HPLC (0.1% FA condition) to provide 5-(cyclopentyl(hydroxy)methyl)furan-2-carboxylic acid (A-99, 0.38 g).
[0397] Compounds in Table 3.1 were prepared from furan-2-carboxylic acid and the indicated aldehyde in the manner described for the synthesis of A-99
TABLE-US-00004 TABLE 3.1 Code Compound Aldehyde A-100
Synthesis of 3-(N-(3,3-difluorocyclobutyl)-N-methylsulfamoyl)benzoic acid (A-95)
[0398] ##STR00853##
[0399] Step 1. To two mixtures of methyl 3-[(3,3-difluorocyclobutyl)sulfamoyl]benzoate (intermediate from synthesis of A-36, 0.30 & 0.10 g, 0.98 & 0.33 mmol) and DMF (4.0 & 1.3 mL) was added NaH (59 & 20 mg, 1.5 & 0.5 mmol, 60% purity) at 0° C. The mixtures were stirred for 30 min, Mel (73 & 24 μL, 1.2 & 0.4 mmol) was added, and the mixtures were stirred at 20° C. for 30 min. The mixtures were combined and poured into water (10 mL), extracted with EtOAc (10 mL×2), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (10-100% EtOAc in PE) to provide methyl 3-[(3,3-difluorocyclobutyl)-methyl-sulfamoyl]benzoate (0.28 g).
[0400] Step 2. Two mixtures of methyl 3-[(3,3-difluorocyclobutyl)-methyl-sulfamoyl]benzoate (0.23 & 0.050 g, 0.72 & 0.16 mmol), THF (1.8 & 0.4 mL), H.sub.2O (0.6 & 0.13 mL) was added LiOH.H.sub.2O (91 & 20 mg, 2.2 & 0.48 mmol) were stirred at 20° C. for 4 h. The mixtures were combined, partially concentrated, and the pH adjusted to 3 by the addition of 2N HCl. The mixture was extracted with EtOAc (2×10 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 3-(N-(3,3-difluorocyclobutyl)-N-methylsulfamoyl)benzoic acid (A-95, 0.29 g).
Synthesis of 3-((cyclobutylmethyl)(methyl)phosphoryl)benzoic acid (A-97)
[0401] ##STR00854##
[0402] Step 1. To a mixture of 1-bromo-3-ethoxyphosphonoyl-benzene (1.8 g, 7.2 mmol) and DMF (20 mL) was added NaH (0.87 g, 22 mmol, 60% purity) at 0° C. The mixture was stirred for 30 min and iodomethylcyclobutane (1.6 mL, 14 mmol) was added. The mixture was stirred at 0-20° C. for 60 min, poured into saturated NH.sub.4Cl (20 mL), and extracted with EtOAc (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-50% EtOAc in PE) to provide 1-bromo-3-[cyclobutylmethyl(ethoxy)phosphoryl]benzene (0.85 g).
[0403] Step 2. To a 0° C. mixture of 1-bromo-3-[cyclobutylmethyl(ethoxy)phosphoryl]benzene (0.68 g, 2.1 mmol) and THF (6 mL) was added MeMgBr (3 M, 6.4 mL) was stirred at 20° C. for 4 h, poured into saturated NH.sub.4Cl (20 mL), and extracted with EtOAc (2×15 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-50% EtOAc in PE) to provide 1-bromo-3-[cyclobutylmethyl(methyl)phosphoryl]benzene (0.56 g).
[0404] Step 3. A mixture of 1-bromo-3-[cyclobutylmethyl(methyl)phosphoryl]benzene (0.49 g, 1.7 mmol), MeOH (4 mL), 1,4-dioxane (4 mL), Mo(CO).sub.6 (0.11 g, 0.43 mmol), K.sub.3PO.sub.4 (0.36 g, 1.7 mmol), DMAP (0.10 g, 0.85 mmol), Xantphos (99 mg, 0.17 mmol), and Pd(OAc).sub.2 (19 mg, 85 μmol) was stirred at 120° C. for 3 h. The reaction was poured into water (20 mL) and the resulting mixture was extracted with EtOAc (2×15 mL). The organic phase was washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-10% MeOH in CH.sub.2Cl.sub.2) to provide methyl 3-[cyclobutylmethyl(methyl)phosphoryl]benzoate (0.34 g).
[0405] Step 4. A mixture of methyl 3-[cyclobutylmethyl(methyl)phosphoryl]benzoate (0.32 g, 1.2 mmol), THF (3 mL), H.sub.2O (1 mL), and LiOH.H.sub.2O (0.15 g, 3.6 mmol) was stirred for 12 h, poured into H.sub.2O (10 mL), and HCl (2 N) added to adjust the pH to 3-4, and extracted with EtOAc (2×5 mL). The combined extracts were washed with brine (5 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 3-((cyclobutylmethyl)(methyl)phosphoryl)benzoic acid (A-97, 0.17 g).
[0406] Synthesis of 4-(difluoromethyl)cyclohexane-1-carbaldehyde
##STR00855##
[0407] Step 1. To a 0° C. mixture of methyl 4-formylcyclohexanecarboxylate (5.0 g, 29 mmol) and CH.sub.2Cl.sub.2 (50 mL) was added slowly DAST (12 mL, 88 mmol). The mixture was stirred at 20° C. for 12 h, poured into saturated aqueous of NaHCO.sub.3 (30 mL), and extracted with CH.sub.2Cl.sub.2 (2×80 mL). The combined extracts were washed with brine (30 mL), dried over Na.sub.2SO.sub.4, concentrated, purified by silica chromatography (5-17% EtOAc in petroleum ether) to provide methyl 4-(difluoromethyl)cyclohexanecarboxylate (3.2 g).
[0408] Step 2. A solution of 4-(difluoromethyl)cyclohexanecarboxylate (3.2 g, 17 mmol) in THF (10 mL) was slowly added to LiAlH.sub.4 (1.3 g, 33 mmol) in THF (20 mL) and then stirred at 25° C. for 2 h. H.sub.2O (1.3 mL), aqueous NaOH (85%, 1.3 mL), and additional H.sub.2O (1.3 mL) were added and the mixture was filtered. The filtrate was concentration to provide [4-(difluoromethyl) cyclohexyl] methanol (1.80 g).
[0409] Step 3. To a mixture of [4-(difluoromethyl)cyclohexyl]methanol (1.6 g, 9.7 mmol), NaHCO.sub.3 (6.6 g, 78 mmol), and CH.sub.2Cl.sub.2 (50 mL) was added Dess-Martin periodinane (8.3 g, 20 mmol). The mixture was stirred at 25° C. for 2, then was poured into a mixture of saturated aqueous of NaHCO.sub.3 (15 mL) and saturated aqueous of Na.sub.2SO.sub.3 (15 mL). The resulting mixture was filtered and extracted with CH.sub.2Cl.sub.2 (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (5-17% EtOAc in petroleum ether) to provide 4-(difluoromethyl)cyclohexanecarbaldehyde (1.4 g).
Synthesis of 4-fluoro-4-methylcyclohexane-1-carbaldehyde
[0410] ##STR00856##
[0411] Step 1. To a mixture of ethyl 4-oxocyclohexanecarboxylate (4.7 mL, 29 mmol) in THF (30 mL) was slowly added MeLi (1 M, 41 mL) at −60° C. The mixture was stirred at −60° C. for 1 h, poured into NH.sub.4Cl (20 mL), and extracted with EtOAc (2×20 mL). The combined extracts were washed with brine (20 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (13-50% EtOAc in PE) to ethyl 4-hydroxy-4-methyl-cyclohexanecarboxylate (2.20 g).
[0412] Step 2. To a solution of ethyl 4-hydroxy-4-methyl-cyclohexanecarboxylate (2.4 g, 13 mmol) and CH.sub.2Cl.sub.2 (1 mL) was added DAST (1.7 mL, 13 mmol). The mixture was stirred at −40° C. for 1 h, poured into 1M Na.sub.2HCO.sub.3 (20 mL), and extracted with EtOAc (2×20 mL). The combined extracts were washed with brine (15 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (15-50% EtOAc in PE) to provide ethyl 4-fluoro-4-methyl-cyclohexanecarboxylate (1.60 g).
[0413] Step 3. To a 0° C. mixture of ethyl 4-fluoro-4-methyl-cyclohexanecarboxylate (1.4 g, 7.4 mmol) and THF (30 mL) was added LiAlH.sub.4 (0.57 g, 15 mmol). The mixture was stirred at 0° C. for 2 h, and 0.56 mL of H.sub.2O, 0.56 mL of 15% aqueous NaOH, and an additional 1.7 mL of H.sub.2O. The mixture was filtered, the filtrate was concentrated, added to H.sub.2O (10 mL), and extracted with EtOAc (2×15 mL). The combined extracts were washed with brine (15 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide (4-fluoro-4-methyl-cyclohexyl)methanol (0.80 g).
[0414] Step 4. A mixture of (4-fluoro-4-methyl-cyclohexyl)methanol (0.70 mg, 4.8 mmol), CH.sub.2Cl.sub.2 (20 mL), NaHCO.sub.3 (3.2 g, 38 mmol), and Dess-Martin periodinane (4.1 g, 9.6 mmol) was stirred at 25° C. for 2 hours. The mixture was poured into saturated NaHCO.sub.3 (5 mL) and saturated Na.sub.2SO.sub.3 (5 mL) and the resulting mixture was filtered and extracted with CH.sub.2Cl.sub.2 (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 4-fluoro-4-methyl-cyclohexanecarbaldehyde (0.60 mg).
Synthesis of 5″-nitrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline] (B-01)
[0415] ##STR00857##
[0416] Step 1. To a mixture of ZnEt.sub.2 (1 M in hexanes, 180 mL), CH.sub.2Cl.sub.2 (200 mL) at 0° C. under N.sub.2 was added slowly CH.sub.2I.sub.2 (26 mL, 320 mmol), in CH.sub.2Cl.sub.2 (60 mL). The mixture was stirred at 0° C. for 30 min and ethyl 4-methylenecyclohexanecarboxylate (12 g, 71 mmol) in CH.sub.2Cl.sub.2 (50 mL) was slowly added. The mixture was stirred at 20° C. for 12 h, cooled to 0° C., and saturated NH.sub.4Cl (100 mL) was added. The organic phase separated, washed with water (50 mL×2), brine (50 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (1-10% CH.sub.2C.sub.2 in petroleum ether) to afford the compound ethyl spiro[2.5]octane-6-carboxylate (10 g).
[0417] Step 2. To a mixture of ethyl spiro[2.5]octane-6-carboxylate (10 g, 55 mmol), THF (300 mL) at 0° C. under N.sub.2 was added LiAlH.sub.4 (3.1 g, 81 mmol) in portions. The mixture was stirred at 0° C. for 1 h, then at 22° C. for another 1 h. Aqueous 2M NaOH (3.0 mL) was slowly added to the stirring mixture, followed by Na.sub.2SO.sub.4 (30 g). The suspension was filtered, and the filtrate was concentrated to provide spiro[2.5]octan-6-ylmethanol (7.5 g). .sup.1H NMR (DMSO-d.sup.6, 400 MHz) δ 3.51 (d, J=6.38 Hz, 2H), 1.82-1.68 (m, 4H), 1.53 (tdt, J=14.71, 6.38, 3.24 Hz, 1H), 1.40-1.29 (m, 1H), 1.12-1.07 (m, 2H), 0.96-0.84 (m, 2H), 0.35-0.24 (m, 2H), 0.23-0.12 (m, 2H).
[0418] Step 3. To a mixture of spiro [2.5]octan-6-ylmethanol (7.5 g, 54 mmol) and CH.sub.2Cl.sub.2 (250 mL) was added Dess-Martin periodinane (28 g, 66 mmol) at 0° C. The mixture was stirred for 5 h as the temperature was allowed to rise to 25° C. The mixture was filtered through celite and the filter solid was washed with CH.sub.2Cl.sub.2 (50 mL×3). The filtrate was concentrated and purified by silica chromatography (0-10% EtOAc in petroleum ether) to provide spiro [2.5]octane-6-carbaldehyde (7.30 g). .sup.1H NMR (DMSO-d.sup.6, 400 MHz) δ 9.68 (d, J=1.25 Hz, 1H), 2.35-2.23 (m, 1H), 1.97-1.85 (m, 2H), 1.70-1.51 (m, 4H), 1.12-1.03 (m, 2H), 0.35-0.27 (m, 2H), 0.26-0.18 (m, 2H).
[0419] Step 4. a) A mixture of (4-nitrophenyl)hydrazine (1.8 g, 12 mmol), TFA (4.5 mL, 61 mmol), CH.sub.2Cl.sub.2 (40 mL), and spiro[2.5]octane-6-carbaldehyde (2.0 g, 15 mmol) was stirred at 40° C. for 15 h. b) Additional TFA (6.3 mL, 85 mmol), CH.sub.2Cl.sub.2, and Et.sub.3SiH (6.3 mL, 4.6 mmol) were added at 0° C. and the mixture stirred at 25° C. for 2 h, then was concentrated and purified by silica chromatography (0-15% [1:1 Me-THF in EtOAc] in petroleum ether) to provide 5″-nitrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline] (B-01, 0.88 g).
Synthesis of spiro[cyclopentane-1,3′-indoline] (B-02)
[0420] ##STR00858##
[0421] To a mixture of 1H-indole (1.0 g, 8.5 mmol) and THF (25 mL) was added dropwise t-BuOK (1 M in THF, 20 mL) and the mixture was stirred at 20° C. for 0.5 h. Et.sub.3B (1 M in THF, 17 mL) was added and the mixture was stirred for 0.5 h. 1,4-diiodobutane (1.2 mL, 9.4 mmol) was added and the mixture was stirred at 70° C. for 13 h. MeOH (10 mL) and NaBH.sub.4 (0.97 g, 26 mmol) were added and the mixture stirred at 20° C. for 12 h. The mixture was concentrated, combined with EtOAc (20 mL) and 2 N HCl (20 mL). The pH was adjusted to 9 by the slow addition of saturated aqueous NaHCO.sub.3. The phases were separated, and the aqueous wash was extracted with EtOAc (2×30 mL). The extracts were combined, washed with brine (10 mL), dried over Na.sub.2SO.sub.4, filtered, and concentrated to provide spiro[cyclopentane-1,3′-indoline] (B-02). .sup.1H NMR: (DMSO-d6, 400 MHz) δ 6.98 (dd, J=7.32, 0.81 Hz, 1H), 6.90 (td, J=7.57, 1.25 Hz, 1H), 6.55 (td, J=7.35, 0.94 Hz, 1H), 6.49 (d, J=7.75 Hz, 1H), 5.43 (s, 1H), 3.22 (s, 2H), 1.84-1.62 (m, 8H).
[0422] Compounds in Table 4 were prepared from the indole and dihalide in the manner described for B-02.
TABLE-US-00005 TABLE 4 Code Structure indole Amine B-03
Synthesis of dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline] (B-06)
[0423] ##STR00871##
[0424] Step 1. Dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indole] was prepared from phenylhydrazine and spiro[2.5]octane-6-carbaldehyde in the manner described in Step 4a of the synthesis of B-01.
[0425] Step 2. To a mixture of dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indole] (1.0 g, 4.7 mmol) in MeOH (15 mL) and THF (15 mL) at 0° C. was added NaBH.sub.3CN (0.90 g, 14 mmol) in portions. The mixture was stirred at 20° C. for 12 h and NaBH.sub.3CN (0.50 g) and THF (15 mL) was added, and the mixture was stirred at 40° C. for 2 h. The reaction mixture was concentrated and purified by chromatography (silica, 0-15% [1:1 THF/EtOAc] in petroleum ether) to afford dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline] (B-06, 0.64 g).
[0426] Compounds in Table 5 were prepared from the hydrazine and the aldehyde indicated by the method described for the synthesis of B-06.
TABLE-US-00006 TABLE 5 Code Structure Hydrazine Aldehyde B-07
Synthesis of tert-butyl 5″-bromodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carboxylate (B-10) and N-(dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)-2-hydroxyethane-1-sulfonamide (B-11)
[0427] ##STR00900##
[0428] Step 1. A mixture of B-07 (0.2 M, 3.4 mL) and Boc.sub.2O (0.30 g, 1.4 mmol), MeCN (10 mL), and Et.sub.3N (0.40 mL, 2.9 mmol) was stirred at 25° C. for 12 h. The mixture was concentrated and purified by silica chromatography (0-20% MTBE in petroleum ether) to provide tert-butyl 5″-bromo-1″,2″-dihydrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indole]-1″-carboxylate (B-10, 0.23 g).
[0429] Step 2. a) To a mixture of tert-butyl 5″-bromo-1″,2″-dihydrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indole]-1″-carboxylate (0.11 g, 0.27 mmol) and 2-[(tert-butyldimethylsilyl)oxy]ethane-1-sulfonamide (0.21 g, 0.88 mmol), and DMF (8.0 mL) was added CuI (57 mg, 0.30 mmol), K.sub.3PO.sub.4 (0.21 g, 0.99 mmol), and N.sup.1,N.sup.2-dimethylcyclohexane-1,2-diamine (48 mg, 0.34 mmol). The reaction mixture was stirred at 140° C. in a microwave reactor for 3 h. The reaction mixture was diluted with water 30 mL and extracted with 1:1 EtOAc/THF (15 mL×2). The extracts were combined, washed with H.sub.2O (10 mL×3) and brine (10 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (0-10% [1:1 THF/EtOAc] in petroleum ether) to provide 2-[(tert-butyldimethylsilyl)oxy]-N-{1″,2″-dihydrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indol]-5″-yl}ethane-1-sulfonamide (70 mg).
[0430] Step 3. A mixture of 2-[(tert-butyldimethylsilyl)oxy]-N-{1″,2″-dihydrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indol]-5″-yl}ethane-1-sulfonamide (60 mg, 0.11 mmol), MeOH (1.0 mL), and HCl (4 M in MeOH, 1.0 mL) was stirred at 25° C. for 5 h. The mixture was concentrated to provide N-{1″,2″-dihydrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indol]-5″-yl}-2-hydroxyethane-1-sulfonamide hydrochloride (B-11, 47 mg).
Separation of B-24 into Diastereomers
[0431] Indoline B-24 was separated into the (1s,4s) and (1r,4r) isomers by silica chromatography (0-100% EtOAc in PE). The configurations were not determined, and the first eluting isomer is B-24a and the second eluting isomer is B-24b.
Synthesis of tert-butyl 5′-bromospiro[cyclohexane-1,3′-indoline]-1′-carboxylate (B-12) and N-(spiro[cyclohexane-1,3′-indolin]-5′-yl)methanesulfonamide (B-13)
[0432] ##STR00901##
[0433] tert-Butyl 5′-bromospiro[cyclohexane-1,3′-indoline]-1′-carboxylate (B-12) and N-(spiro[cyclohexane-1,3′-indolin]-5′-yl)methanesulfonamide (B-13) were prepared from B-03 in the same manner as B-10 and B-11.
[0434] Intermediates in Table 5.1 were prepared from the indicated indolines and sulfonamides in the manner described for the synthesis of B-11.
TABLE-US-00007 TABLE 5.1 Code Structure Sulfonamide indoline B-14
Synthesis of spiro[cyclohexane-1,3′-indolin]-5′-ol hydrochloride (B-15)
[0435] ##STR00904##
[0436] Step 1. A mixture of B-12 (0.35 g, 0.96 mmol), NMP (8 mL), H.sub.2O (4 mL), was KOH (0.16 g, 2.9 mmol), Pd.sub.2(dba).sub.3 (88 mg, 96 μmol), di-tert-butyl-[2-(2,4,6-triisopropylphenyl)phenyl]phosphane (81 mg, 0.19 mmol) was stirred at 110° C. for 12 h, diluted with 10 mL of water, and extracted with EtOAc (5 mL×3). The combined extracts were washed with brine (5 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by preparative TLC (SiO.sub.2, 25% EtOAc in petroleum ether) to provide tert-butyl 5′-hydroxyspiro[cyclohexane-1,3′-indoline]-1′-carboxylate (80 mg).
[0437] Step 2. A mixture of tert-butyl tert-butyl 5′-hydroxyspiro[cyclohexane-1,3′-indoline]-1-carboxylate (80 mg, 0.26 mmol) and 1M HCl in EtOAc (2.0 mL) was stirred at 25° C. for 2 h, and was concentrated to provide spiro[cyclohexane-1,3′-indolin]-5′-ol hydrochloride (B-15; 60 mg).
Synthesis of 3-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonyl chloride (C-01)
[0438] ##STR00905##
[0439] Step 1. A mixture of 3-benzylsulfanylbenzoic acid (1.5 g, 6.1 mmol), DMF (10 mL), HATU (4.7 g, 13 mmol), and iPr.sub.2NEt (3.2 mL, 18 mmol) was stirred at 25° C. for 15 min and B-07 (1.8 g, 6.1 mmol) was added. The mixture was stirred at 25° C. for 2 h, then was diluted with EtOAc (50 mL), washed with water (30 mL×3) and brine (30 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (8-10% EtOAc in petroleum ether) to provide (3-(benzylthio)phenyl)(5″-bromodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-1″-yl)methanone (3.0 g).
[0440] Step 2. A mixture of (3-(benzylthio)phenyl)(5″-bromodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-1″-yl)methanone (2.0 g, 3.9 mmol), DMF (10 mL), methanesulfonamide (1.1 g, 12 mmol), K.sub.3PO.sub.4 (2.5 g, 12 mmol), N.sup.1,N.sup.2-dimethylcyclohexane-1,2-diamine (0.55 g, 3.9 mmol), and CuI (0.74 g, 3.9 mmol) was stirred at 160° C. for 2 h. The mixture was diluted with EtOAc (30 mL), washed with H.sub.2O (30 mL×3) and brine (30 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (29-31% EtOAc in petroleum ether) to provide N-(1″-(3-(benzylthio)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (1.84 g).
[0441] Step 3. A mixture of N-(1″-(3-(benzylthio)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (1.0 g, 1.9 mmol), NCS (0.50 g, 3.8 mmol), HOAc (1.8 mL), and H.sub.2O (0.2 mL) was stirred at 30° C. for 2 h. The mixture was diluted with EtOAc (50 mL), washed with H.sub.2O (30 mL×3), saturated aqueous NaHCO.sub.3 (30 mL), and brine (30 mL) before being dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (25-35% EtOAc in petroleum ether) to provide 3-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonyl chloride (C-01, 0.36 g).
[0442] Compounds in Table 5.2 were prepared from the indicated carboxylic acid and indoline in the same manner as described for C-01.
TABLE-US-00008 TABLE 5.2 Code Structure Carboxylic Acid Indoline C-03
Synthesis of 2-methoxy-5-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonyl chloride (C-02)
[0443] ##STR00912##
[0444] Step 1. A mixture of 3-benzylsulfanyl-4-methoxy-benzoic acid (0.32 mg, 1.2 mmol), B-14 (0.22 g, 0.73 mmol), DMF (3 mL), HOBt (0.26 g, 1.9 mmol), EDCI (0.37 g, 1.9 mmol), Et.sub.3N (0.54 mL, 3.9 mmol) was stirred at 25° C. for 2 h. The reaction was poured into H.sub.2O (30 mL), extracted with EtOAc (2×30 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (40-45% EtOAc in PE) to provide N-(1″-(3-(benzylthio)-4-methoxybenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.22 g).
[0445] Step 2. A mixture of N-(1″-(3-(benzylthio)-4-methoxybenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.22 g, 0.36 mmol), NCS (0.14 g, 1.1 mmol), H.sub.2O (0.05 mL), and HOAc (0.45 mL) was stirred at 25° C. for 2 h. The mixture was poured into H.sub.2O (10 mL) and saturated NaHCO.sub.3 (10 mL), extracted with EtOAc (2×30 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 2-methoxy-5-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonyl chloride (C-02, 0.20 g).
Synthetic Example S-001
Synthesis of (3-((4,4-difluoropiperidin-1-yl)sulfonyl)phenyl)(4′-fluorospiro[cyclopentane-1,3′-indolin]-1′-yl)methanone (Compound 1)
[0446] ##STR00913##
[0447] A mixture of 3-[(4, 4-difluoro-1-piperidyl)sulfonyl]benzoic acid (88 mg, 0.28 mmol), DMF (1.5 mL), Et.sub.3N (0.11 mL, 0.78 mmol), and HATU (0.20 g, 0.52 mmol) was stirred at 20° C. for 30 min, and 4′-fluorospiro [cyclopentane-1,3′-indoline] (50 mg, 0.26 mmol) in DMF (1.0 mL) was added. The resulting mixture was stirred at 20° C. for 3.5 h, concentrated, and purified by prep-HPLC (45-75% MeCN in H.sub.2O [10 mM NH.sub.4HCO.sub.3]) to afford (3-((4,4-difluoropiperidin-1-yl)sulfonyl)phenyl)(4′-fluorospiro[cyclopentane-1,3′-indolin]-1′-yl)methanone (Compound 1) (35 mg). ESI MS m/z: 479.2 (M+H).
[0448] Compounds in Table 6 were prepared from the carboxylic acid and indoline analog indicated by the method described for the synthesis of Compound 1 (Synthetic Example S-001).
TABLE-US-00009 TABLE 6 Compound Structure Carboxylic Acid Indoline Compound 2
Synthetic Example S-002
Synthesis of N-(1′-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)spiro[cyclopentane-1,3′-indolin]-5′-yl)methanesulfonamide (Compound 18)
[0449] ##STR01014##
[0450] A degassed mixture of Compound 2 (50 mg, 93 μmol), methanesulfonamide (13 mg, 0.14 mmol), CuI (9.0 mg, 46 μmol), K.sub.3PO.sub.4 (59 mg, 0.28 mmol), N.sup.1,N.sup.2-dimethylcyclohexane-1,2-diamine (7.0 mg, 46 μmol), and DMF (2.0 mL) was stirred at 150° C. for 2 h in a microwave reactor. The mixture was combined with H.sub.2O (30 mL) and extracted with EtOAc (2×30 mL). The extracts were combined, washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by prep-HPLC (35-0% H.sub.2O [10 mM NH.sub.4CO.sub.3] in MeCN) to provide N-(1′-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)spiro[cyclopentane-1,3′-indolin]-5′-yl)methanesulfonamide (Compound 18, 8.6 mg).
Synthetic Example S-002a
Synthesis of N-(tert-butyl)-3-(5″-(ethylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 134)
[0451] ##STR01015##
[0452] A degassed mixture of Compound 2 (1.0 g, 1.9 mmol), ethanesulfonamide (0.60 g, 5.5 mmol), CuI (0.37 g, 1.9 mmol), K.sub.3PO.sub.4 (1.3 g, 6.0 mmol), N.sup.1,N.sup.2-dimethylcyclohexane-1,2-diamine (0.27 g, 1.9 mmol), and DMF (14 mL) was stirred at 150° C. for 3 h. The mixture was combined with H.sub.2O (40 mL). The resulting precipitate was filtered, washed with H.sub.2O (5 mL×3), dissolved in EtOAc (50 mL), washed with water (20 mL×2), dried over Na.sub.2SO.sub.4, concentrated, and purified by prep-HPLC (50-20% H.sub.2O [0.100 formic acid] in MeCN) to provide N-(tert-butyl)-3-(5″-(ethyl sulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 134, 1.3 g).
[0453] Compounds in Table 7 were prepared from the indicated bromoindoline and primary sulfonamide in the same manner as Compound 18.
TABLE-US-00010 TABLE 7 Compound Structure Bromide Sulfonamide Compound 19
Synthesis of N-(tert-butyl)-3-(6″-fluoro-5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide and N-(tert-butyl)-3-(4″-fluoro-5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide
[0454] ##STR01198##
[0455] A ˜3/1 mixture Compound 307 and Compound 308 (0.55 g, 1.0 mmol), methanesulfonamide (0.29 g, 3.0 mmol), CuI (0.11 g, 0.60 mmol), DMF (5 mL), N1,N2-dimethylcyclohexane-1,2-diamine (85 mg, 0.60 mmol) and K.sub.3PO.sub.4 (0.64 g, 3.0 mmol) was stirred at 160° C. for 2 h. The mixture was concentrated, combined with H.sub.2O (10 mL), extracted with EtOAc (2×10 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (35-65% MeCN/H.sub.2O [formic acid]) to provide N-(tert-butyl)-3-(6″-fluoro-5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 309, 23.2 mg) and N-(tert-butyl)-3-(4″-fluoro-5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 310, 5.1 mg).
Synthetic Example S-002b
Synthesis of N-(tert-butyl)-2-methoxy-5-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 297) and N-(tert-butyl)-2-hydroxy-5-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 298)
[0456] ##STR01199##
[0457] A mixture of Compound 296 (0.10 g, 0.18 mmol), methanesulfonamide (51 mg, 0.53 mmol), CuI (34 mg, 0.18 mmol), K.sub.3PO.sub.4 (0.11 g, 0.53 mmol), N.sup.1,N.sup.2-dimethylcyclohexane-1,2-diamine (25 mg, 0.18 mmol), and DMF (2 mL) was stirred as 150° C. for 1.5 h. The mixture was then poured into 30 mL of H.sub.2O, extracted with EtOAc (2×30 mL) and the extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, filtered, concentration and purified by reverse-phase HPLC (C18, 30-60% MeCN/water [0.1 mM formic acid]) to provide 13 mg of Compound 297 and 26 mg of Compound 298.
Synthetic Example S-003
Synthesis of N-(1′-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)spiro[cyclopentane-1,3′-indolin]-5′-yl)-2-hydroxyethane-1-sulfonamide (Compound 27)
[0458] ##STR01200##
[0459] Step 1. A degassed mixture of Compound 2 (50 mg, 93 μmol), 2-((tert-butyldimethylsilyl)oxy)ethane-1-sulfonamide (33 mg, 0.14 mmol), CuI (9 mg, 46 μmol), K.sub.3PO.sub.4 (59 mg, 0.28 mmol) and N.sup.1,N.sup.2-dimethylcyclohexane-1,2-diamine (7 mg, 46 μmol), and DMF (2.0 mL) was stirred at 150° C. for 2 h in a microwave reactor. The mixture was poured into water H.sub.2O (30 mL) and extracted with EtOAc (2×30 mL). The extracts were combined, washed with brine (10 mL), dried over Na.sub.2SO.sub.4, and concentrated to provide 2-((tert-butyldimethylsilyl)oxy)-N-(1′-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)spiro[cyclopentane-1,3′-indolin]-5′-yl)ethane-1-sulfonamide (65 mg).
[0460] Step 2. A mixture of 2-((tert-butyldimethylsilyl)oxy)-N-(1′-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)spiro[cyclopentane-1,3′-indolin]-5′-yl)ethane-1-sulfonamide (65 mg, 93 μmol), MeOH (5.0 mL), and HCl (2M, 5.0 mL) was stirred at 20° C. for 1 h, concentrated, aqueous saturated NaHCO.sub.3 was added to bring the pH to 9. The mixture was extracted with EtOAc (2×30 mL) and the extracts were combined, washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by prep-HPLC (30-60% MeCN in H.sub.2O [10 mM NH.sub.4HCO.sub.3]) to provide N-(1′-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)spiro[cyclopentane-1,3′-indolin]-5′-yl)-2-hydroxyethane-1-sulfonamide (Compound 27, 8.5 mg).
[0461] Compounds in Table 7.1 were prepared from the indicated bromoindoline and 2-[(tert-butyldimethylsilyl)oxy]ethane-1-sulfonamide in the same manner as Compound 29.
TABLE-US-00011 TABLE 7.1 Compound Structure Bromoindole Compound 148
Synthetic Example S-004
Synthesis of N-(1″-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 28)
[0462] ##STR01210##
[0463] Step 1. To a mixture of Compound 12 (0.18 g, 0.33 mmol), and Fe (0.20 g, 3.6 mmol), EtOH (10 mL), THF (10 mL), and H.sub.2O (4.0 mL) was added NH.sub.4Cl (0.2 g, 3.7 mmol) and the mixture was stirred at 80° C. for 3 h. The mixture was filtered through celite, and the filter cake was washed with THF (10 mL×2) and MeOH (10 mL×2). The filtrate was concentrated to ˜20 mL, diluted with EtOAc (30 mL), washed with H.sub.2O (15 mL×2), brine (15 mL), dried over Na.sub.2SO.sub.4, filtered, and concentrated to (5″-aminodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-1″-yl)(3-((4,4-difluoropiperidin-1-yl)sulfonyl)phenyl)methanone (0.17 g).
[0464] Step 2. To a mixture of (5″-aminodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-1″-yl)(3-((4,4-difluoropiperidin-1-yl)sulfonyl)phenyl)methanone (0.15 g, 0.29 mmol), and Et.sub.3N (88 0.12 mL, 0.87 mmol), and CH.sub.2Cl.sub.2 (14 mL) was added slowly a mixture of methanesulfonyl chloride (68 μg, 0.87 mmol) and CH.sub.2Cl.sub.2 (1.0 mL) and the mixture was stirred at 20° C. for 2 h. The reaction mixture was poured into ice-water and extracted with CH.sub.2Cl.sub.2 (15 mL) and the extract was washed with H.sub.2O (5.0 mL×2) and brine (5.0 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by prep-HPLC (40-70% MeCN in water [0.1% formic acid]) to provide N-(1″-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 28, 55 mg).
Synthetic Example S-005
N-(1″-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)-2-hydroxyethane-1-sulfonamide (Compound 29)
[0465] ##STR01211##
[0466] A mixture of A-04 (16 mg, 53 μmol), DMF (1.0 mL), HATU (46 mg, 0.12 mmol) and iPr.sub.2NEt (18 μg, 0.10 mmol) was stirred at 25° C. for 15 min and a mixture of N-{1″,2″-dihydrodispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indol]-5″-yl}-2-hydroxyethane-1-sulfonamide (42 mg, 48 μmol), iPr.sub.2NEt (89 μg, 0.51 μmol), and DMF (1.0 mL) was added. After stirring at 25° C. for 5 h, the mixture was filtered and the filtrate was concentrated and purified by prep-HPLC (20-60% MeCN in H.sub.2O [0.1% formic acid]) to provide N-(1″-(3-((4,4-difluoropiperidin-1-yl)sulfonyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)-2-hydroxyethane-1-sulfonamide (Compound 29, 2 mg).
Synthetic Example S-006
Synthesis of (3-((4,4-difluoropiperidin-1-yl)sulfonyl)phenyl)(5″-(ethylamino)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-1″-yl)methanone (Compound 30)
[0467] ##STR01212##
[0468] A mixture of Compound 12 (0.15 g, 0.28 mmol), Pd/C (0.15 g, 10%) and EtOH (15 mL) was stirred under H.sub.2 (15 psi) at 25° C. for 12 h. The mixture was flushed with N.sub.2, filtered through celite, and the filtrate was concentrated and the minor product was isolated by prep-HPLC (45-80% MeCN in H.sub.2O [10 mM NH.sub.4HCO.sub.3]), and further by prep-HPLC (35-75% MeCN in H.sub.2O [0.1% formic acid]) to provide (3-((4,4-difluoropiperidin-1-yl)sulfonyl)phenyl)(5″-(ethylamino)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-1″-yl)methanone (Compound 30, 7.9 mg).
Synthetic Example S-007
Isolation of N-(tert-butyl)-3-(4-ethyl-5′-(methylsulfonamido)spiro[cyclohexane-1,3′-indolin]-3-en-1′-carbonyl)benzenesulfonamide (Compound 31)
[0469] ##STR01213##
[0470] Compound 31 was isolated as a side-product during the purification of Compound 22: prep-HPLC (40-60% MeCN in H.sub.2O [10 mM NH.sub.4HCO.sub.3].
Synthetic Example S-008
Preparation of N,N-dimethyl-3-(5′-(methylsulfonamido)spiro[cyclohexane-1,3′-indoline]-1′-carbonyl)benzenesulfonamide (Compound 42)
[0471] ##STR01214##
[0472] To a mixture of A-10 (50 mg, 0.22 mmol) and DMF (3 mL) were added HATU (0.12 g, 0.33 mmol) and iPr.sub.2NEt (0.11 mL, 0.65 mmol). After 20 min, B-13 (73 mg, 0.26 mmol) was added and the mixture was stirred at 60° C. for 2 h, concentrated, and purified by prep-HPLC (45-65% MeCN in H.sub.2O (0.1 M HCl)) to provide N,N-dimethyl-3-(5′-(methylsulfonamido)spiro [cyclohexane-1,3′-indoline]-1′-carbonyl)benzenesulfonamide (Compound 42, 50 mg).
[0473] Compounds in Table 7.2 were prepared from the indicated indoline and carboxylic acid in the same manner as Compound 42.
TABLE-US-00012 TABLE 7.2 Carboxylic Compound Structure Indoline acid Compound 166
Preparation of N-(1″-(3-(1-(4,4-difluoropiperidin-1-yl)ethyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 341)
[0474] ##STR01260##
[0475] A mixture of A-86 (0.55 g, 2.0 mmol), DMF (5.5 mL), Et.sub.3N (0.85 mL, 6.1 mmol), EDCI (1.4 g, 7.1 mmol), HOBt (0.96 g, 7.1 mmol) was stirred at 20° C. for 0.5 h, and then B-14 (0.25 g, 0.81 mmol) was added. The mixture was stirred at 20° C. for 12 h, poured into H.sub.2O (16 mL), and extracted with EtOAc (2×16 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 20-55% MeCN in H.sub.2O [formic acid]) provide N-(1″-(3-(1-(4,4-difluoropiperidin-1-yl)ethyl)benzoyl)dispiro [cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 341, 30 mg).
[0476] Compounds in Table 7.3 were prepared from the indicated indoline and carboxylic acid in the same manner as Compound 341.
TABLE-US-00013 TABLE 7.3 Carboxylic Code Structure Acid Indoline Example 344
Synthetic Example S-009
Preparation of ethyl (1′-(3-(piperidin-1-ylsulfonyl)benzoyl)spiro[cyclohexane-1,3′-indolin]-5′-yl)carbamate (Compound 141)
[0477] ##STR01279##
[0478] A mixture of Compound 142 (0.20 g, 0.39 mmol), dioxane (10 mL), Cs.sub.2CO.sub.3 (0.38 g, 1.2 mmol), Pd.sub.2(dba).sub.3 (35 mg, 39 μmol), Xantphos (22 mg, 39 μmol) and ethyl carbamate (52 mg, 0.58 mmol) was stirred at 110° C. for 12 h. The mixture was concentrated and purified by preparative HPLC (70-90% MeCN in H.sub.2O [0.1 M HCl]) to provide ethyl (1′-(3-(piperidin-1-ylsulfonyl)benzoyl)spiro[cyclohexane-1,3′-indolin]-5′-yl)carbamate (Compound 141, 21 mg).
Synthetic Example S-010
Preparation of N-(1′-(3-(cyclopentyl(hydroxy)methyl)benzoyl)spiro[cyclohexane-1,3′-indolin]-5′-yl)methanesulfonamide (Compound 157)
[0479] ##STR01280##
[0480] A degassed mixture of Compound 156 (0.10 g, 0.21 mmol), NaBH.sub.4 (16 mg, 0.42 mmol), and MeOH (2 mL) was stirred under an N.sub.2 atmosphere at 0° C. for 3 h. The mixture was concentrated and extracted with EtOAc (10 mL). The extract was washed with water (5 mL×2) and brine (3 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by preparative HPLC (42-72% MeCN in H.sub.2O [0.1% formic acid]) to provide N-(1′-(3-(cyclopentyl (hydroxy) methyl) benzoyl) spiro [cyclohexane-1, 3′-indolin]-5′-yl) methanesulfonamide (Compound 157, 20 mg).
[0481] Compounds in Table 7.4 were prepared from the indicated ketone in the manner described for the synthesis of Compound 157.
TABLE-US-00014 TABLE 7.4 Compound Structure Ketone Compound 165
Synthetic Example S-011
Preparation of N-(bicyclo[1.1.1]pentan-1-yl)-3-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide
[0482] ##STR01287##
[0483] To a mixture of bicyclo[1.1.1]pentan-1-amine (16 mg, 196 μmol), CH.sub.2Cl.sub.2 (1.0 mL) was added Et.sub.3N (82 μg, 0.59 mmol) and C-01 (100 mg, 0.20 mmol). The resulting mixture was stirred at 25° C. for 1 h, then was concentrated and partitioned between H.sub.2O (30 mL) and EtOAc (2×30 mL). The extracts were combined, washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (35-65% MeCN in H.sub.2O [0.1% formic acid]) to provide N-(bicyclo[1.1.1]pentan-1-yl)-3-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 223, 15 mg).
[0484] Compounds in Table 7.5 were prepared from the indicated sulfonyl chloride and amine in the same manner as Compound 223.
TABLE-US-00015 TABLE 7.5 Sulfonyl Compound Structure chloride amine Compound 224
Synthetic Example S-012
Preparation of N-(1′-(5-(cyclopentyl(hydroxy)methyl)thiophene-3-carbonyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 301)
[0485] ##STR01306##
[0486] Step 1. To a mixture of 5-formylthiophene-3-carboxylic acid (0.12 mg, 0.74 mmol) and DMF (1.5 mL) was added HATU (0.42 g, 1.1 mmol), and iPr.sub.2NEt (0.39 mL, 2.2 mmol). After stirring for 30 min, B-14 (0.27 mg, 0.88 mmol) was added and the mixture was stirred at 80° C. for 1.5 h, diluted with H.sub.2O (4 mL), and extracted with EtOAc (10 mL×3). The combined extracts were washed with brine (30 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (0-100% EtOAc/PE) to provide N-(1″-(5-formylthiophene-3-carbonyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.31 g). .sup.1H NMR (400 MHz, DMSO-d.sup.6) 6 ppm 10.00-9.91 (m, 1H) 8.14 (s, 1H) 8.08-7.96 (m, 1H) 7.26-7.19 (m, 2H) 7.15-7.00 (m, 1H) 4.08 (d, J=6.58 Hz, 2H) 2.98 (s, 3H) 1.27-1.24 (m, 8H) 0.36-0.28 (m, 4H).
[0487] Step 2. To a mixture of N-(1″-(5-formylthiophene-3-carbonyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.25 g, 0.56 mmol) and THF (3 mL) was added bromo(cyclopentyl)magnesium (1 M, 2.8 mL). The mixture was stirred at −70° C. for 2, slowly poured into ice (5 mL), and extracted with EtOAc (10 ml×3). The combined extracts were washed with brine (30 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 45%-75% MeCN in H.sub.2O [NH.sub.4HCO.sub.3]) to provide N-(1″-(5-(cyclopentyl(hydroxy)methyl)thiophene-3-carbonyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 301, 3.5 mg).
Preparation of N-(1″-(5-(cyclopentyl(hydroxy)methyl)furan-2-carbonyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 352)
[0488] ##STR01307##
[0489] Step 1. A mixture of 5-formylfuran-2-carboxylic acid (0.20 g, 1.4 mmol), DMF (3 mL), EDCI (0.55 g, 2.9 mmol), HOBt (0.39 g, 2.9 mmol), and iPr.sub.2Net (0.75 mL, 4.3 mmol) was stirred at 20° C. for 30 min., and B-14 (0.44 g, 1.4 mmol) in DMF (0.5 mL) was added dropwise at 20° C. The mixture was stirred at 20° C. for 12 h, poured into water (20 mL), and extracted with EtOAc (2×20 mL). The combined extracts were washed with brine (20 mL), dried over Na.sub.2SO.sub.4, concentrated, purified by silica chromatography (10-50% EtOAc in PE) to provide N-(1″-(3-formylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.23 g).
[0490] Step 2. To a mixture of N-(1″-(3-formylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.20 g, 0.37 mmol) and THF (3 mL) was added bromo(cyclopentyl)magnesium (1 M, 0.47 mL). The mixture was stirred at −60° C. for 0.5 h, poured into saturated NH.sub.4Cl (5 mL), and extracted with EtOAc (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, purified by preparative HPLC (C18, 30-70% MeCN in H.sub.2O [formic acid]) to provide N-(1″-(5-(cyclopentyl(hydroxy)methyl)furan-2-carbonyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 352, 7.0 mg).
Synthetic Example S-013
Preparation of N-(1″-(3-((3,3-difluoroazetidin-1-yl)sulfonyl)-4-hydroxybenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 303)
[0491] ##STR01308##
[0492] Two mixtures of Compound 302 (90 & 40 mg, 0.15 & 0.067 mmol), DMF (3 & 1.3 mL), LiCl (19 & 8.5 mg, 0.45 & 0.20 mmol) were stirred at 160° C. for 4 h. The mixtures were combined and poured into H.sub.2O (10 mL) and extracted with EtOAc (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 15-55% MeCN in H.sub.2O [NH.sub.4HCO.sub.3]) to provide N-(1″-(3-((3,3-difluoroazetidin-1-yl)sulfonyl)-4-hydroxybenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 303, 10 mg).
Synthetic Example S-014
Preparation of N-(1″-(3-(2-(3,3-difluoroazetidin-1-yl)-1-hydroxyethyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 314)
[0493] ##STR01309##
[0494] Step 1. A mixture of 3-vinylbenzoic acid (0.13 g, 0.89 mmol), DMF (3 mL), B-14 (0.30 mg, 0.98 mmol), HOBt (0.24 mg, 1.8 mmol), EDCI (0.34 g, 1.8 mmol), Et.sub.3N (0.37 mL, 2.7 mmol) was stirred at 20° C. for 2 h then poured into water (30 mL) and extracted with EtOAc (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-40% EtOAc in PE) to provide N-(1″-(3-vinylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.30 g).
[0495] Step 2. To a mixture of N-(1″-(3-vinylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.15 g, 0.34 mmol) and CH.sub.2Cl.sub.2 (1 mL) was added m-CPBA (0.14 g, 0.60 mmol, 85% purity) at 0° C. The mixture was stirred at 20° C. for 12 h, poured into Na.sub.2SO.sub.3 (1M, 30 mL), and extracted with EtOAc (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (0-30% EtOAc in PE) to provide N-(1″-(3-(oxiran-2-yl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.10 g).
[0496] Step 3. A mixture of 3,3-difluoroazetidine hydrochloride (39 mg, 0.30 mmol), iPr.sub.2NEt (0.10 mL, 0.60 mmol), EtOH (1 mL), and N-(1″-(3-(oxiran-2-yl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (90 mg, 0.20 mmol) was stirred at 80° C. for 12 h. The mixture was concentrated and purified by preparative HPLC (35-65% MeCN in H.sub.2O [formic acid]) to provide N-(1″-(3-(2-(3,3-difluoroazetidin-1-yl)-1-hydroxyethyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 314, 22 mg).
Preparation of N-(1″-(3-(2-(4,4-difluoropiperidin-1-yl)-1-hydroxyethyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 315)
[0497] ##STR01310##
[0498] (Compound 315) was prepared from N-(1″-(3-vinylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide and 3,3-difluoropiperidine hydrochloride by the method described for Compound 314.
Synthetic Example S-015
Preparation of N-(1″-(3-((piperidin-1-ylimino)methyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 318)
[0499] ##STR01311##
[0500] Step 1. Three mixtures of 3-formylbenzoic acid (0.20, 0.10, and 0.10 g, 1.3, 0.65, and 0.65 mmol), THF (10, 5, and 5 mL), EDCI (0.51, 0.25, and 0.25 g, 2.7, 1.4, and 1.4 mmol), HOBt (0.36, 0.18, and 0.18 g, 2.7. 1.4, and 1.4 mmol), Et.sub.3N (0.56, 0.28, and 0.28 mL, 4.0, 2.0, and 2.0 mmol) were stirred at this 20° C. for 0.5 h, and then B-14 (0.41, 0.21, 0.21 g, 1.3, 0.65, and 0.65 mmol) was added to the mixtures and they were stirred at 20° C. for 12 h. The mixtures were combined, poured into water (20 mL), and extracted with CH.sub.2Cl.sub.2 (2×20 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (20-100% EtOAc in PE) to provide N-(1″-(3-formylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.36 g).
[0501] Step 2. A mixture of N-(1″-(3-formylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.31 g, 0.73 mmol), EtOAc (3 mL), TFA (81 μg, 1.1 mmol), and piperidin-1-amine (0.47 g, 4.4 mmol) was stirred at 80° C. for 12 h. The mixture was concentrated, added to water (30 mL), and extracted with EtOAc (2×30 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 40-80% MeCN in H.sub.2O [formic acid]) to provide N-(1″-(3-((piperidin-1-ylimino)methyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.17 g).
Synthetic Example S-016
Preparation of N-(1″-(3-(1-cyclopentyl-1-hydroxyethyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 331)
[0502] ##STR01312##
[0503] To Compound 164 (50 mg, 99 μmol) in THF (1 mL) was added MeMgBr (3 M, 99 uL, 0.30 mmol) at 0° C. The mixture was stirred at 20° C. for 2 h, poured into H.sub.2O (3 mL), concentrated, and purified by preparative HPLC (40-80% MeCN in H.sub.2O [formic acid]) to provide N-(1″-(3-(1-cyclopentyl-1-hydroxyethyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 331, 6 mg).
Synthetic Example S-017
Preparation of N-(tert-butyl)-3-(5″-(1-hydroxyethyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 332)
[0504] ##STR01313##
[0505] Step 1. A degassed mixture of Compound 9 (0.20 g, 0.38 mmol), tributyl(1-ethoxyvinyl)stannane (0.19 mL, 0.56 mmol), Pd(PPh.sub.3).sub.2Cl.sub.2 (53 mg, 75 μmol), CsF (0.11 g, 0.75 mmol), and dioxane (4 mL) was stirred at 130° C. for 2 h under an N.sub.2 atmosphere. A solution of KF (0.10 g) in H.sub.2O (20 mL) and the mixture was stirred at 20° C. for 0.5 h. The mixture was extracted with EtOAc (20×2 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, filtered, concentrated, and purified by silica chromatography (0-50% EtOAc in PE) to provide 3-(5″-acetyldispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)-N-(tert-butyl)benzenesulfonamide (0.11 g).
[0506] Step 1. To a mixture of 3-(5″-acetyldispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)-N-(tert-butyl)benzenesulfonamide (0.11 g, 0.22 mmol) and MeOH (10 mL) was added NaBH.sub.4 (25 mg, 0.67 mmol) slowly at 0° C. The mixture was stirred at 0° C. for 3 h, poured into saturated NH.sub.4Cl (20 mL), and extracted with EtOAc (2×10 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 45-75% MeCN in H.sub.2O [formic acid]) to provide N-(tert-butyl)-3-(5″-(1-hydroxyethyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 332, 25 mg).
Synthetic Example S-018
Preparation of N-(1″-(3-((cyclobutylmethyl)sulfonyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 335)
[0507] ##STR01314##
[0508] A mixture of Compound 334 (0.20 g, 0.39 mmol), HOAc (2 mL), and 30% H.sub.2O.sub.2 (0.11 mL, 1.2 mmol) was stirred at 20° C. for 2 h. The mixture was combined with saturated Na.sub.2SO.sub.3 (20 mL) and H.sub.2O (30 mL) and extracted with EtOAc (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 35-65% MeCN in H.sub.2O [formic acid]) to provide N-(1″-(3-((cyclobutylmethyl)sulfonyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 335, 76 mg, 35.40% yield, 99.00% purity) as a white solid.
Synthetic Example S-019
Preparation of N-(tert-butyl)-3-(5″-(2,2,2-trifluoro-1-hydroxyethyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 338)
[0509] ##STR01315##
[0510] Step 1. A degassed mixture of Compound 9 (0.50 g, 0.94 mmol) and KBF.sub.3 (vinyl) (0.63 g, 4.7 mmol), K.sub.2CO.sub.3 (0.65 g, 4.7 mmol), PdCl.sub.2 (0.12 g, 0.66 mmol), and DMSO (5 mL) was stirred at 100° C. for 3 h under an N.sub.2 atmosphere. The mixture was poured into H.sub.2O (20 mL, extracted with CH.sub.2Cl.sub.2 (2×20 mL), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, purified by silica chromatography (30-50% EtOAc in PE) to provide N-(tert-butyl)-3-(5″-vinyldispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (0.32 mg).
[0511] Step 2. A mixture of N-(tert-butyl)-3-(5″-vinyldispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (0.32 g, 0.67 mmol), CH.sub.2Cl.sub.2 (10 mL), and MeOH (10 mL) was treated with 03 (32 mg, 669 umol, 1.0 eq) for 0.5 hour at 0° C. The solution was purged with 02 (21 mg, 669 umol, 1.0 eq) for 0.5 hour at 0° C., then stirred with PPh.sub.3 (0.35 g, 1.3 mmol) for 1 h at 20° C., poured into H.sub.2O (20 mL), and extracted with CH.sub.2Cl.sub.2 (2×20 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (30-50% EtOAc in PE) to provide N-(tert-butyl)-3-(5″-formyldispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (0.25 g).
[0512] Step 3. To a mixture of N-(tert-butyl)-3-(5″-formyldispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (0.15 g, 0.31 mmol) and DMF (2 mL) were added TMSCF.sub.3 (89 mg, 0.62 mmol) and CsF (95 mg, 0.62 mmol) at 50° C. The mixture was stirred at 50° C. for 12 h, concentrated, added to H.sub.2O (30 mL), and extracted with EtOAc (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC(C18, 35-75% MeCN in H.sub.2O [formic acid]) to provide N-(tert-butyl)-3-(5″-(2,2,2-trifluoro-1-hydroxyethyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 338, 11 mg).
Synthetic Example S-20
Preparation of N-(1″-(3-((3,3-difluoroazetidin-1-yl)methyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 345)
[0513] ##STR01316##
[0514] Step 1. A mixture of Compound 344 (0.28 g, 0.64 mmol), CH.sub.2Cl.sub.2 (5 mL), and PCC (0.27 g, 1.3 mmol) was stirred at 20° C. for 2 h, diluted with CH.sub.2Cl.sub.2 (10 mL), washed with H.sub.2O (5 mL), saturated aqueous NaHCO.sub.3 (5 mL), brine (5 mL), then dried over Na.sub.2SO.sub.4, concentrated, and purified by flash silica chromatography (0-50% EtOAc in PE) to provide N-(1″-(3-formylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.18 g).
[0515] Step 2. A mixture of N-(1″-(3-formylbenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.10 g, 0.23 mmol), MeOH (1 mL), THF (1 mL), 3,3-difluoroazetidine hydrochloride (44 mg, 0.34 mmol), and HOAc (26 μL, 0.46 mmol) was stirred at 20° C. for 2 h and NaBH.sub.3CN (43 mg, 0.68 mmol) was added and the mixture was stirred at 20° C. for 10 h. The mixture was treated with H.sub.2O (5 mL) at 0° C. and extracted with CH.sub.2Cl.sub.2 (10 mL). The combined extracts were washed with H.sub.2O (10 mL) and brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 25-65% MeCN in H.sub.2O [formic acid]) to provide N-(1″-(3-((3,3-difluoroazetidin-1-yl)methyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 345, 6 mg).
Synthetic Example S-21
Preparation of 2-methyl-N-(3-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)phenyl)propane-2-sulfonamide (Compound 355)
[0516] ##STR01317##
[0517] Step 1. A mixture of B-14 (0.20 g, 0.65 mmol), CH.sub.2Cl.sub.2 (4 mL), iPr.sub.2NEt (0.34 mL, 2.0 mmol) and 3-bromobenzoyl chloride (0.10 mL, 0.78 mmol) was stirred at 20° C. for 1 h and then concentration and poured into water (5 mL). The resulting mixture was extracted with EtOAc (10 mL×2) and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by silica chromatography (10-100% EtOAc in PE) to provide N-(1″-(3-bromobenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.21 g).
[0518] Step 2. A degassed mixture of N-(1″-(3-bromobenzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (0.10 g, 0.20 mmol), 2-methylpropane-2-sulfonamide (0.11 g, 0.82 mmol), CuI (78 mg, 0.41 mmol), N.sub.1,N.sub.2-dimethylcyclohexane-1,2-diamine dihydrochloride (88 mg, 0.41 mmol), K.sub.3PO.sub.4 (0.13 g, 0.61 mmol), and DMF (2 mL) was stirred at 160° C. for 2 h under an N.sub.2 atmosphere. The mixture was poured into water (10 mL), extracted with EtOAc (10 mL×2), and the combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 35-65% MeCN in H.sub.2O [NH.sub.4CO.sub.3]) to provide 2-methyl-N-(3-(5″-(methylsulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)phenyl)propane-2-sulfonamide (Compound 355, 16 mg).
Synthetic Example S-22
Preparation of N-(1″-(3-(1-hydroxy-3,3-dimethylbutyl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (Compound 357)
[0519] ##STR01318##
[0520] To mixture of N-(1″-(3-(oxiran-2-yl)benzoyl)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (50 mg, 0.11 mmol), CuCl2 (15 mg, 0.11 mmol), LiCl (5 mg, 0.11 mmol), and THF (1 mL) was added dropwise t-BuMgCI (1 M, 0.44 mL). The mixture was stirred at 20° C. for 2 h, poured into saturated aqueous NH.sub.4Cl (20 mL), and extracted with EtOAc (2×20 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, and purified by preparative HPLC (C18, 45-85% MeCN in H.sub.2O [formic acid]) to provide N-(1″-(3-(1-hydroxy-3,3-dimethylbutyl)benzoyl)dispiro [cyclopropane-1,1′-cyclohexane-4′,3″-indolin]-5″-yl)methanesulfonamide (8.0 mg).
Synthetic Example S-23
Preparation of N-(tert-butyl)-3-(5″-((2-fluoroethyl)sulfonamido)dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 365)
[0521] ##STR01319##
[0522] To a mixture of Compound 148 (50 mg, 87 μmol) in CH.sub.2Cl.sub.2 (1.5 mL) was added DAST (23 μL, 0.18 mmol) at 0° C. The mixture was stirred at 20° C. for 1 h under N.sub.2, poured into H.sub.2O (30 mL), and extracted with EtOAc (2×30 mL). The combined extracts were washed with brine (10 mL), dried over Na.sub.2SO.sub.4, concentrated, purified by preparative HPLC (C18, 45-75% MeCN in H.sub.2O [formic acid]) to provide N-(tert-butyl)-3-(5″-((2-fluoroethyl)sulfonamido) dispiro[cyclopropane-1,1′-cyclohexane-4′,3″-indoline]-1″-carbonyl)benzenesulfonamide (Compound 365, 13 mg).
[0523] Table 7c describes the chromatography separation of isomers for specific examples.
TABLE-US-00016 TABLE 7c Compound Conditions First Purity % Second Purity % 24 Chiralpak AD 24a .sup. 100% 24b 99.5% (250 mm × 30 mm, 10 μm) (er) (er) 15-40% [0.1% NH.sub.3/H.sub.2O in iPrOH] in supercritical CO.sub.2 140 Chiralpak AD 140a .sup. 100% 140b 99.5% (250 mm × 30 mm, 10 μm) 45-75% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 162 Phenomenex Luna C18 162a .sup. 100% 162b 100% (200 × 40 mm, 10 μm) 30-60% MeCN in H.sub.2O [0.1M formic acid] 165 Chiralpak AD 165a >99.5% 165b 98.9% (250 mm × 30 mm, 10 μm) (er) (er) 35% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 249 Chiralpak OD (R)-249 .sup. 100% (S)-249 98.9% (250 mm × 30 mm, 10 μm) (er) (er) 45% [0.1% NH.sub.3/H.sub.2O in iPrOH] in supercritical CO.sub.2 287 Regis (S,S)-Whelk-O ®1 287a 99.7% 287b 97.8% (250 mm × 25 mm, 10 μm) (er) (er) 60% EtOH in supercritical CO.sub.2 305 Chiralcel OD 305a 99.7% 205b 99.0% (250 mm × 30 mm, 10 μm) (er) (er) 44% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 313 Chiralpak AD 313a >99.5% 313b 99.2% (250 mm × 30 mm, 10 μm) (er) (er) 35% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 316 Chiralcel OD 316a >99.5% 316b 99.7% (250 mm × 30 mm, 10 μm) (er) (er) 45% [0.1% NH.sub.3/H.sub.2O in iPrOH] in supercritical CO.sub.2 317 Chiralcel OD 317a >99.5% 317b 98.7 (250 mm × 30 mm, 10 μm) (er) (er) 40% [0.1% NH.sub.3/H.sub.2O in iPrOH] in supercritical CO.sub.2 333 Phenomenex Luna C18 333a .sup. 100% 333b 100% (100 × 40 mm, 3 μm) 20-60% MeCN in H.sub.2O [0.1M formic acid] 336 Phenomenex Luna C18 336a .sup. 100% 336b 100% (200 × 40 mm, 10 μm) 45-80% MeCN in H.sub.2O [0.1M formic acid] 338 Chiralpak AD 338a >99.9% 338b 99.2% (250 mm × 30 mm, 10 μm) (er) (er) 27-75% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 341 Chiralpak AD 341a >99.9% 341b 99.8% (250 mm × 30 mm, 10 μm) (er) (er) 25% [0.1% NH.sub.3/H.sub.2O in iPrOH] in supercritical CO.sub.2 351 Chiralpak IC 351a 99.9% 351a 99.2% (250 mm × 30 mm, 10 μm) (er) (er) 50% [0.1% NH.sub.3/H.sub.2O in iPrOH] in supercritical CO.sub.2 352 Chiralpak AD 352a >99.9% 352b >99.95% (250 mm × 30 mm, 10 μm) (er) (er) 40% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 367 Chiralpak AD 367a >99.9% 367b >99.9% (250 mm × 30 mm, 10 μm) (er) (er) 40% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 368 Chiralpak AD 368a >99.9% 368b >99.9% (250 mm × 30 mm, 10 μm) (er) (er) 40% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 371 Chiralpak AD 371a >99.9% 371b 98.6% (250 mm × 30 mm, 10 μm) (er) (er) 22% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2 372 Chiralcel OJ 372a >99.9% 372b 99.9% (250 mm × 30 mm, 10 μm) (er) (er) 30% [0.1% NH.sub.3/H.sub.2O in MeOH] in supercritical CO.sub.2 373 Chiralpak AD 373a >99.9% 373b 99.3% (250 mm × 30 mm, 10 μm) (er) (er) 30% [0.1% NH.sub.3/H.sub.2O in EtOH] in supercritical CO.sub.2
TABLE-US-00017 TABLE 8 Compound ESI MS (M/z) NMR summary (400 MHz) ppm Compound 1 479.2 (DMSO-d.sup.6) δ 7.98 (dt, J = 15.13, 7.44 Hz, 4H), 7.86-7.77 (m, 1H), (M + H) 7.29 (br s, 1H), 6.94 (br t, J = 8.94 Hz, 1H), 3.85 (br s, 2H), 3.33 (s, 1H), 3.15 (br d, J = 5.00 Hz, 4H), 2.14-1.96 (m, 6H), 1.86 (br s, 2H), 1.77 (br s, 2H), 1.56 (br s, 2H). Compound 2 (DMSO-d.sup.6) δ 8.11-7.89 (m, 3H), 7.85-7.77 (m, 1H), 7.51 (d, J = 2.00 Hz, 2H), 3.82 (br s, 2H), 3.21-3.09 (m, 4H), 2.16-1.98 (m, 4H), 1.91-1.70 (m, 6H), 1.66-1.43 (m, 2H) Compound 3 461.1 (DMSO-d.sup.6) δ 8.33-7.83 (m, 3H), 7.83-7.74 (m, 1H), 7.45-6.95 (m, (M + H).sup.+ 3H), 3.85-3.72 (m, 2H), 3.12 (br d, J = 4.88 Hz, 4H), 2.13-1.98 (m, 4H), 1.87-1.69 (m, 6H), 1.65-1.48 (m, 2H). Compound 4 501.1 (DMSO-d.sup.6) δ 7.88-8.27 (m, 4 H) 7.77-7.85 (m, 1 H) 7.31 (br d, (M + H).sup.+ J = 7.82 Hz, 1 H) 6.98-7.30 (m, 1 H) 6.98-7.30 (m, 1 H) 3.89 (br s, 2 H) 3.13 (br s, 4 H) 2.01-2.12 (m, 4 H) 1.36-1.90 (m, 6 H) 0.85 (br d, J = 10.64 Hz, 2 H) 0.26 (br s, 4 H) Compound 6 465.1 (DMSO-d.sup.6) δ 8.21-7.86 (m, 4H) 7.83-7.73 (m, 1H), 7.31 (d, J = (M + H).sup.+ 7.88 Hz, 2H) 7.11 (br d, J = 2.25 Hz, 1H), 3.92 (br s, 2 H) 2.98- 2.88 (m, 4H), 1.77-1.62 (m, 5 H), 1.55 (br s, 5H), 1.41-1.32 (m, 2H), 0.93-0.79 (m, 2H), 0.33-0.20 (m, 4H). Compound 8 451.1 (DMSO-d.sup.6) δ 8.22-7.85 (m, 4H), 7.80-7.73 (m, 1H), 7.30 (d, J = (M + H).sup.+ 8.38 Hz, 2H), 7.10 (m, 1H), 3.95-3.82 (m, 2H), 3.18 (br s, 4H), 1.79-1.50 (m, 10H), 0.93-0.78 (m, 2H), 0.34-0.17 (m, 4H). Compound 9 (DMSO-d.sup.6) δ 8.04 (s, 1H), 7.99 (d, J = 7.2 Hz 2H), 7.85 (d, J = 7.2 Hz, 1H), 7.73-7.69 (t, J = 7.2 Hz, 1H), 7.67 (s, 1H), 7.51 (s, 1H), 7.41 (br s, 1H), 3.90 (s, 2H), 1.77-1.74 (m, 2H), 1.65-1.62 (m, 4H), 1.11 (s, 9H), 0.84-0.81 (br d, J = 12.8 Hz, 2H), 0.26 (m, 4H) Compound 10 453.1 (DMSO-d.sup.6) δ 8.19-7.92 (m, 3H) 7.83 (br d, J = 5.63 Hz, 1H) 7.75- (M + H).sup.+ 7.60 (m, 2H), 7.31 (d, J = 8.25 Hz, 2H), 7.10 (br s, 1H), 3.92-3.83 (m, 2H), 1.81-1.55 (m, 6H), 1.10 (s, 9H) 0.88-0.81 (m, 2H), 0.26 (br s, 4H) Compound 15 567.0 (DMSO-d.sup.6) δ 8.12-7.91 (m, 4H), 7.87-7.76 (m, 1H), 7.66 (s, 1H), (M + H).sup.+ 7.53-7.35 (m, 1H), 3.92-3.75 (m, 2H), 3.19-3.06 (m, 4H), 2.15- 1.99 (m, 4H), 1.85-1.77 (m, 1H), 1.71-1.31 (m, 8H), 1.04 (br d, J = 6.8 Hz, 1H), 0.90-0.73 (m, 3H) Compound 18 554.0 (CD3OD) δ 8.23-7.96 (m, 3H), 7.93 (br d, J = 5.63 Hz, 1H), 7.85- (M + H).sup.+ 7.77 (m, 1H), 7.32-6.96 (m, 2H), 4.09-3.83 (m, 2H), 3.26 (br s, 4H), 2.96 (br s, 3H), 2.18-2.04 (m, 4H), 1.89 (br s, 6H), 1.80-1.57 (m, 2H). Compound 19 568.1 (DMSO-d.sup.6) δ 9.57 (br s, 1H), 8.09-8.08 (m, 1H), 8.10-7.89 (m, (M + H).sup.+ 4H), 7.87-7.75 (m, 1H), 7.11 (s, 2H), 3.84 (br s, 2H), 3.13 (br s, 4H), 2.94 (s, 3H), 2.14-1.97 (m, 4H), 1.77-1.45 (m, 8H), 1.24 (br s, 1H), 1.13 (br d, J = 14.26 Hz, 1H) Compound 20 558.1 (DMSO-d.sup.6) δ 9.58 (br d, J = 2.13 Hz, 1H), 8.12-7.84 (m, 4H), (M + H).sup.+ 7.82-7.75 (m, 1H), 7.13 (d, J = 1.75 Hz, 2H), 3.92 (br s, 2H), 2.94 (s, 7H), 1.72-1.49 (m, 10H), 1.37 (br d, J = 5.00 Hz, 2H), 0.96- 0.79 (m, 2H), 0.35-0.19 (m, 4H). Compound 21 544.1 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.11-7.89 (m, 4H), 7.82-7.73 (m, (M + H).sup.+ 1H), 7.18-7.03 (m, 2H), 3.90 (br d, J = 2.88 Hz, 2H), 3.22-3.16 (m, 4H), 2.94 (s, 3H), 1.74-1.49 (m, 10H), 0.94-0.80 (m, 2H), 0.28 (br s, 4H). Compound 22 546.1 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.11-7.91 (m, 3H), 7.88-7.67 (m, (M + H).sup.+ 1H), 7.74-7.59 (m, 2H), 7.14 (d, J = 1.88 Hz, 2H ) 3.88 (br d, J = 1.63 Hz, 2H), 2.94 (s, 3H), 1.74-1.49 (m, 6H), 1.11 (s, 9H), 0.94- 0.80 (m, 2H), 0.34-0.18 (m, 4H). Compound 23 568.1 (DMSO-d.sup.6) δ 9.67-9.54 (m, 1H), 8.17-7.89 (m, 4H), 7.86-7.73 (m, (M + H).sup.+ 1H), 7.02 (br d, J = 3.5 Hz, 2H), 3.96-3.75 (m, 2H), 3.22-3.06 (m, 4H), 2.95 (s, 3H), 2.16-2.01 (m, 6H), 1.99-1.90 (m, 2H), 1.85-1.77 (m, 1H), 1.72-1.61 (m, 1H), 1.47-1.28 (m, 1H), 1.20-1.08 (m, 1H), 1.07-0.92 (m, 3H) Compound 24 582.1 (DMSO-d.sup.6) δ 9.24-9.51 (m, 1H), 7.72-8.05 (m, 4H), 7.35-7.42 (m, (M + H).sup.+ 1H), 7.19-6.99 (m, 2H), 3.95-3.70 (m, 2H), 3.28-3.18 (m, 3H), 2.99-2.91 (m, 4H), 2.17-1.98 (m, 4H), 1.77-1.57 (m, 6H), 1.52- 1.35 (m, 2H), 1.04 (d, J = 6.7 Hz, 1H), 0.91-0.76 ppm (m, 3H) Compound 24a 582.1 (DMSO-d.sup.6) δ 9.52 (s, 1H), 8.15-7.89 (m, 4H), 7.86-7.73 (m, 1H), (M + H).sup.+ 7.35 (d, J = 1.9 Hz, 1H), 7.22-7.03 (m, 1H), 3.88-3.67 (m, 2H), 3.19-3.07 (m, 4H), 2.95 (s, 3H), 2.14-2.00 (m, 5H), 1.81-1.70 (m, 2H), 1.66-1.57 (m, 1H), 1.54-1.34 (m, 6H), 1.06-0.96 (m, 3H) Compound 24b 582.1 (DMSO-d.sup.6) δ 9.65-9.54 (m, 1H), 8.12-7.89 (m, 4H), 7.84-7.77 (m, (M + H).sup.+ 1H), 7.09 (d, J = 1.9 Hz, 2H), 3.95-3.75 (m, 2H), 3.19-3.09 (m, 4H), 2.94 (s, 3H), 2.13-1.96 (m, 5H), 1.74-1.52 (m, 7H), 1.47-1.37 (m, 2H), 0.87-0.75 (m, 3H) Compound 25 530.1 (DMSO-d.sup.6) δ 8.32-8.09 (m, 1H), 8.03-7.87 (m, 2H), 7.80 (br d, J = (M + H).sup.+ 7.25 Hz, 1H), 7.74-7.63 (m, 1H), 7.19-7.12 (m, 1H), 7.10-6.93 (m, 1H), 6.49-6.37 (m, 1H), 3.99-3.70 (m, 2H), 3.63-3.49 (m, 2H), 3.22-3.08 (m, 2H), 3.04-2.93 (m, 3H), 1.80-1.62 (m, 8H), 1.50- 1.44 (m, 2H), 1.38-1.23 (m, 2H), 0.66-0.56 (m, 1H), 0.39-0.31 (m, 1H) Compound 26 520.1 (DMSO-d.sup.6) δ 8.32-7.92 (m, 3H), 7.81-7.70 (m, 1H), 7.68-7.57 (m, (M + H).sup.+ 1H), 7.21-7.11 (m, 1H), 7.08-6.90 (m, 1H), 6.65-6.43 (m, 1H), 4.85-4.51 (m, 1H), 4.06-3.65 (m, 2H), 3.07-2.91 (m, 3H), 1.71 (br d, J = 11.88 Hz, 10H), 1.28-1.21 (m, 9H) Compound 27 558.1 (DMSO-d.sup.6) δ 8.10 (br d, J = 2.13 Hz, 4H), 7.84-7.69 (m, 1H), (M + H).sup.+ 7.21-6.94 (m, 2H), 3.91-3.76 (m, 2H), 3.73 (br t, J = 6.57 Hz, 2H), 3.19-3.05 (m, 6H), 2.14-1.99 (m, 4H), 1.92-1.69 (m, 6H), 1.63- 1.44 (m, 2H). Compound 28 594.1 (DMSO-d.sup.6) δ 9.68-9.48 (m, 1H), 8.21-7.88 (m, 1H), 8.15-7.88 (m, (M + H).sup.+ 3H), 7.86-7.74 (m, 1H), 7.13 (br d, J = 1.75 Hz, 2H), 4.02-3.79 (m, 2H), 3.13 (br s, 4H), 3.02-2.84 (m, 3H), 2.17-1.97 (m, 3H), 2.15-1.96 (m, 1H), 1.76-1.62 (m, 1H), 1.74-1.48 (m, 1H), 1.67 (br s, 4H), 0.93-0.78 (m, 2H), 0.27 (br s, 3H), 0.37-0.12 (m, 1H) Compound 29 624.0 (DMSO-d.sup.6) δ 8.17 (br d, J = 7.25 Hz, 1H), 8.03-7.89 (m, 2H), 7.84 (M + H).sup.+ (br d, J = 7.50 Hz, 1H), 7.75-7.67 (m, 1H), 7.25 (d, J = 1.88 Hz, 1H), 7.20-6.99 (m, 1H), 6.67 (br s, 1H), 4.13 (br t, J = 4.88 Hz, 1H), 3.89 (br s, 2H), 3.25 (br s, 6H), 2.51 (br s, 1H), 2.18-2.03 (m, 4H), 1.90-1.80 (m, 2H), 1.69 (br d, J = 12.26 Hz, 4H), 0.94 (br d, J = 11.76 Hz, 2H), 0.32 (br s, 4H) Compound 30 544.1 (DMSO-d.sup.6) δ 8.39-8.30 (m, 1H), 8.01-7.83 (m, 3H), 7.82-7.75 (m, (M + H).sup.+ 1H), 8.02-7.73 (m, 1H), 6.49 (d, J = 2.13 Hz, 1H), 6.44 (br d, J = 8.00 Hz, 1H), 5.50-5.39 (m, 1H), 3.84-3.75 (m, 1H), 3.79 (s, 1H), 3.16-3.09 (m, 1H), 3.16-3.08 (m, 1H), 3.13 (br s, 2H), 3.07-2.98 (m, 2H), 2.14-1.98 (m, 4H), 1.75-1.47 (m, 6H), 1.16 (br t, J = 7.00 Hz, 2H), 1.22-1.03 (m, 1H), 0.83 (br d, J = 12.76 Hz, 2H), 0.41- 0.16 (m, 1H), 0.23 (br d, J = 6.13 Hz, 3H) Compound 31 546.1 (DMSO-d.sup.6) δ 7.92-8.02 (m, 2H), 7.81-7.74 (m, 1H), 7.72-7.64 (m, (M + H).sup.+ 1H), 7.38 (br s, 1H), 7.12 (s, 1H), 7.05 (br s, 1H), 5.39 (br s, 1H), 3.84-3.67 (m, 2H), 2.92 (s, 3H), 2.29-2.10 (m, 2H), 1.90-2.08 (m, 4H), 1.88-1.77 (m, 1H), 1.69-1.59 (m, 1H), 1.15 (s, 9H), 0.98-0.94 (m, 3H) Compound 32 622.2 (CDCl.sub.3) δ 8.38-8.11 (m, 1H), 7.97 (br s, 1H), 7.93 (br d, J = 7.75 (M + H).sup.+ Hz, 1H), 7.84 (br d, J = 7.51 Hz, 1H), 7.76-7.65 (m, 1H), 7.26- 7.08 (m, 2H), 4.06-3.81 (m, 2H), 3.73 (br d, J = 6.91 Hz, 2H), 3.26 (br t, J = 5.30 Hz, 4H), 2.90 (s, 3H), 2.18-2.03 (m, 4H), 1.92-1.79 (m, 2H), 1.72 (br d, J = 11.80 Hz, 4H), 1.16 (br t, J = 7.03 Hz, 3H), 0.96 (br s, 2H), 0.33 (s, 4H) Compound 42 492.0 (DMSO-d.sup.6) δ 9.77-9.41 (m, 1H), 8.15-7.83 (m, 4H), 7.82-7.75 (m, (M + H).sup.+ 1H), 7.15-7.00 (m, 2H), 3.93-3.79 (m, 2H), 2.98-2.88 (m, 3H), 2.64 (s, 6H), 1.79-1.43 (m, 7H), 1.38-0.89 (m, 3H) Compound 43 501.1 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.14-7.97 (m, 1H), 7.95-7.85 (m, (M + H).sup.+ 1H), 7.81 (br d, J = 7.1 Hz, 1H), 7.78-7.67 (m, 2H), 7.19-6.96 (m, 2H), 3.95-3.79 (m, 2H), 3.39-3.29 (m, 1H), 2.99-2.90 (m, 3H), 1.97-1.78 (m, 3H), 1.67-1.39(m, 12H), 1.34-1.05 (m, 3H) Compound 45 504.1 (DMSO-d.sup.6) δ 8.31-8.10 (br s, 1H), 8.09-7.95 (m, 2H), 7.85 (br d, J = (M + H).sup.+ 7.6 Hz, 1H), 7.75-7.71 (m, 1H), 7.16 (s, 1H), 7.10-6.90 (br s, 1H), 6.36 (br s, 1H), 4.25-3.68 (m, 6H), 2.99 (s, 3H), 2.20-2.07 (m, 2H), 1.88-1.62 (m, 7H), 1.40-1.10 (m, 3H Compound 46 504.2 (DMSO-d.sup.6) δ 9.73-9.40 (m, 1H), 8.18-7.82 (m, 5H), 7.81-7.72 (m, (M + H).sup.+ 1H), 7.23-7.00 (m, 2H), 3.99-3.79 (m, 2H), 3.05-2.86 (m, 3H), 2.22-2.12 (m, 1H), 1.74-1.47 (m, 7H), 1.35-1.01 (m, 3H), 0.55- 0.44 (m, 2H), 0.41-0.31 (m, 2H) Compound 48 506.0 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.35-7.91 (m, 3H), 7.90-7.80 (m, (M + H).sup.+ 1H), 7.77-7.63 (m, 2H), 7.20-6.92 (m, 2H), 3.97-3.65 (m, 2H), 3.06-2.81 (m, 3H), 1.75-1.59 (m, 4H), 1.58-1.40 (m, 3H), 1.35- 1.04 (m, 3H), 1.02-0.87 (m, 6H) Compound 49 516.1 (DMSO-d.sup.6) δ 9.68-9.49 (brs, 1H), 8.08-8.02 (m, 3H), 7.93-7.85 (M + H).sup.+ (m, 1H), 7.76-7.72 (m, 1H), 7.11-6.99 (m, 2H), 4.30 (s, 1H), 3.90- 3.79 (m, 2H), 3.72-3.63 (m, 1H), 3.42 (m, 1H), 2.93 (s, 3H), 1.94- 1.70 (m, 4H), 1.64-1.52 (m, 12H), 1.27 (m, 1H), 1.24-1.23 (m, 1H) Compound 50 517.0 (CDCl.sub.3) δ 8.40-7.95 (m, 3H), 7.90-7.81 (m, 1H), 7.77-7.67 (m, (M + H)+ 1H), 7.20-7.12 (m, 1H), 7.11-6.9 (m, 1H), 6.36-6.24 (m, 1H), 4.15-3.75 (m, 2H), 3.59-3.48 (m, 1H), 3.01-2.98 (m, 3H), 2.15- 2.01 (m, 2H), 1.98-1.64 (m, 14H), 1.31-1.22 (m, 2H) Compound 55 520.1 (DMSO-d.sup.6) δ 9.67-9.51 (m, 1H), 8.10-7.87 (m, 3H), 7.78-7.70 (m, (M + H).sup.+ 1H), 7.23-6.99 (m, 2H), 4.15-4.02 (m, 1H), 3.94-3.77 (m, 2H), 3.02-2.86 (m, 3H), 2.79-2.64 (m, 3H), 1.77-1.47 (m, 7H), 1.34- 1.03 (m, 3H), 0.98-0.81 (m, 6H) Compound 57 524.2 (DMSO-d.sup.6) δ 9.60 (brs, 1H), 7.99 (m, 1H), 7.61 (s, 1H), 7.36 (s, (M + H).sup.+ 1H), 7.12 (d, J = 2.0 Hz, 2H), 7.07-7.05 (m, 1H), 4.21 (s, 2H), 2.95 (s, 3H), 2.58 (s, 3H), 1.73-1.49 (m, 6H), 1.44-1.26 (m, 4H), 1.24-1.13 (m, 9H) Compound 59 541.3 (DMSO-d.sup.6) δ 9.69-9.55 (m, 1H), 8.15-7.97 (m, 1H), 7.66-7.60 (m, (M + NH.sub.4).sup.+ 1H), 7.27-7.17 (m, 1H), 7.13 (s, 1H), 7.13 (s, 1H), 4.04 (s, 2H), 4.00 (s, 3H), 2.95 (s, 3H), 1.78-1.59 (m, 5H), 1.55-1.43 (m, 2H), 1.37-1.21 (m, 3H), 1.17 (s, 9H) Compound 60 526.0 (CDCl.sub.3) δ 8.10-8.01 (brs, 1H), 7.60 (d, J = 3.6 Hz, 1H), 7.50 (br d, (M + H).sup.+ J = 3.2 Hz, 1H), 7.18 (s, 1H), 7.04-7.02 (d, J = 8.0 Hz, 1H), 6.52 (s, 1H), 4.76 (s, 1H), 4.16 (s, 2H), 3.00 (s, 3H), 1.78-1.65 (m, 8H), 1.59 (m, 1H), 1.35 (s, 9H), 1.26 (s, 1H) Compound 67 530.1 (CDCl.sub.3) δ 8.25-8.00 (m, 3H), 7.91 (d, J = 7.63 Hz, 1H) 7.83-7.72 (M + H).sup.+ (m, 1 H), 7.16-7.08 (m, 1H), 6.54-6.35 (m, 1H), 3.94-3.74 (m, 2H), 2.98-2.93 (m, 2H), 2.36-2.11 (m, 3H), 1.72-1.55 (m, 10H), 1.50-0.92 (m, 5H) Compound 70 531.1 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.15-7.85 (m, 4H), 7.85-7.76 (m, (M + H).sup.+ 1H), 7.2-6.92 (m, 2H), 3.85 (br s, 2H), 3.30 (br s, 1H), 2.94 (s, 3H), 2.00-1.89 (m, 2H), 1.78-1.70 (m, 2H), 1.70-1.47 (m, 8H), 1.34-1.05 (m, 8H) Compound 71 532.1 (DMSO-d.sup.6) δ 9.64-9.52 (m, 1H), 8.18-7.84 (m, 4H), 7.82-7.72 (m, (M + H).sup.+ 1H), 7.16-7.02 (m, 2H), 3.93-3.76 (m, 2H), 3.25-3.14 (m, 2H), 2.94 (s, 3H), 2.78-2.62 (m, 2H), 2.11-1.95 (m, 1H), 1.92-1.79 (m, 1H), 1.72-1.44 (m, 7H), 1.35-1.02 (m, 4H), 0.84-0.74 (m, 3H Compound 83 536.1 (CDCl.sub.3) δ 8.36-8.07 (m, 1H), 8.06-7.90 (m, 2H), 7.88-7.77 (m, (M + H).sup.+ 1H), 7.74-7.60 (m, 1H), 7.22-6.90 (m, 2H), 6.69-6.38 (m, 1H), 5.31-5.02 (m, 1H), s3.85 (br d, J = 3.25 Hz, 2H), 3.69-3.48 (m, 3H), 3.42-3.21 (m, 1H), 2.99 (br s, 3H), 2.27-2.14 (m, 1H), 2.09- 1.88 (m, 1H), 1.71 (br d, J = 11.01 Hz, 7H), 1.38-1.02 (m, 3H) Compound 95 538.0 (DMSO-d.sup.6) δ 9.60 (s, 1H), 8.06-7.96 (m, 1H), 7.91-7.85 (m, 1H), (M + H).sup.+ 7.80-7.74 (m, 3H), 7.15-7.06 (m, 2H), 3.82 (m, 2H), 2.94 (s, 3H), 1.62-1.52 (m, 8H), 1.28-1.21 (m, 2H), 1.13 (s, 9H) Compound 96 538.1 (CDCl.sub.3) δ 8.15-8.10 (m, 1H), 7.87-7.79 (m, 1H), 7.35-7.31 (m, (M + H).sup.+ 1H), 7.21-7.15 (m, 2H), 7.00 (m, 1H), 6.24 (s, 1H), 4.79 (s, 1H), 3.91-3.80 (m, 2H), 2.99 (s, 3H), 1.76-1.62 (m, 7H), 1.35-1.31 (m, 1H), 1.27 (s, 9H), 1.25 (m, 2H) Compound 97 538.0 (DMSO-d.sup.6) δ 8.08-8.03 (m, 3H), 7.66-7.59 (m, 2H), 7.15-7.11 (m, (M + H).sup.+ 2H), 3.70 (s, 2H), 2.99-2.94 (m, 3H), 1.64-1.61 (m, 9H), 1.26-1.22 (m, 1H), 1.13 (s, 9H) Compound 107 548.0 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.15-7.85 (m, 4H), 7.84-7.78 (m, (M + H).sup.+ 1H), 7.17-7.01 (m, 2H), 3.95-3.79 (m, 3H), 3.63-3.45 (m, 4H), 2.94 (s, 3H), 2.33-2.27 (m, 1H), 1.97 (t, J = 11.13 Hz, 1H), 1.72- 1.47 (m, 7H), 1.32-1.11 (m, 2H), 1.05 (d, J = 6.00 Hz, 3H) Compound 129 544.0 (DMSO-d.sup.6) δ 9.79-9.43 (m, 1H), 8.17-7.90 (m, 4H), 7.89-7.75 (m, (M + H).sup.+ 1H), 7.24-6.92 (m, 2H), 3.97-3.81 (m, 2H), 3.77-3.62 (m, 4H), 2.94 (s, 3H), 1.92-1.78 (m, 4H), 1.73-1.58 (m, 6H), 1.58-1.45 (m, 3H), 1.33-1.20 (m, 1H), 1.16-1.02 (m, 1H) Compound 134 560.1 (DMSO-d.sup.6) δ 9.69 (br s, 1H), 8.03-7.96 (m, 3H), 7.84 (br s, 1H), (M + H).sup.+ 7.73-7.69 (m, 2H), 7.14-7.12 (m, 2H), 3.87 (s, 2H), 3.05-3.03 (m, 2H), 1.64-157 (m, 6H), 1.20-1.16 (t, J = 7.2 Hz, 3H), 1.10 (s, 9H), 0.88~0.85 (m, 2H), 0.27 (br s, 4H) Compound 140 534.1 (DMSO-d.sup.6) δ 9.68-9.49 (m, 1H), 8.10-7.92 (m, 3H), 7.89-7.77 (m, (M + H).sup.+ 1H), 7.77-7.62 (m, 2H), 7.39-7.31 (m, 1H), 7.16-7.02 (m, 1H), 3.88-3.72 (m, 2H), 2.95 (d, J = 3.88 Hz, 3H), 1.83-1.33 (m, 9H), 1.13-1.09 (m, 9H), 0.88-0.74 (m, 3H) Compound 141 526.2 (DMSO-d.sup.6) δ 9.52-9.67 (m, 1H), 8.08-7.85 (m, 4H), 7.79 (s, 1H), (M + H).sup.+ 7.51-7.45 (m, 1H), 7.32-7.18 (m, 1H), 4.16-4.06 (m, 2H), 3.98- 3.80 (m, 2H), 2.93 (br s, 4H), 1.54 (br s, 11H), 1.42-1.29 (m, 3H), 1.27-1.23 (m, 3H), 1.22-0.99 (m, 2H) Compound 144 556.2 (DMSO-d.sup.6) δ 9.52-9.51 (brs, 1H), 8.03-7.97 (m, 3H), 7.83 (m, (M + H).sup.+ 1H), 7.83-7.61 (m, 2H), 7.11 (brs, 2H), 4.00 (s, 2H), 2.95 (s, 3H), 2.04-2.03 (m, 2H), 1.82 (m, 6 H), 1.15 (s, 9H) Compound 145 523.1 (DMSO-d.sup.6) δ 9.56 (s, 1H), 7.85-7.82 (m, 1H), 7.48 (s, 1H), 7.10 (M + H).sup.+ (m, 2H), 7.04-7.02 (dd, J = 8.69, 1.81 Hz, 1H), 6.91 (s, 1H), 4.09 (s, 2H), 3.77 (s, 3H), 2.93 (s, 3H), 1.68-1.62 (m, 5H), 1.59-1.49 (m, 2H), 1.31-1.25 (m, 3H), 1.16 (s, 9H) Compound 146 485.1 (CDCl.sub.3) δ 8.48-7.92 (m, 1H), 7.50-7.46 (m, 2H), 7.39-7.32 (m, (M + H).sup.+ 2H), 7.14 (s, 1H), 7.09-6.88 (m, 1H), 6.44 (s, 1H), 4.02-3.82 (br s, 2H), 2.97 (m, 1H), 2.09-2.92 (m, 3H), 2.09-2.00 (m, 2H), 1.79- 1.62 (m, 14H), 1.19-1.14 (m, 2H) Compound 147 524.1 (DMSO-d.sup.6) δ 9.61 (s, 1H), 8.35 (d, J = 1.25 Hz, 1H), 7.97-7.93 (M − H).sup.− (m, 2H), 7.65 (s, 1H), 7.14-7.04 (m, 2H), 4.21 (s, 2H), 2.95 (s, 3H), 1.74-1.52 (m, 8H), 1.34-1.26 (m, 2H), 1.14 (s, 9H) Compound 148 576.1 (DMSO-d.sup.6) δ 8.02-7.96 (m, 2H), 7.84-7.82 (m, 1H), 7.77-7.69 (m, (M + H).sup.+ 2H), 7.14-7.09 (m, 2H), 3.90 (s, 2H), 3.75-3.71 (t, J = 6.4 Hz, 2H), 3.19-3.16 (m, 2H), 1.65-1.54 (m, 6H), 1.11 (s, 9H), 1.10 (s, 1H), 0.97-0.86 (m, 2H), 0.38-0.18 (m, 4H) Compound 149 510.1 (DMSO-d.sup.6) δ 9.62 (s, 1H), 8.17 (s, 1H), 8.03-8.01 (m, 1H), 7.39 (M + H).sup.+ (d, J = 3.6 Hz, 1H), 7.21 (d, J = 3.6 Hz, 1H), 7.14 (d, J = 2.4 Hz, 1H), 7.08-7.06 (dd, J = 8.69, 2.06 Hz, 1H), 4.24 (s, 2H), 2.96 (s, 3H), 1.68-1.65 (m, 5H), 1.56-1.52 (m, 3H), 1.34-1.38 (m, 2H), 1.20 (s, 9H) Compound 151 570.1 (DMSO-d.sup.6) δ 9.58 (s, 1H), 8.06-7.0 (m, 5H), 7.13-7.11 (m, 2H), (M + H).sup.+ 3.91 (s, 2H), 3.72 (s, 4H), 2.94 (s, 3H), 1.85-1.83 (m, 4H), 1.68- 1.55 (m, 8H), 0.88-0.85 (m, 2H), 0.28-0.23 (m, 4H) Compound 153 572.1 (DMSO-d.sup.6) δ 9.59-9.57 (br s, 1H), 8.04-7.96 (m, 4H), 7.81-7.85 (M + H).sup.+ (m, 1H), 7.14 (m, 2H), 4.28-4.25 (br t, J = 7.2 Hz, 2H), 4.09 (d, J = 10.8 Hz, 2H), 3.90 (s, 2H), 3.76 (br d, J = 10.8 Hz, 2H), 2.94 (s, 3H), 2.65-2.53 (m, 2H), 1.68-1.60 (m, 6H), 0.87-0.85 (m, 2H), 0.27 (br s, 4H) Compound 155 543.1 (DMSO-d.sup.6) δ 9.66-9.57 (br s, 1H), 8.12-8.03 (m, 3H), 7.82-7.78 (M + H).sup.+ (m, 1H), 7.13-7.09 (m, 2H), 3.94-3.85 (m, 3H), 2.94 (s, 3H), 1.93- 1.83 (m, 4H), 1.66-1.57 (m, 10H), 0.88-0.85 (m, 2H), 0.27-0.22 (br s, 4H). Compound 157 483.4 (DMSO-d.sup.6) δ 9.54 (br s, 1H), 8.03-8.00 (m, 1H), 7.51-7.42 (m, (M + H).sup.+ 4H), 7.10 (m, 2H), 5.24 (d, J = 4.4 Hz, 1H), 4.37 (br dd, J = 7.50, 4.50 Hz, 1H), 3.86 (br s, 2H), 2.93 (s, 3H), 2.09-2.07 (m, 1H), 1.64-1.44 (m, 13H), 1.28-1.22 (m, 5 H) Compound 159 564.1 (DMSO-d.sup.6) δ 9.57 (br s, 1H), 8.03-7.98 (m, 3H), 7.59-7.54 (m, (M + H).sup.+ 1H), 7.12-7.07 (m, 2H), 3.89 (s, 2H), 2.93 (s, 3H), 1.69-1.61 (m, 4H), 1.14 (s, 9H), 0.88-0.85 (m, 2H), 0.27 (br s, 4H Compound 160 572.2 (DMSO-d.sup.6) δ 9.60 (br s, 1H), 8.04-7.95 (m, 3H), 7.84 (d, J = 1.2 (M + H).sup.+ Hz, 1H), 7.73-7.69 (m, 2H), 7.16-7.12 (m, 2H), 3.88 (s, 2H), 3.32 (s, 1H), 1.66-1.56 (m, 6H), 1.10 (s, 9H), 0.91-0.87 (m, 6H), 0.27 (br s, 4H) Compound 162a 570.1 (DMSO-d.sup.6) δ 9.60 (s, 1H), 8.07-7.96 (m, 2H), 7.89-7.79 (m, 1H), (M + H).sup.+ 7.73-7.70 (m, 1H), 7.66(m, 1H), 7.12-7.06 (m, 2H), 5.98-5.70 (m, 1H), 3.89 (s, 2H), 2.95 (s, 3H), 1.92-1.83 (m, 1H), 1.77-1.60 (m, 6H), 1.10-1.05 (m, 11H Compound 162b 570.1 (DMSO-d.sup.6) δ 9.68 (br s, 1H), 8.04-8.00 (m, 2H), 7.99-7.97 (m, (M + H).sup.+ 1H), 7.95-7.81 (m, 2H), 7.37 (s, 1H), 7.23-7.09 (m, 1H), 6.29-5.99 (m, 1H), 3.79 (s, 2H), 2.94 (m, 3H), 1.91-1.80 (m, 3H), 1.66-1.53 (m, 6H), 1.11 (s, 9H) Compound 163 544.2 (DMSO-d.sup.6) δ 11.57-11.53 (br s, 1H), 9.58 (s, 1H), 8.04-7.61 (m, (M + H).sup.+ 5H), 7.59-7.11 (m, 2H), 4.45 (s, 2H), 3.95 (s, 2H), 3.45-3.37 (m, 2H), 3.14-3.13 (m, 2H), 2.94 (s, 3H), 2.49-2.32 (m, 4H), 1.66 (m, 6H), 0.89-0.87 (m, 2H), 0.28 (br s, 4H) Compound 164 507.1 (DMSO-d.sup.6) δ = 9.68-9.37 (m, 1H), 8.25-8.06 (m, 3H), 7.86- (M + H).sup.+ 7.84 m, 1H), 7.66 (t, J = 7.7 Hz, 1H), 7.18-6.97 (m, 2H), 3.91- 3.80 (m, 3H), 2.94 (s, 3H), 1.89 (m, 2H), 1.77-1.51 (m, 12H), 0.96-0.87 (m, 2H), 0.27 (br s, 4H) Compound 165 509.2 (DMSO-d.sup.6) δ 9.67 (bs s, 1H), 8.24-8.00 (m, 1H), 7.48-7.42 (m, (M + H).sup.+ 4H), 7.19-7.03 (m, 2H), 5.25 (d, J = 4.8 Hz, 1H), 4.66 (m, 1H), 3.98 (s, 2H), 2.93 (s, 3H), 2.07 (m, 1H), 1.77-1.45 (m, 12H), 1.35- 1.14 (m, 2H), 0.93-0.86 (m, 2H), 0.27 (br s, 4H) Compound 165a 509.2 (DMSO-d.sup.6) δ 9.68 (br s, 1H), 8.24 (m, 1H), 7.63-7.26 (m, 4H), (M + H).sup.+ 7.29-6.80 (m, 2H), 5.25 (s, 1H), 4.47-4.43 (m, 1H), 3.96-3.83 (m, 2H), 2.93 (s, 3H), 2.12-2.05 (m, 1H), 1.78-1.36 (m, 12H), 1.31- 1.23 (m, 2H), 0.89-0.86 (m, 2H), 0.39-0.16 (m, 4H Compound 165b 509.3 (DMSO-d.sup.6) δ 9.71 (br s, 1H), 8.22-7.85 (m, 1H), 7.52-7.42 (m, (M + H).sup.+ 4H), 7.11-6.90 (m, 2H), 5.26 (d, J = 4.8 Hz, 1H), 4.38-4.35 (m, 1H), 3.96 (s, 2H), 2.93 (s, 3H), 2.11-2.07 (m, 1H), 1.65-1.45 (m, 12H), 1.35-1.18 (m, 2H), 0.89-0.86 (m, 2H), 0.44-0.07 (m, 4H) Compound 166 455.1 (DMSO-d.sup.6) δ 9.39-9.19 (brs, 1H), 7.91-7.84 (m, 3H), 7.78-7.74 (M + H).sup.+ (m, 1H), 6.67 (d, J = 2.0 Hz, 2H), 3.80 (s, 2H), 2.92 (m, 4H), 1.75- 1.59 (m, 11H), 1.53 (m, 2H), 1.37-0.98 (m, 3H) Compound 168 544.1 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.11-8.09 (m, 1H), 7.97-7.86 (m, (M + H).sup.+ 4H), 7.74-7.70 (m, 1H), 7.13 (m, 2H), 3.95 (s, 2H), 3.70-3.62 (m, 1H), 2.94 (m, 3H), 1.81-1.96 (m, 2H), 1.74-1.45 (m, 10H), 0.88- 0.85 (m, 2H), 0.13-0.36 ppm (m, 4H) Compound 170 546.1 (DMSO-d.sup.6) δ 9.56 (brs, 1 H), 7.95-7.92 (m, 2 H), 7.85 (m, 1 H), (M + H).sup.+ 7.84-7.66 (m, 2 H), 7.13 (m, 2 H), 3.88 (s, 2 H), 3.11-3.15 (m, 1 H), 2.94 (s, 3 H), 1.65-1.28 (m, 6 H), 1.22-1.28 (m, 2 H), 0.90- 0.86 (m, 5 H), 0.71-0.68 (m, 3 H), 0.27 (m, 4 H) Compound 172 556.0 (DMSO-d.sup.6) δ 9.57 (s, 1 H), 8.04-7.87 (m, 5 H), 7.70-7.79 (m, 1 (M + H).sup.+ H), 7.14-7.10 (m, 2 H), 5.57-5.54 (m, 2 H), 3.89-3.81 (m, 3 H), 2.94 (s, 3 H), 2.35-2.32 (m, 3 H), 1.99-2.15 (m, 2 H), 1.65-1.51 (m, 6 H), 0.87-0.85 (m, 2 H), 0.21-0.18 (m, 4 H) Compound 174 546.0 (DMSO-d.sup.6) δ 9.70-9.33 (br s, 1H), 9.01-8.45 (m, 1H), 8.10-7.91 (M + H).sup.+ (m, 4H), 7.64-7.83 (m, 1H), 7.14-6.97 (m, 2H), 4.36-4.58 (m, 3H), 4.13-4.33 (m, 2H), 3.73-4.00 (s, 2H), 2.94 (s, 3H), 1.81-1.49 (m, 5H), 0.99-0.79 (m, 2H), 0.39-0.05 (br s, 4H) Compound 176 558.1 (DMSO-d.sup.6) δ 9.58 (br s, 1H), 8.11-7.85 (m, 3H), 7.80-7.78 (m, (M + H).sup.+ 1H), 7.75-7.71 (m, 2H), 7.10-7.18 (m, 1H), 3.98 (br s, 2H), 3.39- 3.57 (m, 1H), 2.94 (s, 3H), 1.77-1.53 (m, 10H), 1.44-1.18 (m, 4H), 0.88-0.85 (m, 2H), 0.27-0.14 (m, 4H) Compound 178 574.1 (DMSO-d.sup.6) δ 9.57 (s, 1 H) 8.06-7.97 (m, 4 H), 7.79-7.94 (m, 1 (M + H).sup.+ H), 7.74-7.72 (m, 1 H), 7.13 (m, 2 H), 3.86 (s, 2 H), 3.64-3.73 (m, 4 H), 2.94 (s, 3 H), 2.06-2.16 (m, 1 H), 1.73-1.58 (m, 7 H) 1.19 (s, 3 H), 0.77-1.00 (m, 2 H) 0.27 (s, 4 H) Compound 180 572.1 (DMSO-d.sup.6) δ 9.57 (s, 1 H), 7.99-7.78 (m, 5 H), 7.73-7.69 (m, 1 (M + H).sup.+ H), 7.13 (m, 2 H), 3.87 (br s, 2 H), 2.94 (s, 3 H), 1.64-1.54 (m, 10 H), 1.48-1.49 (m, 1 H), 0 1.24-1.09 (m, 6 H), 0.86 (m, 2 H), 0.26- 0.23 (m, 4 H) Compound 182 558.1 (DMSO-d.sup.6) δ 9.58 (s, 1H), 8.13-8.00 (m, 4H), 7.97-7.95 (m, 1H), (M + H).sup.+ 7.84 (m, 1H), 7.14-6.99 (m, 2H), 3.89 (s, 2H), 2.95 (s, 3H), 2.08 (m, 2H), 1.65-1.62 (m, 10H), 1.28 (s, 3H), 0.88-0.85 (m, 2H), 0.15-0.36 (m, 4H) Compound 184 572.1 (DMSO-d.sup.6) δ 9.59 (br s, 1 H), 8.09-7.93 (m, 3 H), 7.86 (m, 1 H), (M + H).sup.+ 7.74-7.70 (m, 1 H), 7.65 (d, J = 8.0 Hz, 1 H), 7.14-7.11 (m, 2 H), 3.88 (br s, 2 H), 3.08 (m, 1 H), 2.95 (s, 3 H), 2.21-2.09 (m, 1 H), 1.75-1.56 (m, 11H), 1.47-1.33 (m, 1 H), 0.88-0.85 (m, 2 H), 0.78 (d, J = 6.4 Hz, 3 H), 0.26 (m, 4 H) Compound 186 558.1 (DMSO-d.sup.6) δ 9.59 (br s, 1 H), 8.11-7.94 (m, 3 H), 7.87 (d, J = 8.0 (M + H).sup.+ Hz, 2 H), 7.74-7.70 (m, 1 H), 7.13 (m, 2 H), 3.88 (s, 2 H), 2.95 (s, 3 H), 2.71-2.59 (m, 1 H), 1.76-1.48 (m, 6 H), 1.00 (d, J = 6.4 Hz, 3 H), 0.89-0.85 (m, 2 H), 0.72 (m, 1 H), 0.21-0.39 (m, 5 H), 0.05- 0.20 (m, 2H), 0.11 (m, 1 H) Compound 188 574.1 (DMSO-d.sup.6) δ 9.59 (br s, 1 H), 8.63 (m, 1 H), 7.95-7.94 (m, 4 H), (M + H).sup.+ 7.76-7.72 (m, 1 H), 7.15-7.14 (m, 2 H), 4.29 (s, 1 H), 4.05 (s, 2 H), 3.89 (s, 2H), 2.95 (s, 3 H), 1.72-1.57 (m, 6 H), 1.19 (s, 3 H), 1.11 (s, 3 H), 0.89-0.87 (m, 2 H), 0.33-0.18 (br s, 4 H) Compound 190 556.1 (CDCl.sub.3) 8.33 (m, 1H), 8.15 (m, 1H), 7.81-7.79 (m, 1H), 7.70-7.66 (M + H).sup.+ (t, J = 7.2 Hz, 1H), 7.21 (m, 1H), 7.05-7.10 (m, 1H), 6.62 (s, 1H), 4.83 (s, 2H), 4.82-4.77 (m, 1H), 3.93-3.88 (br s, 2H), 3.02 (s, 3H), 2.96-2.91 (m, 2H).2.60-2.55 (m, 2H), 1.82-1.80 (m, 3H), 1.71- 1.68 (m, 3H), 0.97-0.92 (m, 2H), 0.33 (s, 4H) Compound 192 580.1 (DMSO-d.sup.6) δ 9.54 (br s, 1 H), 8.42-7.93 (m, 4 H), 7.78-7.75 (m, 1 (M + H).sup.+ H), 7.14-6.96 (m, 2 H), 3.96 (s, 2 H), 3.58-3.71 (m, 1 H), 2.95 (s, 3 H), 2.74-2.42 (m, 2 H), 2.46-2.34 (m, 2 H), 1.82-1.61 (m, 6 H), 0.95-0.87 (m, 2 H), 0.37 (m, 4 H) Compound 194 574.2 (MeOD) 8.19-8.00 (m, 3 H), 7.82 (m, 1 H), 7.74-7.70 (m, 2 H), (M − H).sup.− 7.21-7.08 (m, 2 H), 3.95 (br s, 1H), 3.71-3.65 (m, 1 H) 2.94 (s, 3H) 1.84 (m, 2 H) 1.70 (m, 4 H) 1.14-1.11 (m, 8 H) 095-0.89 (m, 3 H) 0.32 (s, 4 H). Compound 196 570.1 (DMSO-d.sup.6) δ 9.59 (br s, 1 H), 8.10-7.94 (m, 4 H), 7.87 (m, 1 H), (M + H).sup.+ 7.76-7.72 (m, 1 H), 7.14-7.15 (m, 2 H), 5.71-5.68 (m, 1 H), 5.25- 5.22 (m, 1 H), 3.90 (br s, 2 H), 3.71 (br s, 1 H), 2.95 (s, 3 H), 1.87 (m, 2 H), 1.67-1.57 (m, 8 H), 1.39 (m, 2 H), 0.88-0.85 (d, J = 9.6 Hz, 2 H), 0.28-0.26 (m, 4 H) Compound 198 560.1 (DMSO-d.sup.6) δ 9.59 (br s, 1 H), 8.11-7.90 (m, 3 H), 7.85 (m, 1 H), (M + H).sup.+ 7.74-7.64 (m, 2 H), 7.14-7.13 (m, 2 H), 3.88 (br s, 2 H), 2.98 (m, 1 H), 2.95 (s, 3 H), 1.74-1.66 (m, 6 H), 1.36-1.28 (m, 2 H), 1.26- 1.23 (m, 2 H), 0.85-0.80 (m, 2 H), 0.67-0.65 (m, 6 H), 0.28-0.26 (m, 4H) Compound 200 562.1 (DMSO-d.sup.6) δ 9.59 (br s, 1 H), 8.11-7.95 (m, 3 H), 7.85-7.83 (m, 2 (M + H).sup.+ H), 7.77-7.70 (m, 1 H), 7.14 (m, 2 H), 3.90 (s, 2 H), 3.17-3.16 (m, 1 H), 3.12 (m, 1 H), 3.10 (s, 3 H), 2.95 (s, 3 H), 1.67-1.66 (m, 6 H), 0.92-0.86 (m, 5 H), 0.27 (m, 4 H) Compound 202 560.1 (DMSO-d.sup.6) δ 8.12-8.11(m, 1H), 8.07-8.05 (m, 1H), 7.79 (br d, J = (M + H).sup.+ 7.2 Hz, 1H), 7.68-7.64 (m, 1H), 7.18 (s, 1H), 6.37 (s, 1H), 5.49 (s, 1H), 3.92-3.86 (m, 2H), 3.40 (s, 2H), 3.00 (s, 3H), 1.83-1.80 (m, 2H), 1.71-1.58 (m, 4H), 0.95-0.92 (m, 2H), 0.88-0.85 (m, 2H) 0.70-0.67 (m, 2H) 0.32 (br s, 4H) Compound 204 562.2 (DMSO-d.sup.6) δ 9.58 (br s, 1 H), 8.18-8.16 (br d, J = 7.6 Hz, 1 H), (M + H).sup.+ 7.96-7.92 (m, 4 H), 7.76-7.72 (t, J = 8.0 Hz, 1 H), 7.14-7.08 (m, 2 H), 4.73-4.54 (m, 1 H), 3.88 (br s, 2 H), 3.23-3.27 (m, 1 H), 2.94 (s, 3 H), 2.45-2.41 (m, 2 H) 1.95-1.96 (m, 2 H) 1.79-1.50 (m, 6 H), 0.88-0.86 (m, 2 H) 0.275 (br s, 4 H) Compound 206 560.1 (DMSO-d.sup.6) δ 9.58-9.41 (br s, 1 H) 8.58-8.53 (br s, 1 H), 8.19-7.89 (M + H).sup.+ (m, 4 H), 7.76-7.72 (m, 1 H), 7.13 (m, 2 H), 4.55 (d, J = 6.0 Hz, 2 H), 4.13 (d, J = 6.0 Hz, 2 H), 3.88 (br s, 2 H) 2.94 (s, 3 H) 1.66- 1.57 (m, 6 H), 1.41 (s, 3 H), 0.88-0.75 (m, 2 H) 0.27 (br s, 4 H) Compound 208 562.1 (DMSO-d.sup.6) δ 9.61 (br.s, 1 H), 8.11-7.93 (m, 3 H), 7.86 (m, 1 H), (M + H).sup.+ 7.73-7.65 (m, 2 H), 7.13-7.09 (m, 2 H), 4.60-4.70 (t, J = 4.8 Hz, 1 H), 3.87 (br s, 2 H), 3.29-3.27 (m, 1 H), 3.18-3.15 (m, 1 H), 2.96 (m, 1 H), 2.94 (s, 3H), 1.65-1.51 (m, 7 H), 1.12-1.29 (m, 1 H), 0.98-0.86 (m, 2 H), 0.69-0.59 (m, 3 H), 0.27 (br s, 4 H) Compound 210 560.1 (DMSO-d.sup.6) δ 9.58 (br s, 1 H), 7.99 (s, 1 H), 7.95 (d, J = 7.8 Hz, 1 (M + H).sup.+ H), 7.86 (br d, J = 5.9 Hz, 1 H), 7.73 (t, J = 24.0 Hz, 1 H), 7.61 (d, J = 8.3 Hz, 1 H), 7.03-7.18 (m, 2 H), 3.88 (s, 2 H), 2.98-3.07 (m, 1 H), 2.95 (s, 3 H), 1.50-1.72 (m, 7 H), 0.87 (br d, J = 11.9 Hz, 2 H), 0.74-0.81 (m, 9 H), 0.21-0.34 (m, 4 H) Compound 212 530.2 (DMSO-d.sup.6) δ 9.58-9.53 (m, 1 H), 8.07-8.04 (s, 1 H), 8.01-7.97 (M + H).sup.+ (m, 3 H), 7.78-7.74 (m, 1 H), 7.14-7.08 (m, 2 H), 3.98 (br s, 2 H), 2.94 (s, 3 H), 2.16-2.10 (m, 1 H), 1.77-1.52 (m, 6 H), 0.92-0.87 (m, 2 H), 0.42-0.55 (m, 2 H), 0.34-0.41 (m, 2 H), 0.27 (br s, 4 H) Compound 214 574.1 (DMSO-d.sup.6) δ 9.69-9.43 (br s, 1 H), 8.15-7.94 (m, 3 H), 7.84-7.79 (M + H).sup.+ (m, 2 H), 7.71-7.67 (m, 1 H), 7.14 (m, 1 H), 4.61 (br s, 1 H), 3.89 (br s, 2 H), 3.38-3.52 (m, 2 H), 2.94 (s, 3 H), 2.58-2.63 (m, 1 H), 1.66 (m, 6 H), 0.87-0.81 (m, 3 H), 0.27 (br s, 6 H), 0.15-0.09 (m, 2 H). Compound 216 544.1 (DMSO-d.sup.6) δ 9.58 (br.s, 1 H), 8.20 (s, 1 H), 8.05-7.87 (m, 3 H), (M + H).sup.+ 7.76-7.72 (m, 1 H), 7.13-7.09 (m, 1 H), 7.10 (s, 1H), 3.88 (s, 2 H), 2.94 (s, 3 H), 1.46-1.76 (m, 6 H), 1.07 (s, 3 H), 0.89-0.86 (m, 2 H), 0.63-0.60 (m, 2 H), 0.41-0.38 (m, 2 H), 0.27 (br s, 4 H) Compound 218 560.1 (DMSO-d.sup.6) δ 9.58 (s, 1 H), 8.09-7.90 (m, 4 H), 7.66-7.80 (m, 1 (M + H).sup.+ H), 7.14-7.10 (m, 1 H), 7.15 (s, 1 H), 5.00-4.91 (m, 1 H), 3.89- 3.62 (m, 3 H), 3.25-3.07 (m, 1 H), 2.95 (s, 3 H), 2.06 (m, 1 H), 1.83-2.01 (m, 2 H), 1.66-1.51 (m, 7 H), 0.96-0.87 (m, 2 H), 0.22 (br s, 4 H) Compound 220 562.1 (DMSO-d.sup.6) δ 9.60 (br s, 1 H), 8.09-7.91 (m, 3 H), 7.84 (m, 1 H), (M + H).sup.+ 7.75-7.62 (m, 1 H), 7.51 (s, 1 H), 7.13-7.09 (m, 2 H), 4.79 (t, J = 6.0 Hz, 1 H), 3.89 (s, 2 H), 3.21 (d, J = 5.6 Hz, 2 H), 2.94 (s, 3 H), 1.74-1.50 (m, 6 H), 0.96-1.08 (m, 6 H), 0.93-0.80 (m, 2 H), 0.27 (brs, 4 H) Compound 222 574.1 (DMSO-d.sup.6) δ 9.58 (br. s, 1 H), 8.07-7.95 (m, 2 H), 7.94-7.88 (M + H).sup.+ (m, 3 H), 7.75-7.71 (m, 1H) 7.14-7.11 (m, 1 H), 3.88-3.80 (br s, 2 H), 3.41-3.32 (m, 1 H), 3.00 (s, 3 H), 2.90 (s, 3 H), 2.27-2.25 (m, 2 H), 2.04-1.88 (m, 1 H), 1.66-1.56 (m, 8 H), 0.89-0.86 (d, J = 10.4 Hz, 2 H), 0.27 (br s, 4 H) Compound 223 556.1 (DMSO-d.sup.6) δ 9.57 (brs, 1H), 8.71 (s, 1H), 7.99-7.88 (m, 4H), (M + H).sup.+ 7.74-7.72 (m, 1H), 7.13-7.07 (m, 2H), 3.89 (s, 2H), 2.94 (s, 3H), 2.28 (s, 1H), 1.71-1.65 (m, 12H), 0.88-0.85 (m, 2H), 0.26 (br d, J = 6.50 Hz, 3H) Compound 224 594.2 (CDCl.sub.3) δ 8.02-8.15 (m, 3 H), 7.79 (br d, J = 7.13 Hz, 1 H), 7.65- (M + H).sup.+ 7.69 (m, 1 H), 7.20 (s, 1 H), 7.00-7.09 (m, 1 H), 6.45 (s, 1 H), 5.08 (br s, 1 H) 3.88-3.95 (m, 2 H), 3.00 (s, 3 H) 2.84-2.98 (m, 2 H) 2.55-2.63 (m, 2 H) 1.68-1.96 (m, 6 H), 1.49 (s, 3 H), 0.91- 0.94 (m, 2 H), 0.32 (br s, 4 H) Compound 225 556.1 (DMSO-d.sup.6) δ 9.56 (brs, 1H), 8.07-7.93 (m, 5H), 7.77 (d, J = 7.6, (M + H).sup.+ 1H), 7.14-7.04 (m, 2H), 3.90 (br s, 2H), 3.26-3.30 (m, 2H), 2.94 (s, 3H), 1.76-152 (m, 6H), 0.99-1.10 (m, 1H), 0.88 (br d, J = 10.9 Hz, 2H), 0.77-0.82 (m, 1H), 0.65-0.76 (m, 4H), 0.27 (br s, 4H) Compound 226 576.1 (DMSO-d.sup.6) δ 9.57 (s, 1 H) 8.38-8.48 (s, 1 H) 7.94-8.10 (m, 2 (M + H).sup.+ H) 7.83-7.93 (m, 1 H) 7.70-7.80 (m, 1 H) 7.01-7.19 (m, 2 H) 3.80-3.96 (s, 2 H) 3.48-3.60 (m, 2 H) 2.88-3.00 (s, 3 H) 2.68- 2.74 (m, 2 H) 2.11-2.22 (m, 1 H) 1.85-1.95 (m, 1 H) 1.46-1.78 (m, 9 H) 1.35-1.43 (m, 1 H) 1.12-1.30 (m, 1 H) 0.80-0.95 (m, 2 H) 0.18-0.34 (br s, 4 H) Compound 227 574.1 (DMSO-d.sup.6) δ 7.99-7.91 (m, 2 H), 7.83 (br d, J = 7.70 Hz, 2H), (M + H).sup.+ 7.75-7.66 (m, 2H), 7.19 (d, J = 1.83 Hz, 1 H), 7.07 (br d, J = 8.19 Hz, 1 H), 3.90 (s, 2 H), 3.78 (t, J = 6.60 Hz, 4 H), 3.05 (s, 2 H), 1.97- 1.93 (m, 2 H), 1.69-1.48 (m, 10 H), 0.96 (br d, J = 13.20 Hz, 2 H), 0.54-0.09 (m, 4 H) Compound 228 600.1 (DMSO-d.sup.6) δ 8.04-7.94 (m, 4H), 7.84-7.80 (m, 1H), 7.14-7.10 (m, (M + H).sup.+ 2H), 3.91 (ms, 2H), 3.78-3.72 (m, 6H), 3.24-3.18 (m, 2H), 1.87- 1.83 (m, 4 H), 1.68-1.55 (m, 8H), 0.87-0.83 (m, 2H), 0.28-0.23 (m, 4H) Compound 229 573.1 (DMSO-d.sup.6) δ 9.52-9.65 (m, 1 H), 7.94-8.16 (m, 4 H), 7.76-7.86 (M + H).sup.+ (m, 1 H), 7.04-7.18 (m, 2 H), 4.95 (m, 1 H), 3.81-3.95 (m, 3 H), 3.73 (br t, J = 6.32 Hz, 2 H), 3.18 (br t, J = 6.44 Hz, 2 H), 1.77-1.92 (m, 4 H), 1.50-1.72 (m, 10 H), 0.88 (br d, J = 9.26 Hz, 2 H), 0.28 (br s, 4 H) Compound 230 610.1 (DMSO-d.sup.6) δ 8.51-8.22 (m, 1 H), 8.22-7.84 (m, 4 H), 7.82- (M + H).sup.+ 7.68 (m, 1 H), 7.24-6.96 (m, 2 H), 3.97-3.81 (m, 2 H), 3.79- 3.70 (m, 2 H), 3.68-3.59 (m, 1 H), 3.23-3.13 (m, 2 H), 2.80- 2.64 (m, 2 H), 2.38-2.29 (m, 2 H), 1.78-1.46 (m, 6 H), 0.97- 0.77 (m, 2 H), 0.37-0.12 (m, 4 H) Compound 231 534.2 (DMSO-d.sup.6) δ 9.58 (s, 1 H) 8.36 (s, 1 H) 7.81-7.91 (m, 2 H) 7.01- (M + H).sup.+ 7.15 (m, 2 H) 4.02 (s, 2 H) 2.94 (s, 3 H) 1.52-1.67 (m, 7 H) 1.22- 1.30 (m, 3 H) 1.19 (s, 9 H) Compound 233 558.1 (DMSO-d.sup.6) δ 9.57 (s, 1H), 8.27-8.44 (m, 1H), 7.71-8.12 (m, 4H), (M + H).sup.+ 7.64-7.80 (m, 1H), 6.92-7.23(m, 2H), 4.69 (br d, J = 1.6 Hz, 1H), 4.55 (br s, 1H), 4.23-4.39 (m, 1H), 3.77-4.00(m, 2H), 2.95 (s, 3H), 2.17-2.34 (m, 2H), 1.84-2.02 (m, 1H), 1.46-1.75 (m, 7H), 0.76- 0.98 (m, 2H), 0.15-0.38 (m, 4H) Compound 235 570.1 (DMSO-d.sup.6) δ 8.09 (br s, 1H), 8.04 (d, J = 7.88 Hz, 1H), 7.79 (br d, (M + H).sup.+ J = 7.63 Hz, 1H), 7.71-7.63 (m, 1H), 7.21 (s, 2H), 6.28 (br s, 1H), 5.67 (ddt, J = 9.82, 3.60, 1.67, 1.67 Hz, 1H), 5.56-5.48 (m, 1H), 4.59 (d, J = 8.25 Hz, 1H), 4.03-3.78 (m, 2H), 3.65-3.50 (m, 1H), 3.00 (s, 3H), 2.32-2.20 (m, 1H), 2.09 (br d, J = 2.38 Hz, 2H), 1.93- 1.63 (m, 8H), 1.26 (s, 1H), 1.02-0.77 (m, 3H), 0.32 (br s, 4H) Compound 237 592.1 (DMSO-d.sup.6) δ 8.15-8.65 (br s, 1H), 7.95-8.00 (m, 2H), 7.83 (d, J = (M + H).sup.+ 8.0 Hz 3H), 7.66-7.70 (m, 1H), 7.20 (s, 1H), 7.00 (m, 1H), 6.27 (s, 1H), 3.88-3.90 (m, 2H), 3.67 (s , 4H), 3.00 (s, 3H), 2.29 (d, J = 11.6 Hz, 2H), 1.80-1.82 (m, 3H), 1.71 (m, 3H), 0.92-0.4 (m, 2H), 3.19 (s, 4H) (R)-Compound 239 562.1 (DMSO-d.sup.6) δ 8.15-8.30 (br s, 1H), 7.98-8.02 (m, 2H), 7.83 (d, J = (M + H).sup.+ 7.2 Hz, 1H), 7.67-7.71 (m, 1H), 7.19 (s, 1H), 7.10 (m, 1H), 6.45 (s, 1H), 5.10-5.23 (d, J = 53.2 Hz, 2H), 3.89 (m, 2H), 3.59-3.63 (m, 3H), 3.31-3.32 (m, 1H), 2.15-2.25 (m, 1H), 1.98 (m, 2H), 1.71 (m, 2H), 0.91-0.93 (m, 2H), 0.31 (s , 4H) (S)-Compound 239 562.1 (CDCl.sub.3) δ 8.12-8.34 (m, 1H), 7.97-8.09 (m, 2H), 7.81-7.88 (m, (M + H).sup.+ 1H), 7.67-7.74 (m, 1H), 7.18-7.25 (m, 1H), 6.96-7.15 (m, 1H), 6.25-6.40 (m, 1H), 5.01-5.35 (m, 1H), 3.75-4.17 (m, 2H), 3.59- 3.66 (m, 2H), 3.47-3.58 (m, 1H), 3.28-3.39 (m, 1H), 2.98-3.04 (m, 3H), 2.16-2.27 (m, 1H), 1.97 (br s, 1H), 1.86-1.95 (m, 1H), 1.77- 1.85 (m, 2H), 1.65-1.76 (m, 3H), 0.88-1.00 (m, 2H), 0.24-0.42 (br s, 4H Compound 240 532.1 (DMSO-d.sup.6) δ 9.59 (s, 1 H) 7.83-8.11 (m, 3 H) 7.75-7.82 (m, 1 (M + H).sup.+ H) 6.91-7.21 (m, 2 H) 3.76-4.00 (s, 2 H) 2.79-3.06 (m, 7 H) 1.61-1.43(m, 13 H) 1.03-1.30 (m, 4 H) Compound 241 518.1 (DMSO-d.sup.6) δ 9.59 (1 H, br s) ) 7.81-8.40 (m, 4 H) 7.72-7.80 (M + H).sup.+ (m, 1 H) 6.78-7.25 (m, 2 H) 3.85 (s, 2 H) 3.19 (br s, 4 H) 2.80- 3.03 (m, 3 H) 1.41-1.90 (m, 11 H) 0.93-1.38 (m, 3 H) Compound 243 504.0 (DMSO-d.sup.6) δ 9.61 (s, 1H), 8.00 (s, 1H), 7.95 (d, J = 7.9 Hz, 1H), (M + H).sup.+ 7.82 (d, J = 7.4 Hz, 1H), 7.72-7.66 (m, 1H), 7.65 (s, 1H), 7.16 (d, J = 2.0 Hz, 2H), 5.72 (s, 2H), 3.93 (s, 2H), 2.94 (s, 3H), 2.60 (s, 4H), 1.09 (s, 9H) Compound 245 558.2 (DMSO-d.sup.6) δ 9.49-9.56 (m, 1 H), 7.91-7.98 (m, 3 H), 7.73-7.74 (M + H).sup.+ (m, 1 H), 6.99-7.12 (m, 2 H), 3.88-3.90 (br s, 2 H), 3.65-3.80 (m, 2 H), 2.91 (s, 3 H), 1.93-2.08 (m, 2 H), 1.56-1.75 (m, 6 H), 1.33 (s, 6 H), 0.85-0.90 (m, 2 H), 0.18-0.35 (m, 4 H) Compound 247 562.1 (DMSO-d.sup.6) δ 8.12-8.34 (m, 1H), 7.97-8.09 (m, 2H), 7.81-7.88 (m, (M + H).sup.+ 1H), 7.67-7.74 (m, 1H), 7.18-7.25 (m, 1H), 6.96-7.15 (m, 1H), 6.25-6.40 (m, 1H), 5.01-5.35 (m, 1H), 3.75-4.17 (m, 2H), 3.59- 3.66 (m, 2H), 3.47-3.58 (m, 1H), 3.28-3.39 (m, 1H), 2.98-3.04 (m, 3H), 2.16-2.27 (m, 1H), 1.97 (br s, 1H), 1.86-1.95 (m, 1H), 1.77- 1.85 (m, 2H), 1.65-1.76 (m, 3H), 0.88-1.00 (m, 2H), 0.24-0.42 (br s, 4H) Compound 249 558.1 (DMSO-d.sup.6) δ 9.58 (s, 1 H) 7.87-8.18 (m, 4 H) 7.75-7.82 (m, 1 (M + H).sup.+ H) 7.14 (d, J = 2.00 Hz, 2 H) 3.90 (br s, 2 H) 3.41 (dd, J = 9.82, 7.19 Hz, 1 H) 3.30 (br s, 1 H) 3.16-3.26 (m, 1 H) 2.95 (s, 3 H) 2.72 (dd, J = 9.88, 7.50 Hz, 1 H) 1.99-2.09 (m, 1 H) 1.87 (td, J = 11.73, 6.69 Hz, 1 H) 1.46-1.76 (m, 6 H) 1.23-1.35 (m, 1 H) 0.88 (br d, J = 11.76 Hz, 2 H) 0.80 (d, J = 6.63 Hz, 3 H) 0.28 (br d, J = 5.63 Hz, 4 H) Compound 250 517.1 (DMSO-d.sup.6) δ 8.22-7.93 (m, 3H), 7.91 (m, 1H), 7.86-7.74 (m, (M + H).sup.+ 3H), 3.96 (s, 2H), 3.40 (s , 4H), 2.99-2.82 (m, 4H), 1.76-1.60 (m, 6H), 1.54 (s, 5H), 1.38 (d, J = 4.0 Hz, 2H), 1.33-1.09 (m, 3H) Compound 252 520.1 (DMSO-d.sup.6) δ 9.57 (br s, 1 H), 7.92-8.04 (m, 2 H), 7.82 (br d, (M + H).sup.+ J = 6.85 Hz, 1 H), 7.63-7.74 (m, 2 H), 7.01-7.16 (m, 2 H), 3.77- 3.91 (m, 2 H), 2.94 (s, 3 H), 1.85-1.99 (m, 2 H), 1.62-1.84 (m, 2 H), 1.30-1.42 (m, 2 H), 1.20-1.27 (m, 2 H), 1.11 (s, 9 H), 0.92- 1.04 (m, 3 H), 0.81-0.90 (m, 1 H). Compound 254 556.1 (DMSO-d.sup.6) δ 9.54-9.63 (br s, 1 H), 7.89-8.11 (m, 3 H), 7.75- (M + H).sup.+ 7.83 (m, 1 H), 7.04-7.18 (m, 2 H), 3.86-3.97 (s, 2 H), 3.42 (br d, J = 9.26 Hz, 2 H), 3.11-3.21 (s, 2 H), 2.90-2.98 (s, 3 H), 1.57- 1.74 (m, 6 H), 1.45-1.54 (m, 2 H), 0.81-0.96 (m, 2 H), 0.46- 0.56 (m, 1 H), 0.19-0.37 (m, 4 H), −0.24-0.14 (m, 1 H). Compound 255 560.1 (DMSO-d.sup.6) δ 9.54-9.63 (s, 1 H), 7.93-8.12 (m, 4 H), 7.79-7.88 (M + H).sup.+ (m, 1 H), 7.13 (s, 2 H), 5.64 (s, 1 H), 3.92 (br s, 2 H), 3.50-3.66 (m, 4 H), 2.94 (s, 3 H), 1.68 (s, 6 H), 1.16 (s, 3 H), 0.80-0.95 (m, 2 H), 0.27 (br s, 4 H). Compound 257 566.0 (DMSO-d.sup.6) δ 9.57 (br s, 1 H) 8.13-8.02 (m, 3 H) 7.83 (t, J = (M + H).sup.+ 7.60, 1 H) 7.11 (d, J = 1.60 Hz, 2 H) 4.32 (t, J = 12.80 Hz, 4 H) 3.83- 3.82 (m, 2 H) 2.92 (s, 3 H) 1.67-1.61 (m, 6 H) 0.84-0.80 (m, 2 H) 0.26-0.22 (m, 4 H) Compound 258 542.1 (DMSO-d.sup.6) δ 9.58 (br s, 1 H), 8.20-7.94 (m, 4 H), 7.89-7.81 (m, (M + H).sup.+ 1 H), 7.14 (s, 2 H), 4.95 (s, 2H), 4.41 (br s, 4 H), 4.00-3.82 (m, 2H), 2.94 (s, 3 H), 1.77-1.49(m, 6H), 0.97-0.80(m, 2 H), 0.38-0.19 (m, 4H) Compound 260 544.1 (DMSO-d.sup.6) δ 9.57 (br s , 1 H), 8.14-7.91 (m, 4 H), 7.86-7.82 (M + H).sup.+ (m, 1 H), 7.13 (J = 2.0 Hz, br d, 2 H), 3.92-3.86 (m, 4 H), 3.29- 3.26 (m, 2 H), 2.94 (s, 3 H), 2.52-2.51 (m, 1 H), 1.68 (br s , 6 H), 0.86 (J = 6.8 Hz, br d, 5 H), 0.27-0.24 (m, 4 H) Compound 261 558.7 (DMSO-d.sup.6) δ 9.43-9.95 (br s, 1H), 8.08-8.18 (m, 1H), 7.81- (M + H).sup.+ 8.00 (m, 3H), 7.66-7.78 (m, 1H), 7.05-7.20 (m, 2H), 3.81-3.95 (s, 2H), 3.57-3.75 (m, 1H), 3.00-3.11 (m, 2H), 1.83-1.94 (m, 2H), 1.43-1.76 (m, 10H), 1.15-1.22 (m, 3H), 0.82-0.91 (m, 2H), 0.19-0.33 (m, 4H) Compound 262 552.1 (DMSO-d.sup.6) δ 9.54-9.74 (br s, 1 H) 8.40 (s, 1 H) 7.69-8.19 (m, 3 (M + H).sup.+ H) 6.94-7.24 (m, 2 H) 4.06 (s, 2 H) 2.89 (s, 3 H) 1.69-1.76 (m, 6 H) 1.19 (s, 9 H) 0.89-0.90 (m, 2 H) 0.24 (s, 4 H) Compound 264 555.1 (DMSO-d.sup.6) δ 9.57 (br s, 1 H) 9.28 (br s, 1 H) 8.03-7.97 (m, 4 H) (M + H).sup.+ 7.82-7.78 (m, 1 H) 7.14-7.12 (m, 2 H) 3.91 (br s, 2 H) 2.95 (s, 3 H) 1.65 (br s, 6 H) 1.44-1.35 (m, 4 H) 0.83 (br s, 2 H) 0.25 (br s, 4H) Compound 266 559.2 (CD.sub.3OD) δ 9.60 (brs, 1 H) 7.94-8.03 (m, 2 H) 7.83 (m, 1 H) 7.69- (M + H).sup.+ 7.73 (m, 1 H) 7.57 (m, 1 H) 6.98-7.23 (m, 2 H) 3.88 (s, 2 H) 2.94 (s, 3 H) 1.57-1.65 (m, 6 H) 1.36-1.50 (m, 2 H) 1.04 (s, H) 0.85-0.88 (m, 2 H) 0.71-0.74 (m, 3 H) 0.27 (m, 4 H) Compound 268 552.1 (DMSO-d.sup.6) δ 9.60 (br s, 1H), 8.36 (s, 1H), 7.87-8.14 (m, 2H), (M + H).sup.+ 7.55-7.80 (m, 1H), 7.01-7.27 (m, 2H), 4.27 (s, 2H), 2.96 (s, 3H), 1.62-1.92 (m, 6H), 1.17 (s, 9H), 0.86-1.02 (m, 2H), 0.31 ppm (br s, 4H) Compound 269 566.1 (DMSO-d.sup.6) δ 9.69 (br s, 1H), 8.35 (s, 1H), 7.96 (m, 2H), 7.65 (s, (M + H).sup.+ 1H), 7.01-7.24 (m, 2H), 4.19-4.38 (m, 2H), 3.05 (q, 2H), 1.62-1.89 (m, 6H), 1.07-1.29 (m, 12H), 0.92 (br d, J = 13.0 Hz, 2H), 0.31 (br s, 4H) Compound 270 527.1 (DMSO-d.sup.6) δ 9.64-9.54 (m, 1H), 8.20-8.00 (m, 1H), 7.92-7.80 (M + H).sup.+ (m, 2H), 7.78-7.66 (m, 2H), 7.19-7.07 (m, 2H), 3.99-3.79 (s, 2H), 2.97-2.91 (s, 3H), 1.94-1.75 (m, 4H), 1.72-1.64 (m, 4H), 1.61-1.49 (m, 6H), 1.44-1.36 (m, 1H), 0.92-0.83 (m, 2H), 0.32- 0.21 (m, 4H) Compound 272 600.0 (DMSO-d.sup.6) δ 9.81-9.58 (m, 1 H), 8.57 (s, 1 H), 8.11-7.82 (m, 2 (M + H).sup.+ H), 7.24-7.01 (m, 2 H), 4.58-4.31 (s, 2 H), 3.86-3.71 (m, 6 H), 3.14-2.99 (m, 2 H), 2.16-1.99 (m, 2H), 1.96-1.84 (m, 8 H), 1.67-1.61 (m, 2H), 1.30-1.13 (m, 3 H) Compound 274 582.1 (DMSO-d.sup.6) δ 9.58 (br s, 1 H) 8.38 (s, 1 H) 8.08-7.94 (m, 1 H) (M + H).sup.+ 7.93-7.80 (m, 2 H) 7.18-7.01 (m, 2 H) 4.93 (br d, J = 2.00 Hz, 1 H) 4.07 (s, 2 H) 3.73 (br d, J = 2.00 Hz, 2 H) 3.19 (t, J = 6.75 Hz , 2 H) 1.78-1.58 (m, 6 H) 1.20 (s, 9 H) 0.89 (br d, J = 10.51 Hz, 2 H) 0.29 (s, 4 H) Compound 275 566.1 (DMSO-d.sup.6) δ 9.66 (br s, 1 H), 8.37 (s, 1 H), 8.07 (m, 1 H), 7.92- (M + H).sup.+ 7.82 (m, 2 H), 7.13 (d, J = 1.97 Hz, 2 H), 4.06 (s, 2 H), 3.03 (m, 2 H), 1.80-1.58 (m, 6 H), 1.21-1.15 (m, 12 H), 0.88 (br d, J = 10.74 Hz, 2 H), 0.29 (s, 4 H) Compound 277 562.0 (DMSO-d.sup.6) δ 9.59 (s, 1H), 8.41 (s, 1H), 8.19-7.95 (m, 1H), 7.93- (M + H).sup.+ 7.82 (m, 2H), 7.18-7.01 (m, 2H), 4.18 (s, 2H), 2.96 (s, 3H), 2.14- 1.73 (m, 8H), 1.20 (s, 9H) Compound 279 576.1 (DMSO-d.sup.6) δ 9.58 (br s, 1 H), 8.56 (s, 1 H), 8.03 (br s, 2 H), 7.18- (M + H).sup.+ 7.04 (m, 2 H), 4.07 (s, 2 H), 3.82 (s, 4 H), 2.95 (s, 3 H), 1.99- 1.89 (m, 4 H), 1.68 (br s, 8 H), 0.88 (br d, J = 5.63 Hz, 2 H), 0.36- 0.21 (m, 4 H) Compound 281 600.0 (DMSO-d.sup.6) δ 9.67-9.49 (m, 1H), 8.65-8.52 (m, 1H), 8.14-7.91 (M + H).sup.+ (m, 2H), 7.21-7.01 (m, 2H), 4.20-4.05 (m, 2H), 3.22-3.11 (m, 4H), 2.96-2.82 (m, 3H), 2.22-2.06 (m, 4H), 1.80-1.59 (m, 6H), 0.93-0.82 (m, 2H), 0.41-0.20 (m, 4H) Compound 283 578.0 (DMSO-d.sup.6) δ 9.69-9.51 (m, 1H), 8.56 (br s, 1H, ), 8.18-8.01 (m, (M + H).sup.+ 2H), 7.19-7.00 (m, 2H), 4.31 (t, J = 7.4 Hz, 2H, ), 4.18 (d, J = 11.0 Hz, 2H, ), 4.06 (s, 2H, s), 3.85 (d, J = 10.9 Hz, 2H, ), 2.94 (s, 3H), 2.72 (br t, J = 7.4 Hz, 2H), 1.85-1.60 (m, 6H), 0.96-0.82 (m, 2H), 0.28 (s, 4H) Compound 284 524.0 (DMSO-d.sup.6) δ 9.61-9.52 (m, 1H), 8.50-8.22 (m, 2H), 8.12-7.73 (M + H).sup.+ (m, 2H), 7.16-6.90 (m, 2H), 4.11-3.92 (m, 2H), 3.81-3.66 (m, 1H), 3.00-2.87 (m, 3H), 2.08-1.93 (m, 2H), 1.87-1.74 (m, 2H), 1.68-1.46 (m, 10H), 1.36-1.12 (m, 3H) Compound 285 572.2 (DMSO-d.sup.6) δ 9.59 (s, 1 H) 8.15-7.91 (m, 3 H) 7.90-7.79 (m, 2 (M + H).sup.+ H) 7.77-7.70 (m, 1 H) 7.14 (m, 2 H) 3.89 (s, 2 H) 3.64-3.43 (m, 1 H) 2.95 (s, 3 H) 2.05-1.91 (m, 1 H) 1.84-1.45 (m, 9 H) 1.38- 1.05 (m, 2 H) 0.99-0.79 (m, 6 H) 0.27 (br d, J = 9.13 Hz, 4 H) Compound 287 542.1 (DMSO-d.sup.6) δ 9.60-9.54 (m, 1 H) 8.11-8.01 (m, 3 H) 7.93-7.84 (M + H).sup.+ (m, 1 H) 7.78-7.71 (m, 1 H) 7.15-7.11 (m, 2 H) 4.30-4.26 (s, 1 H) 3.96-3.83 (s, 2 H) 3.73-3.62 (m, 1 H) 2.99-2.90 (s, 3 H) 1.95-1.83 (m, 2 H) 1.74-1.63 (m, 6 H) 1.62-1.46 (m, 6 H) 0.96- 0.80 (m, 2 H) 0.34-0.20 (m, 4 H) Compound 289 556.0 (DMSO-d.sup.6) δ 9.59 (s, 1H), 8.36 (br s, 1H), 8.12-7.94 (m, 1H), (M + H).sup.+ 7.94-7.77 (m, 2H), 7.12 (d, J = 1.8 Hz, 1H), 7.10-6.96 (m, 1H), 5.28-4.60 (m, 1H), 4.01 (s, 2H), 3.73 (t, J = 6.7 Hz, 2H), 3.18 (t, J = 6.7 Hz, 2H), 1.65 (br d, J = 11.7 Hz, 5H), 1.58-1.44 (m, 2H), 1.33-1.23 (m, 3H), 1.19 (s, 9H) Compound 291 550.0 (DMSO-d.sup.6) δ 9.71-9.45 (m, 1 H), 8.44-8.28 (m, 2 H), 7.85 (br s, (M + H).sup.+ 2 H), 7.17-7.02 (m, 2 H), 4.06 (s, 2 H), 3.76 (br s, 1 H), 2.94 (s, 3 H), 2.08-1.96 (m, 2 H), 1.91-1.48 (m, 11 H), 0.88 (br d, J = 8.38 Hz, 2 H), 0.29 (br s, 4 H) Compound 292 631.2 (DMSO-d.sup.6) δ 8.20-7.97 (m, 3 H), 7.89-7.76 (m, 1 H), 7.75- (M + H).sup.+ 7.62 (m, 1 H), 7.25-7.02 (m, 2 H), 4.06-3.84 (m, 2 H), 3.27- 3.17 (m, 2 H), 3.15-2.96 (m, 2 H), 2.05-1.80 (m, 7 H), 1.78- 1.50 (m, 4 H), 1.33-1.11 (m, 9 H), 1.06-0.82 (m, 2 H), 0.47- 0.09 (m, 4 H) Compound 293 594.1 (DMSO-d.sup.6) δ 9.86-9.44 (m, 1 H), 8.55-8.22 (m, 1 H), 8.11- (M + H).sup.+ 7.86 (m, 4 H), 7.80-7.69 (m, 1 H), 7.20-7.01 (m, 2 H), 3.97- 3.78 (m, 2 H), 3.70-3.55 (m, 1 H), 3.10-2.97 (m, 2 H), 2.80- 2.67 (m, 2 H), 2.43-2.35 (m, 2 H), 1.76-1.49 (m, 6 H), 1.27- 1.10 (m, 3 H), 0.97-0.76 (m, 2 H), 0.37-0.14 (m, 4 H) Compound 295 532.1 (DMSO-d.sup.6) δ 9.62 (br s, 1 H), 8.08-7.92 (m, 3 H), 7.80 (br d, (M + H).sup.+ J = 6.63 Hz, 1 H), 7.74-7.63 (m, 2 H), 7.10 (d, J = 1.75 Hz, 2 H), 5.34 (br s, 1 H), 3.86-3.75 (m, 1 H), 3.74-3.61 (m, 1 H), 2.94 (s, 3 H), 2.22-2.04 (m, 2 H), 2.02-1.89 (m, 2 H), 1.87-1.75 (m, 1 H), 1.72-1.52 (m, 4 H), 1.09 (s, 9 H) Compound 297 576.1 (DMSO-d.sup.6) δ 9.65-9.46 (m, 1 H) 8.03-7.93 (m, 1 H) 7.87 (br d, (M + H).sup.+ J = 7.50 Hz, 1 H) 7.37-7.28 (m, 1 H) 7.25-7.18 (m, 1 H) 7.15- 7.10 (m, 1 H) 7.04 (br d, J = 8.88 Hz, 1 H) 4.00 (s, 3 H) 3.93 (s, 2 H) 2.98-2.89 (m, 3 H) 1.74-1.56 (m, 6 H) 1.10 (s, 9 H) 0.93- 0.82 (m, 2 H) 0.36-0.20 (m, 4 H) Compound 298 562.1 (DMSO-d.sup.6) δ 11.64-10.86 (m, 1 H) 9.64-9.45 (m, 1 H) 7.99- (M + H).sup.+ 7.82 (m, 1 H) 7.74-7.54 (m, 1 H) 7.23-6.81 (m, 4 H) 4.03- 3.85 (s, 2 H) 3.03-2.86 (s, 3 H) 1.75-1.56 (m, 6 H) 1.13 (s, 9 H) 0.97-0.81 (m, 2 H) 0.37-0.16 (m, 4 H) Compound 299 536.1 (DMSO-d.sup.6) δ 9.71-9.10 (m, 1 H) 8.43-8.31 (m, 1 H) 8.13-7.95 (M + H).sup.+ (m, 1 H) 7.47-7.28 (m, 1 H) 7.23-6.99 (m, 3 H) 4.40-4.17 (s, 2 H) 3.03-2.86 (s, 3 H) 1.99-1.78 (m, 2 H) 1.75-1.56 (m, 4 H) 1.26-1.13 (s, 9 H) 0.99-0.82 (m, 2 H) 0.42-0.17 (s, 4 H) Compound 301 515.1 (DMSO-d.sup.6) δ 9.08-8.37 (m, 1 H) 8.02-7.90 (m, 1 H) 7.29- (M + H).sup.+ 7.20 (m, 1 H) 7.14-6.99 (m, 2 H) 5.73-5.64 (m, 1 H) 4.65-4.53 (m, 1 H) 4.13-3.97 (m, 2 H) 2.96-2.90 (m, 3 H) 2.19-2.09 (m, 1 H) 1.86-1.37 (m, 14 H) 0.95-0.84 (m, 2 H) 0.34-0.23 (m, 4 H) Compound 302 596.0 (DMSO-d.sup.6) δ 9.66-9.49 (m, 1 H, m) 8.14-7.92(m, 2 H) 7.42 (d, (M + H).sup.+ J = 8.55 Hz, 1 H) 7.17-6.93 (m, 2 H) 4.57-4.33 (m, 4 H) 4.09- 4.00 (m, 5 H) 2.93 (s, 3 H) 1.76-1.53 (m, 6 H) 0.95-0.78 (m, 2 H) 0.36-0.17 (m, 4 H) Compound 303 582.0 (DMSO-d.sup.6) δ 11.64-11.90 (m, 1 H) 9.43-9.61 (m, 1 H) 7.69- (M + H).sup.+ 7.95 (m, 2 H) 6.93-7.18 (m, 3 H) 4.43 (t, J = 12.88 Hz, 4 H) 3.95 (s, 2 H) 2.93 (s, 3 H) 1.55-1.76 (m, 6 H) 0.76-1.01 (m, 2 H) 0.28 (s, 4H) Compound 305 509.3 (DMSO-d.sup.6) δ 9.62 (s, 1H), 8.19-7.87 (m, 1H), 7.55-7.39 (m, (M + H).sup.+ 4H), 7.16-6.94 (m, 2H), 5.18 (d, J = 4.3 Hz, 1H), 4.56-4.45 (m, 1H), 3.96-3.84 (m, 2H), 2.94 (s, 3H), 2.35-2.20 (m, 1H), 1.97- 1.47 (m, 14H), 0.89 (br d, J = 11.3 Hz, 2H), 0.27 (br d, J = 5.5 Hz, 4H) Compound 306 529.1 (DMSO-d.sup.6) δ 9.56 (br s, 1H), 8.22-7.92 (m, 1H), 7.83-7.57 (m, (M + H).sup.+ 4H), 7.19-6.95 (m, 2H), 3.89 (br s, 2H), 2.94 (s, 3H), 2.86-2.71 (m, 1H), 1.79-1.45 (m, 14H), 0.89 (br d, J = 12.0 Hz, 2H), 0.28 (br s, 4H) Compound 309 564.1 (DMSO-d.sup.6) δ 9.70-9.33 (m, 1H), 8.08-8.03 (m, 1H), 7.99 (br d, (M + H).sup.+ J = 7.8 Hz, 1H), 7.91-7.78 (m, 1H), 7.76-7.67 (m, 2H), 7.32- 7.17 (m, 1H), 3.92 (br s, 2H), 3.07-2.91 (m, 3H), 1.82-1.47 (m, 6H), 1.19-1.03 (m, 9H), 0.93-0.75 (m, 2H), 0.37-0.15 (m, 4H) Compound 310 564.1 (DMSO-d.sup.6) δ 9.81-9.25 (m, 1 H), 8.09-8.02 (m, 1 H), 8.02- (M + H).sup.+ 7.95 (m, 1 H), 7.90-7.80 (m, 1 H), 7.76-7.62 (m, 2 H), 7.32- 7.11 (m, 1 H), 4.03-3.86 (s, 2 H), 3.02-2.89 (s, 3 H), 2.05- 1.95 (m, 2 H), 1.82-1.49 (m, 4 H), 1.11 (s, 9 H), 0.89-0.70 (m, 2 H), 0.33-0.14 (m, 4 H) Compound 311 586.1 (CDCl.sub.3) δ 8.16 (br s, 1 H) 7.89 (br d, J = 7.88 Hz, 1 H) 7.21 (s, 1 H) (M + H).sup.+ 7.17 (d, J = 8.63 Hz, 1H) 7.10-6.86 (m, 1 H) 6.53-6.42 (m, 1 H) 5.62 (br d, J = 3.25 Hz, 1 H) 4.09 (s, 3 H) 3.99 (br s, 2 H) 2.99 (s, 3 H) 2.33 (s, 1 H) 1.91-1.64 (m, 12 H) 0.92 (br d, J = 11.51 Hz, 2 H) 0.31 (s, 4H) Compound 312 495.1 (DMSO-d.sup.6) δ 9.54 (br s, 1 H, ) 8.24-7.41 (m, 5 H) 7.11-6.80 (M + H).sup.+ (m, 2 H) 5.26 (d, J = 4.50 Hz, 1 H) 4.49 (dd, J = 6.88, 4.75 Hz, 1 H) 3.89 (br s, 2 H) 2.93 (s, 3 H) 2.61-2.78 (m, 1 H) 2.32-1.74 (m, 4 H, m) 1.71-1.65 (m, 8 H) 0.91-0.88 (m, 2 H) 0.28 (br s, 4 H) Compound 313 495.1 (DMSO-d.sup.6) δ 9.54 (br s, 1 H, ) 8.24-7.41 (m, 5 H) 7.11-6.80 (M + H).sup.+ (m, 2 H) 5.26 (d, J = 4.50 Hz, 1 H) 4.49 (dd, J = 6.88, 4.75 Hz, 1 H) 3.89 (br s, 2 H) 2.93 (s, 3 H) 2.61-2.78 (m, 1 H) 2.32-1.74 (m, 4 H, m) 1.71-1.65 (m, 8 H) 0.91-0.88 (m, 2 H) 0.28 (br s, 4 H) Compound 314 546.1 (DMSO-d.sup.6) δ 9.55 (br s, 1 H), 7.59-7.41 (m, 4 H), 7.13 (d, (M + H).sup.+ J = 1.88 Hz, 2 H), 5.40 (d, J = 4.50 Hz, 1 H), 4.69-4.60 (m, 1 H), 3.89 (br s, 2 H), 3.66-3.49 (m, 4 H), 2.94 (s, 3 H), 2.75 (m, 2 H), 1.73-1.54 (m, 6 H), 0.95-0.84 (m, 2 H), 0.28 (br s, 4 H) Compound 315 574.1 (DMSO-d.sup.6) δ 8.46 (br d, J = 1.59 Hz, 1 H) 7.38-7.62 (m, 5 H) 7.17 (M + H).sup.+ (d, J = 2.20 Hz, 1 H) 7.03 (m, 1 H) 4.98 (br s, 1 H) 4.79 (m, 1 H) 3.90 (s, 2 H) 2.90-2.96 (m, 3 H) 2.65-2.56 (m, 6 H)1.83-1.99 (m, 4 H) 1.56-1.80 (m, 6 H) 0.92-1.04 (m, 2 H) 0.24-0.38 (m, 4H) Compound 316 510.6 (DMSO-d.sup.6) δ 9.64 (br d, J = 5.26 Hz, 1H), 8.69-8.57 (d, 1H), 8.11- (M + H).sup.+ 7.98 (d, 1H), 7.66-7.54 (s, 1H), 7.45 (m, 1H), 7.16 (m, 2H), 5.46 (d, 1H), 4.57-4.46 (t, 1H), 3.75 (m, 2H), 2.95 (s, 3H), 1.70- 1.36 (m, 15H), 0.91-0.80 (m, 2H), 0.32-0.21 (m, 4H) Compound 317 510.3 (DMSO-d.sup.6) δ 9.56 (s, 1 H), 8.14 (d, J = 8.38 Hz, 1 H), 8.01-7.93 (M + H).sup.+ (m, 1 H), 7.74-7.66 (m, 1 H), 7.62 (d, J = 7.63 Hz, 1 H), 7.18- 7.04 (m, 2 H), 5.45 (d, J = 5.00 Hz, 1 H), 4.53-4.44 (m, 1 H), 4.35 (d, J = 11.2 Hz, 1 H), 4.12 (d, J = 11.6 Hz, 1 H), 2.95 (s, 3 H), 2.43- 2.35 (m, 1 H), 1.74-1.39 (m, 14 H), 0.95-0.79 (m, 2 H), 0.36- 0.21 (m, 4 H) Compound 318 521.2 (DMSO-d.sup.6) δ 9.66-9.46 (m, 1 H), 8.15-7.90 (m, 1 H), 7.78- (M + H).sup.+ 7.62 (m, 3 H), 7.54-7.38 (m, 2 H), 6.38-7.97 (m, 2 H), 4.01- 3.83 (s, 2 H), 3.20-3.07 (s, 4 H), 3.00-2.87 (m, 3 H), 1.83-1.43 (m, 12 H), 0.98-0.80 (m, 2 H), 0.38-0.14 (m, 4 H) Compound 319 510.1 (DMSO-d.sup.6) δ 9.60 (s, 1H), 8.58 (s, 1H), 8.05 (s, 2H), 7.37 (s, 1H), (M + H).sup.+ 7.12 (d, J = 2.1 Hz, 1H), 7.06 (brd, J = 8.5 Hz, 1H), 4.09 (s, 2H), 2.95 (s, 3H), 1.65 (br d, J = 10.5 Hz, 5H), 1.54 (br t, J = 11.4 Hz, 2H), 1.45-1.23 (m, 3H), 1.18 (s, 9H). Compound 320 586.1 (DMSO-d.sup.6) δ 9.78-9.56 (m, 1H), 8.15-7.91 (m, 4H), 7.87-7.77 (M + H).sup.+ (m, 1H), 7.21-6.97 (m, 2H), 4.26 (br t, J = 7.4 Hz, 2H), 4.09 (br d, J = 10.5 Hz, 2H), 3.89 (br s, 2H), 3.79-3.68 (m, 2H), 3.12- 3.00 (m, 2H), 2.71-2.60 (m, 2H), 1.78-1.51 (m, 6H), 1.27-1.14 (m, 3H), 0.86 (br d, J = 4.5 Hz, 2H), 0.39-0.14 (m, 4H) Compound 321 560.1 (DMSO-d.sup.6) δ 9.69-9.57 (m, 1 H) 8.14-8.00 (m, 1 H) 7.58-7.51 (M + H).sup.+ (m, 1 H) 7.50-7.43 (m, 1 H) 7.21-7.02 (m, 2 H) 4.51-4.24 (m, 2 H) 3.98-3.79 (m, 4 H) 3.00-2.92 (m, 3 H) 2.01-1.91 (m, 4 H) 1.90-1.78 (m, 2 H) 1.75 (br d, J = 2.88 Hz, 6 H) 0.97-0.88 (m, 2 H) 0.43-0.21 (m, 4H) Compound 322 565.0 (DMSO-d.sup.6) δ 9.68-9.41 (m, 1 H) 8.23-7.94 (m, 4 H) 7.88-7.76 (M + H).sup.+ (m, 1 H) 7.21-7.03 (m, 2 H) 4.35-4.17 (m, 1 H) 4.01-3.78 (m, 2 H) 3.12-2.86 (m, 7 H) 1.85-1.44 (m, 6 H) 1.04-0.75 (m, 2 H) 0.42-0.11 (m, 4H) Compound 323 (DMSO-d.sup.6) δ 8.08-7.94 (m, 2 H) 7.89-7.78 (m, 1 H) 7.76-7.69 (m, 1 H) 7.69-7.62 (m, 1 H) 7.54-7.45 (m, 1 H) 7.45-7.30 (m, 1 H) 4.69 (s, 1H) 4.01-3.87 (m, 2 H) 3.30 (s, 1H) 2.29-2.15 (m, 2 H) 2.05-1.88 (m, 6 H) 1.13-1.06 (m, 9 H) Compound 324 532.1 (DMSO-d.sup.6) δ 9.61 (br s, 1 H) 8.12-7.92 (m, 2 H) 7.90-7.76 (m, (M + H).sup.+ 1 H) 7.75-7.64 (m, 2 H) 7.18-7.03 (m, 1 H) 5.35 (br d, J = 10.08 Hz, 1 H) 4.77-4.64 (m, 1 H) 4.03-3.65 (m, 2 H) 2.95 (s, 3 H) 2.31-1.75 (m, 6H) 1.67-1.53 (m, 2 H) 1.13-1.07 (m, 9 H) Compound 325 (DMSO-d.sup.6) δ 8.45-7.95 (m, 4H), 7.90-7.74 (m, 1H), 7.57-7.26 (m, 2H), 3.91 (br s, 2H), 3.60-3.45 (m, 1H), 1.84-1.53 (m, 6H), 1.25-1.13 (m, 6H), 0.94-0.73 (m, 2H), 0.26 (br s, 4H) Compound 326 517.1 (DMSO-d.sup.6) δ 9.74-9.46 (m, 1H), 8.19-7.93 (m, 4H), 7.82 (t, J = (M + H).sup.+ 7.8 Hz, 1H), 7.26-6.96 (m, 2H), 4.10-3.81 (m, 2H), 3.61-3.43 (m, 1H), 2.94 (s, 3H), 1.82-1.47 (m, 6H), 1.29-1.04 (m, 6H), 0.97-0.78 (m, 2H), 0.27 (br s, 4H) Compound 327 570.0 (DMSO-d.sup.6) δ 9.69 (br s, 1H), 8.23-7.93 (m, 3H), 7.91-7.79 (m, (M + H).sup.+ 1H), 7.76-7.59 (m, 2H), 7.24-7.01 (m, 2H), 4.12-3.89 (m, 2H), 3.07 (q, J = 7.0 Hz, 2H), 2.04 (br s, 2H), 1.82 (br d, J = 11.9 Hz, 6H), 1.27-1.16 (m, 3H), 1.13 (s, 9H) Compound 329 552.2 (CD.sub.3OD) δ 8.41-7.98 (m, 3 H) 7.66-7.88 (m, 2 H) 7.03-7.34 (M + H).sup.+ (m, 2 H) 3.83-4.09 (m, 2 H) 2.95 (s, 3 H) 1.99-2.15 (m, 2 H) 1.73-1.96 (m, 3 H) 1.44-1.70 (m, 4 H) 1.30-1.39 (m, 2 H) 1.17- 1.25 (m, 9H) Compound 330 549.3 (DMSO-d.sup.6) δ 9.53-9.62 (m, 1 H) 8.55-8.67 (m, 1 H) 7.94-8.16 (M + H).sup.+ (m, 2 H) 7.00-7.18 (m, 2 H) 4.05-4.11 (m, 2 H) 3.87-3.98 (m, 1 H) 2.90-2.98 (m, 3 H) 1.90-1.99 (m, 4 H) 1.51-1.82 (m, 12 H) 0.25-0.34 (m, 4 H) Compound 331 523.2 (CDCl.sub.3) δ 9.73-9.43 (m, 1H), 8.30-7.83 (m, 1H), 7.75-7.53 (M + H).sup.+ (m, 2H), 7.51-7.31 (m, 2H), 7.23-6.88 (m, 2H), 4.87 (s, 1H), 4.07-3.77 (m, 2H), 2.93 (s, 3H), 2.29-2.15 (m, 1H), 1.78-1.33 (m, 15H), 1.31-1.01 (m, 2H), 0.98-0.80 (m, 2H), 0.42-0.13 (m, 4H) Compound 332 497.3 (DMSO-d.sup.6) δ 8.11-7.90 (m, 3 H) 7.87-7.79 (m, 1 H) 7.75-7.67 (M + H).sup.+ (m, 2 H) 7.29 (s, 2 H) 5.14 (br d, J = 2.25 Hz, 1 H) 4.71 (br d, J = 3.13 Hz, 1 H) 3.88 (br d, J = 8.76 Hz, 2 H) 1.83-1.54 (m, 6 H) 1.35-1.25 (m, 3H) 1.11 (s, 9 H) 0.92-0.77 (m, 2 H) 0.33-0.19 (m, 4H) Compound 333a 584.1 (DMSO-d.sup.6) δ 9.77-9.61 (m, 1 H) 8.10-7.92 (m, 3 H) 7.82 (br s, (M + H).sup.+ 3 H) 7.19-7.03 (m, 2 H) 6.05-5.04 (m, 1 H) 3.92-3.75 (m, 2 H) 3.11-2.97 (m, 2 H) 2.01-1.55 (m, 7 H) 1.25 (br s, 14 H) Compound 333b 584.1 (DMSO-d.sup.6) δ 9.71-9.59 (m, 1 H) 8.08-7.91 (m, 3 H) 7.87-7.63 (M + H).sup.+ (m, 3 H) 7.42-7.35 (m, 1 H) 7.20-7.01 (m, 1 H) 6.28-5.96 (m, 1 H) 3.82-3.74 (m, 1 H) 3.08-3.00 (m, 2 H) 1.96-1.77 (m, 2 H) 1.97-1.49 (m, 9 H) 1.25-1.06 (m, 12 H) Compound 335 543.1 (DMSO-d.sup.6) δ 9.65-9.52 (m, 1 H), 8.17-7.92 (m, 4 H), 7.84- (M + H).sup.+ 7.75 (m, 1 H), 7.20-7.04 (m, 2 H), 4.00-3.79 (m, 2 H), 3.60- 3.49 (m, 2 H), 3.01-2.88 (m, 3 H), 1.94-1.46 (m, 13 H), 0.95- 0.79 (m, 2 H), 0.26 (br d, J = 8.76 Hz, 4 H) Compound 336a 580.1 (DMSO-d.sup.6) δ 9.71-9.53 (m, 1 H) 8.81-8.69 (m, 1 H) 8.10- (M + H).sup.+ 7.67(m, 5 H) 7.17-6.99 (m, 2 H) 6.03-5.65 (m, 1 H) 3.92-3.73 (m, 2 H) 2.97-2.93 (m, 3 H) 2.26 (s, 1 H) 1.79-1.60 (m, 13 H) 1.12-0.91 (m, 2H) Compound 336b 580.1 (DMSO-d.sup.6) δ 9.67-9.42 (m, 1 H) 8.83-8.64 (m, 1 H) 8.15-7.65 (M + H).sup.+ (m, 5 H) 7.40-7.34 (m, 1 H) 7.18-7.00 (m, 1 H) 6.33-5.97 (m, 1 H) 3.88-3.72 (m, 2 H) 2.97-2.93 (m, 3 H) 2.30-2.29 (m, 1 H) 1.85-1.53 (m, 15 H) Compound 337 574.1 (DMSO-d.sup.6) δ 9.65-9.50 (m, 1 H) 9.15-9.00 (m, 1 H) 8.05-7.95 (M + H).sup.+ (m, 2 H) 7.60 (dd, J = 9.88, 8.63 Hz, 1 H) 7.19-7.00 (m, 2 H) 3.91 (br s, 2 H) 2.94 (s, 3 H) 2.29 (s, 1 H) 1.75 (s, 6 H) 1.71-1.54 (m, 6 H) 0.92-0.80 (m, 2 H) 0.26 (br d, J = 6.75 Hz, 4 H) Compound 338 551.1 (DMSO-d.sup.6) δ 8.13-7.95 (m, 2 H), 7.90-7.79 (m, 1 H), 7.76- (M + H).sup.+ 7.64 (m, 2 H), 7.45-7.26 (m, 2 H), 6.87-6.74 (m, 1 H), 5.22- 5.08 (s, 1 H), 4.01-3.82 (s, 2 H), 1.84-1.49 (m, 6 H), 1.19-1.03 (m, 9 H), 0.93-0.79 (m, 2 H), 0.38-0.16 (m, 4 H) Compound 339 518.1 (DMSO-d.sup.6) δ 9.62-9.52 (m, 1H), 8.16-7.93 (m, 1H), 7.71-7.50 (M + H).sup.+ (m, 4H), 7.18-7.03 (m, 2H), 4.31-4.22 (m, 1H), 3.96-3.84 (m, 2H), 3.35 (s, 1H), 2.99-2.91 (m, 3H), 2.46-2.31 (m, 1H), 1.81- 1.74 (m, 1H), 1.65 (br s, 6H), 1.60-1.39 (m, 5H), 1.32-1.20 (m, 1H), 0.94-0.82 (m, 2H), 0.37-0.19 (m, 4H) Compound 340 578.1 (DMSO-d.sup.6) δ 9.72-9.60 (m, 1 H), 8.11-7.88 (m, 3 H), 7.62- (M + H).sup.+ 7.50 (m, 1 H), 7.18-6.99 (m, 2 H), 3.97-3.80 (s, 2 H), 3.11- 2.97 (s, 2 H), 1.75-1.50 (m, 6 H), 1.25-1.08 (m, 12 H), 0.93- 0.79 (m, 2 H), 0.37-0.18 (m, 4 H) Compound 341 558.1 (DMSO-d.sup.6) δ 9.86-9.10 (m, 1 H) 8.54-7.75 (m, 1 H) 7.56-7.42 (M + H).sup.+ (m, 4 H) 7.21-6.80 (m, 2 H) 3.99-3.85 (m, 2 H) 3.83-3.54 (m, 1 H) 3.50-3.38 (m, 2 H) 2.95-2.92 (m, 3 H) 1.95-1.86 (m, 4 H) 1.77-1.49 (m, 8 H) 1.39-1.33 (m, 3 H) 0.92-0.82 (m, 2 H) 0.32- 0.23 (m, 4 H) Compound 342 545.1 (DMSO-d.sup.6) δ 9.66-9.54 (m, 1H), 8.20-8.09 (m, 1H), 8.04-7.93 (M + H).sup.+ (m, 1H), 7.73 (br d, J = 7.6 Hz, 1H), 7.65-7.53 (m, 1H), 7.20- 7.03 (m, 2H), 4.27-4.16 (m, 2H), 3.79-3.72 (m, 2H), 3.02-2.86 (s, 3H), 2.69-2.55 (m, 4H), 2.05-1.91 (m, 4H), 1.75-1.57 (m, 6H), 0.95-0.85 (m, 2H), 0.39-0.19 (m, 4H) Compound 343 560.1 (CD.sub.3OD) δ 8.18 (d, J = 8.63 Hz, 1 H) 7.68 (s, 1 H) 7.26-7.12 (m, 2 (M + H).sup.+ H) 4.28-4.05 (m, 4 H) 3.12-2.91 (m, 7 H) 2.67 (s, 3 H) 2.25- 2.06 (m, 4 H) 1.92-1.64 (m, 6 H) 0.95 (br d, J = 12.76 Hz, 2 H) 0.42-0.27 (m, 4 H) Compound 345 516.2 (CD.sub.3OD) δ δ 8.07 (m, 1H), 7.56-7.53 (m, 4H), 7.20-7.10 (m, 2H), (M + H).sup.+ 4.03-3.90(m, 4H), 3.82-3.72 (m, 4H), 2.92 (s, 3H), 1.85-1.61 (m, 6 H), 0.97-0.94 (m, 2H), 0.26 (brs, 4H) Compound 346 496.1 (DMSO-d.sup.6) δ 9.83 (s, 1H), 8.03-8.00 (br s, 1H), 7.50-7.43 (m, (M + H).sup.+ 4H), 7.12-6.97 (m, 2H), 4.01 (s, 2H), 3.71-3.90(m, 2H), 3.02-2.97 (m, 1H), 2.93 (s, 3), 2.81 (m, 1 H), 2.22-2.19 (m, 2H), 1.65 (m, 6H), 0.94-0.88 (m, 2H), 0.27 (br s, 4H) Compound 347 494.1 (DMSO-d.sup.6) δ 9.54-9.48 (m, 1 H) 7.20-7.10 (m, 2 H) 7.07-6.94 (M + H).sup.+ (m, 1 H) 6.72-6.62 (m, 3 H) 5.88-5.81 (m, 1 H) 3.93-3.86 (m, 2 H) 3.76-3.66 (m, 1 H) 2.94-2.91 (m, 3 H) 1.96-1.86 (m, 2 H) 1.73-1.59 (m, 8 H) 1.58-1.51 (m, 2 H) 1.48-1.39 (m, 2 H) 0.99- 0.84 (m, 2 H) 0.32-0.24 (m, 4 H) Compound 348 508.1 (DMSO-d.sup.6) δ 9.29-8.82 (s, 1 H), 7.65-7.44 (s, 1 H), 7.31-7.24 (M + H).sup.+ (m, 1 H), 7.18-7.13 (m, 1 H), 7.02-6.99 (m, 1 H), 6.97-6.90 (m, 2 H), 6.80-6.74 (m, 1 H), 4.26-4.16 (m, 1 H), 3.94-3.87 (s, 2 H), 2.94-2.91 (s, 3 H), 2.80-2.76 (s, 3 H), 1.89-1.79 (m, 2 H), 1.75-1.55 (m, 12 H), 1.02-0.94 (m, 2 H), 0.35-0.25 (m, 4 H) Compound 349 530.1 (DMSO-d.sup.6) δ 9.26 (s, 1 H), 7.56-7.45 (m, 5 H), 7.17 (d, J = 2.20 (M + H).sup.+ Hz, 1 H), 7.03 (dd, J = 8.50, 1.77 Hz, 1 H), 3.90 (s, 2 H), 3.74 (s, 2 H), 2.94 (s, 3 H), 2.93-2.89 (m, 2 H), 2.81-2.75 (m, 2 H), 2.31- 2.21 (m, 2 H), 1.75-1.61 (m, 6 H), 0.97 (br d, J = 13.33 Hz, 2 H), 0.32-0.26 (m, 4 H) Compound 351 531.1 (DMSO-d.sup.6) δ 9.35-9.17 (m, 1H), 7.61-7.39 (m, 5H), 7.17 (d, J = (M + H).sup.+ 2.1 Hz, 1H), 7.06-6.96 (m, 1H), 5.48-5.35 (m, 1H), 4.70-4.57 (m, 1H), 3.97-3.82 (m, 2H), 2.93 (s, 3H), 2.45-2.33 (m, 3H), 1.80-1.55 (m, 6H), 0.97 (br d, J = 13.3 Hz, 2H), 0.43-0.23 (m, 4H) Compound 352 499.1 (DMSO-d.sup.6) δ 9.63-9.48 (m, 1 H) 8.02 (br d, J = 7.13 Hz, 1 H) 7.23 (M + H).sup.+ (d, J = 3.38 Hz, 1 H) 7.14-7.10 (m, 1 H) 7.06 (dd, J = 8.76, 2.00 Hz, 1 H) 6.48 (d, J = 3.38 Hz, 1 H) 5.51 (d, J = 5.25 Hz, 1 H) 4.48-4.35 (m, 1 H) 4.35-4.23 (m, 2 H) 2.94 (s, 3 H) 2.35-2.25 (m, 1 H) 1.88-1.68 (m, 7H) 1.61-1.19 (m, 7 H) 0.92 (br d, J = 13.26 Hz, 2 H) 0.32 (s, 4 H) Compound 353 (DMSO-d.sup.6) δ 11.68 (s, 1 H) 9.55 (br s, 1 H) 8.11-7.76 (m, 3 H) 7.70-7.55 (m, 1 H) 7.20-6.97 (m, 2 H) 3.91 (br s, 2 H) 3.84-3.72 (m, 1 H) 3.32 (s, 2 H) 2.93 (s, 3 H) 2.58-2.55 (m, 1 H) 2.14-1.90 (m, 4 H) 1.71-1.60 (br s, 6 H), 1.55 (br s, 3 H) 0.95-0.80 (m, 2 H) 0.27 (br s, 4 H) Compound 354 509.2 (DMSO-d.sup.6) δ 9.53 (s, 1 H) 8.0 (br m, 1 H) 7.58-7.30 (m, 4 H) (M + H).sup.+ 7.20-6.87 (m, 2 H) 5.32 (d, J = 4.0 Hz, 1H) 4.47 (d, J = 3.6 Hz, 1 H) 3.89 (br s, 2 H) 2.93 (s, 3 H) 2.30-2.18 (m, 2 H) 1.93-1.78 (m, 1 H) 1.75-1.25 (m, 9 H) 0.95 (s, 3H) 0.85-0.75 (m, 2 H) 0.28 (br s, 4H) Compound 355 546.1 (DMSO-d.sup.6) δ 9.50-9.11 (m, 1 H) 7.70-7.39 (m, 4 H) 7.27-7.22 (M + H).sup.+ (m, 1 H) 7.18-7.15 (m, 1 H) 7.07-7.01 (m, 1 H) 3.95-3.84 (m, 2 H) 2.97-2.91 (m, 3 H) 1.79-1.61 (m, 6 H) 1.34-1.30 (m, 9 H) 1.02-0.91 (m, 2 H) 0.37-0.21 (m, 4 H) Compound 356 594.0 (DMSO-d.sup.6) δ 9.69-9.35 (m, 1 H) 8.13-7.90 (m, 3 H) 7.83-7.73 (M + H).sup.+ (m, 1 H) 7.20-7.05 (m, 2 H) 4.02-3.80 (m, 3 H) 3.00-2.90 (m, 3 H) 2.83-2.63 (m, 7 H) 1.78-1.48 (m, 6 H) 0.96-0.80 (m, 2 H) 0.42-0.11 (m, 4 H) Compound 357 511.3 (DMSO-d.sup.6) δ 9.58-9.50 (m, 1 H) 8.11-7.91 (m, 1 H) 7.54-7.39 (M + H).sup.+ (m, 4 H) 7.17-6.98 (m, 2 H) 5.09 (d, J = 4.63 Hz, 1 H) 4.72 (m, 1 H) 3.89 (br s, 2 H) 2.97-2.90 (m, 3 H) 1.73-1.41 (m, 8 H) 0.94 (s, 9 H) 0.91-0.84 (m, 2 H) 0.32-0.21 (m, 4 H) Compound 358 542.1 (DMSO-d.sup.6) δ 9.53 (brs 1H), 8.06-7.99 (m, 1H), 7.53-7.44 (m, 4H), (M + H).sup.+ 7.15 (s, 1H), 7.12-7.04 (m, 1H), 3.96 (s, 2H), 3.89 (s, 2H), 3.03- 2.96 (m, 2H), 2.85-2.80 (m, 2H), 2.33-2.30 (m, 2 H), 1.78-1.54 (m, 6H), 0.96-0.88 (m, 2H), 0.38-0.28 (m, 4H) Compound 359 576.1 (DMSO-d.sup.6) δ 9.79-9.47 (m, 1 H) 8.18-7.95 (m, 2 H) 7.88-7.78 (M + H).sup.+ (m, 1 H) 7.76-7.63 (m, 1 H) 7.57-7.40 (m, 1 H) 7.22-6.99 (m, 2 H) 4.87-4.61 (m, 1 H) 4.05-3.77 (m, 2 H) 3.29-3.14 (m, 2 H) 3.11-2.94 (m, 2 H) 1.96-1.45 (m, 6 H) 1.29-1.14 (m, 3 H) 1.12- 0.96 (m, 6 H) 0.95-0.81 (m, 2 H) 0.47-0.07 (m, 4 H) Compound 361a 588.1 (DMSO-d.sup.6) δ 9.64 (s, 1 H) 8.13-8.02 (m, 1 H) 7.98 ( d, J = 8 Hz, 1 (M + H).sup.+ H) 7.82 ( d, J = 6 Hz, 1 H) 7.75-7.70 (m, 1 H) 7.67 (s, 1 H) 7.13 (d, J = 2 Hz, 2 H) 3.86 ( s, 2 H) 2.95 (s, 3 H) 2.45 (d, J = 1.2 Hz, 1 H) 1.90-1.61 (m, 6 H) 1.22-1.02 (m, 11 H) Compound 361b 588.1 (DMSO-d.sup.6) δ 9.68 (s, 1 H) 8.06-7.92 (m, 2 H) 7.83 (d, J = 6.8 Hz, (M + H).sup.+ 1 H) 7.74-7.64 (m, 2 H) 7.37 (d, J = 1.8 Hz, 1 H) 7.25-7.00 (m, 1 H) 3.78 (s, 2 H) 2.95 (s, 3 H) 2.46-2.29 (m, 1 H) 1.89-1.52 (m, 8 H) 1.11 (s, 9 H) Compound 362 541.2 (DMSO-d.sup.6) δ 9.19 (s, 1 H) 7.95-7.84 (m, 2 H) 7.80-7.50 (m, 3 (M + H).sup.+ H) 7.20-7.15 (m, 1 H) 7.10-6.98 (m, 1 H) 3.99-3.85 (m, 2 H) 3.06-3.01 (m, 1 H) 2.98-2.90 (m, 3 H) 2.23-1.99 (m, 3 H) 1.91- 1.49 (m, 14 H) 1.01-0.90 (m, 2 H) 0.36-0.23 (m, 4 H) Compound 364 515.1 (DMSO-d.sup.6) δ 9.52 (br s, 1 H) 7.94 (br d, J = 5.38 Hz, 1 H) 7.73 (s, (M + H).sup.+ 1 H) 7.59 (s, 1 H) 7.13 (d, J = 2.00 Hz, 1 H) 7.06 (dd, J = 8.63, 2.13 Hz, 1 H) 5.23 (d, J = 5.13 Hz, 1 H) 4.42 (dd, J = 7.19, 5.32 Hz, 1 H) 4.26 (s, 2 H) 2.94 (s, 3 H) 2.24-2.09 (m, 1 H) 1.88-1.63 (m, 7 H) 1.60-1.36 (m, 6 H) 1.34-1.17 (m, 1 H) 0.93 (br d, J = 12.13 Hz, 2 H) 0.32 (s, 4 H) Compound 365 568.3 (DMSO-d.sup.6) δ 9.92-9.74 (m, 1 H) 8.09-7.93 (m, 2 H) 7.83 (br d, (M + H).sup.+ J = 4.75 Hz, 1 H) 7.75-7.63 (m, 2 H) 7.16-7.05 (m, 2 H) 4.80 (t, J = 5.19 Hz, 1 H) 4.69 (t, J = 5.19 Hz, 1 H) 3.88 (br s, 2 H) 3.58- 3.43 (m, 2H) 1.72-1.49 (m, 6H) 1.11 (s, 9 H) 0.88 (br d, J = 11.26 Hz, 2 H) 0.27 (br s, 4 H) Compound 367 513.3 (DMSO-d.sup.6) δ 9.62 (s, 1 H) 8.01 (br d, J = 8.50 Hz, 1 H) 7.22 (d, (M + H).sup.+ J = 3.50 Hz, 1 H) 7.14 (d, J = 2.13 Hz, 1 H) 7.06 (m, 1 H) 6.48 (d, J = 3.38 Hz, 1 H) 5.50 (d, J = 5.50 Hz, 1 H) 4.41 (m, 1 H) 4.36-4.25 (m, 2 H) 3.04 (m, 2 H) 2.37-2.24 (m, 1 H) 1.90-1.62 (m, 7 H) 1.62-1.42 (m, 6 H) 1.38-1.26 (m, 1 H) 1.19 (t, J = 7.38 Hz, 3 H) 0.93 (br d, J = 13.26 Hz, 2 H) 0.32 (s, 4 H) Compound 368 529.2 (DMSO-d.sup.6) δ 9.63-9.47 (m, 1 H) 8.01 (br d, J = 9.38 Hz, 1 H) 7.23 (M + H).sup.+ (d, J = 3.50 Hz, 1 H) 7.14 (d, J = 2.25 Hz, 1 H) 7.06 (m, 1 H) 6.48 (d, J = 3.38 Hz, 1 H) 5.50 (d, J = 5.50 Hz, 1 H) 4.92 (br t, J = 7.13 Hz, 1 H) 4.41 (m, 1 H) 4.31 (d, J = 2.25 Hz, 2 H) 3.74 (br t, J = 6.07 Hz, 2 H) 3.19 (t, J = 6.75 Hz, 2 H) 1.92-1.45 (m, 13 H) 1.39-1.21 (m, 1 H) 1.01-0.85 (m, 2 H) 0.33 (s, 4 H) Compound 369 521.0 (DMSO-d.sup.6) δ 9.54 (br d, J = 3.25 Hz, 1 H) 8.06-7.97 (1 H, m) (M + H).sup.+ 7.25 (d, J = 3.38 Hz, 1 H) 7.13 (d, J = 2.13 Hz, 1 H) 7.06 (m, 1 H) 6.53 (d, J = 3.63 Hz, 1 H) 5.90 (d, J = 5.75 Hz, 1 H) 4.70-4.61 (m, 1 H) 4.29 (s, 2 H, ) 2.94 (s, 3 H) 2.54-2.64 (m, 5 H) 1.81-1.96 (m, 2 H) 1.76-1.62 (m, 4 H) 0.93 (br d, J = 13.76 Hz, 2 H) 0.32 (s, 4 H) Compound 370 (DMSO-d.sup.6) δ 8.15-7.92 (m, 1 H) 7.51-7.46 (m, 1 H) 7.43-7.35 (m, 1 H) 7.31-7.25 (m, 1 H) 6.58-6.33 (m, 1 H) 5.65-5.40 (m, 1 H) 4.35-4.32 (m, 2 H) 2.04-1.73 (m, 5 H) 1.70-1.33 (m, 3 H) 0.94 (s, 9 H) 0.38-0.24 (m, 4 H) Compound 371 517.3 (DMSO-d.sup.6) δ 9.70-9.42 (m, 1 H) 8.15-7.94 (m, 1 H) 7.31-7.18 (M + H).sup.+ (m, 1 H) 7.16-7.10 (m, 1 H) 7.08-6.97 (m, 1 H) 6.52-6.39 (m, 1 H) 5.58-5.45 (m, 1 H) 5.03-4.81 (m, 1 H) 4.38-4.24 (m, 3 H) 3.83-3.63 (m, 2 H) 3.24-3.11 (m, 2 H) 1.93-1.77 (m, 2 H) 1.76- 1.58 (m, 4 H) 0.98-0.91 (m, 11 H) 0.39-0.25 (m, 4 H) Compound 372 501.1 (DMSO-d.sup.6) δ 9.62 (s, 1H), 8.03 (br d, J = 8.6 Hz, 1H), 7.31-6.91 (M + H).sup.+ (m, 3H), 6.47 (d, J = 3.4 Hz, 1H), 5.51 (d, J = 4.9 Hz, 1H), 4.38- 4.22 (m, 3H), 3.13-2.98 (m, 2H), 1.93-1.57 (m, 6H), 1.19 (t, J = 7.3 Hz, 3H), 1.06-0.86 (m, 11H), 0.32 (s, 4H) Compound 373 487.3 9.55 (s, 1 H) 8.05 (br d, J = 8.58 Hz, 1H) 7.31-7.20 (m, 1H) 7.15- (M + H).sup.+ 7.00 (m, 2 H) 6.47 (d, J = 3.46 Hz, 1 H) 5.52 (d, J = 4.89 Hz, 1 H) 4.39-4.24 (m, 3 H) 2.94 (s, 3 H) 1.93-1.58 (m, 6 H) 1.00-0.83 (m, 11 H) 0.38-0.26 (m, 4 H)
Biological Assays
Inhibition of KIF18A Microtubule-Dependent ATPase Activity:
[0524] Test compounds were plated in a 3×dilution scheme in a 384-well plate. Assay buffer: 80 mM PIPES (pH 6.9), 1 mM MgCl.sub.2, 75 mM KCl, 1 mM EGTA, 1 mM DTT, 0.01% BSA, 0.005% Tween-20, 1 μM Taxol in H.sub.2O. To 50 nL of compound in DMSO was added 2.5 μL of enzyme mix [4 nM hKIF18A (1-374) in assay buffer]. After incubation at room temperature for 30 min, 2.5 μL of microtubule mix was added [0.2 mg/mL pre-formed microtubules, 2.0 mM ATP in assay buffer], the plate was centrifuged for 30 s and then incubated at 28° C. for 60 min. 5 μL of Promega® ADP-Glo Max R1 was added, the plate was centrifuged for 30 s, and the mixture incubated for 4 h at room temperature. 10 μL of Promega® ADP-Glo Max R2 was added, the plate centrifuged for 30 s, and incubated for 60 min at room temperature. Luminescence was measured with an Envision plate reader, and % Inhibition was calculated for each well as: ([max−min]−[test−min])/[max−min]. IC.sub.50 values were calculated from concentration vs. % Inhibition data via a four-parameter variable slope model.
[0525] Table 9 indicates that compounds as provided herein are potent inhibitors of KIF18a. As a comparison, the data for AMG650 (2-{6-azaspiro[2.5]octan-6-yl}-N-[2-(4,4-difluoropiperidin-1-yl)-6-methylpyrimidin-4-yl]-4-(2-hydroxyethanesulfonamido)benzamide) is 17 nM.
Binding Kinetics to KIF18a-Microtubule Complex
[0526] Compound binding kinetics parameters (k.sub.on and k.sub.off) were determined by the method of global progress curve analysis (GPCA). KIF18A (0.25 nM) was incubated for up to 24 hr with serially diluted compound in the assay buffer containing 80 mM PIPES, pH 6.9, 1 mM ATP, 0.1 mg/ml preformed microtubule from porcine brain (Cytoskeleton), 1 mM MgCl.sub.2, 1 μM Taxol, 75 mM KCl, 1 mM EGTA, 1 mM DTT, 0.01% BSA and 0.005% Tween-20. ADP product levels were determined by the Promega® ADP-Glo assay. The time/dose-dependent progress curves were then globally fit to a Michaelis-Menten kinetics model with 1-step slow binding inhibition to derive both on-rate k.sub.on and off-rate k.sub.off values (Zhang, R., Wong, K. (2017): “High performance enzyme kinetics of turnover, activation and inhibition for translational drug discovery”, Expert Opinion on Drug Discovery, 2017 January; 12(1):17-37. doi: 10.1080/17460441.2017.1245721).
[0527] Results from the binding kinetics assay are summarized in Table 10. The data in Table 10 indicate that compounds as provided herein can achieve sub-nanomolar potency with small off-rates, or very long dissociation half-life (ln(2)/k.sub.off). As a comparison, the data for AMG650 (2-{6-azaspiro[2.5]octan-6-yl}-N-[2-(4,4-difluoropiperidin-1-yl)-6-methylpyrimidin-4-yl]-4-(2-hydroxyethanesulfonamido)benzamide) are: k.sub.on=0.059 nM.sup.−1h.sup.−1; k.sub.off=0.21 h.sup.−1, dissociation t.sub.1/2=4.1 h; K.sub.1=3.4 nM.
Cell Viability of KIF18a-Sensitive Cell Lines
[0528] Cell lines were seeded as follows 24 hours before compound treatment: HCC15 (Korean Cell Line Bank) 600 cell/well, 95 μL of RPMI-1640 media supplemented with 100 units/mL penicillin, 100 units/mL streptomycin and 10% FBS; NIH:OVCAR-3 (ATCC), 1000 cell/well, 95 μL of RPMI-1640 media supplemented with 100 units/mL penicillin, 100 units/mL streptomycin, 0.01 mg/mL bovine insulin, and 20% FBS; JIMT-1 (Addexbio) 1000 cell/well, 95 μL of DMEM media supplemented with 100 units/mL penicillin, 100 units/mL streptomycin, and 10% FBS.
[0529] Test compounds were added to cells in a 20×dilution scheme by adding 5 μL of serially diluted compound to the plate, and the treated cells were incubated for an additional 7 days in a 37° C., 5% CO.sub.2 incubator. DMSO was used as the negative control (0% effect), and wells omitting cells were used as the positive control (100% effect). The cells were incubated for seven days, and cell viability determined via the Promega Cell Titre-Glo® Assay kit. Luminescence units were converted to ATP concentrations via an ATP standard curve (10 point, 2-fold dilution from 5 uM). % Inhibition was calculated for each well as: ([max−min]−[test−min])/[max−min]. IC.sub.50 values were calculated from concentration vs. % Inhibition data via a four-parameter variable slope model. Results from the biological assay are summarized in Table 10.
[0530] Table 11 indicates that compounds as provided herein potently inhibit cell growth or induce cell killing for KIF18a-sensitive cancer cell lines. As a comparison, the data for AMG650 (2-{6-azaspiro[2.5]octan-6-yl}-N-[2-(4,4-difluoropiperidin-1-yl)-6-methylpyrimidin-4-yl]-4-(2-hydroxyethanesulfonamido)benzamide) are: HCC-15, 0.066 μM; JIMT-1 0.13 μM; NIH: OVCAR3 0.10 μM.
TABLE-US-00018 TABLE 9 Summary of biochemical assay data Compound IC.sub.50 (μM) Compound 1 1.6 Compound 3 1.6 Compound 4 0.36 Compound 6 0.58 Compound 8 0.94 Compound 9 1.0 Compound 10 0.27 Compound 15 0.78 (n = 1) 0.74 (n = 2) Compound 18 0.079 Compound 19 0.032 Compound 20 0.013 Compound 21 0.019 Compound 22 0.011 (n = 3) 0.0094 (n = 10) Compound 23 0.023 Compound 24 0.010 Compound 24a 0.011 Compound 24b 0.014 Compound 25 0.12 Compound 26 0.067 Compound 27 0.083 Compound 28 0.010 Compound 29 0.022 Compound 30 0.18 Compound 31 0.039 Compound 32 0.078 Compound 42 1.3 Compound 43 0.089 Compound 45 0.27 Compound 46 0.12 Compound 48 0.10 Compound 49 0.13 Compound 50 0.072 Compound 55 0.14 Compound 57 1.1 Compound 59 1.0 Compound 60 1.2 Compound 67 0.46 Compound 70 0.030 Compound 71 0.086 Compound 83 0.13 Compound 95 0.17 Compound 96 0.10 Compound 97 0.85 Compound 107 0.47 Compound 129 0.045 Compound 134 0.016 Compound 140 0.013 Compound 141 1.1 Compound 144 0.051 Compound 145 0.29 Compound 146 0.19 Compound 147 0.043 Compound 148 0.012 Compound 149 0.078 Compound 151 0.0068 Compound 153 0.018 Compound 155 0.0074 Compound 157 0.058 Compound 159 0.019 Compound 160 0.020 Compound 162a 0.015 Compound 162b 0.037 Compound 163 0.020 Compound 164 0.12 Compound 165 0.015 Compound 165a 0.0088 Compound 165b 0.010 Compound 166 1.1 Compound 168 0.0055 Compound 170 0.015 Compound 172 0.0055 Compound 174 0.056 Compound 176 0.0056 Compound 178 0.017 Compound 180 0.011 Compound 182 0.0073 Compound 184 0.033 Compound 186 0.012 Compound 188 0.075 Compound 190 0.0048 Compound 192 0.010 Compound 194 0.050 Compound 196 0.010 Compound 198 0.026 Compound 200 0.072 Compound 202 0.053 Compound 204 0.013 Compound 206 0.027 Compound 208 0.064 Compound 210 0.016 Compound 212 0.012 Compound 214 0.08 Compound 216 0.0093 Compound 218 0.10 Compound 220 0.025 Compound 222 0.10 Compound 223 0.0067 Compound 224 0.023 Compound 225 0.0075 Compound 226 0.013 Compound 227 0.0072 Compound 228 0.0046 Compound 229 0.0062 Compound 230 0.014 Compound 231 0.0087 Compound 233 0.012 Compound 235 0.022 Compound 237 0.011 (R)-Compound 239 0.0093 (S)-Compound 239 0.015 Compound 240 0.040 Compound 241 0.18 Compound 243 0.14 Compound 245 0.034 Compound 247 0.021 Compound 249 0.0090 (R)-Compound 249 0.011 (S)-Compound 249 0.016 Compound 250 0.67 Compound 252 0.034 Compound 254 0.010 Compound 255 0.063 Compound 257 0.0083 Compound 258 0.014 Compound 260 0.012 Compound 261 0.0093 Compound 262 0.0059 Compound 264 0.035 Compound 266 0.016 Compound 268 0.077 Compound 269 0.079 Compound 270 0.110 Compound 272 0.038 Compound 274 0.0060 Compound 275 0.0080 Compound 277 0.041 Compound 279 0.0063 Compound 281 0.013 Compound 283 0.018 Compound 284 0.026 Compound 285 0.011 Compound 287 0.017 Compound 287a 0.034 Compound 287b 0.012 Compound 289 0.017 Compound 291 0.0058 Compound 292 0.022 Compound 293 0.017 Compound 295 0.038 Compound 297 0.017 Compound 298 0.0084 Compound 299 0.014 Compound 300 0.031 Compound 301 0.021 Compound 302 0.019 Compound 303 0.0082 Compound 305 0.0089 Compound 305a 0.0081 Compound 305b 0.0068 Compound 306 0.033 Compound 309 0.0065 Compound 310 0.0066 Compound 311 0.0052 Compound 313 0.020 Compound 313a 0.019 Compound 313b 0.015 Compound 314 0.028 Compound 315 0.053 Compound 316 0.018 Compound 316a 0.021 Compound 316b 0.016 Compound 317 0.011 Compound 317a 0.011 Compound 317b 0.010 Compound 318 0.93 Compound 319 1.2 Compound 320 0.018 Compound 321 0.0063 Compound 322 0.021 Compound 324 0.021 Compound 326 0.050 Compound 327 0.044 Compound 329 0.072 Compound 330 0.012 Compound 331 0.035 Compound 332 0.15 Compound 333a 0.018 Compound 333b 0.033 Compound 335 0.0093 Compound 336a 0.0085 Compound 336b 0.017 Compound 337 0.0088 Compound 338 0.049 Compound 338a 0.048 Compound 338b 0.083 Compound 339 0.024 Compound 340 0.018 Compound 341 0.025 Compound 341a 0.030 Compound 341b 0.024 Compound 342 0.020 Compound 343 0.81 Compound 345 0.058 Compound 346 0.31 Compound 347 0.28 Compound 348 0.19 Compound 349 0.045 Compound 351 0.0088 Compound 351a 0.0087 Compound 351b 0.012 Compound 352 0.0050 Compound 352a 0.0040 Compound 352b 0.0033 Compound 354 0.014 Compound 355 0.025 Compound 356 0.051 Compound 357 0.011 Compound 358 0.028 Compound 359 0.016 Compound 361a 0.015 Compound 361b 0.10 Compound 362 0.035 Compound 364 0.0051 Compound 365 0.013 Compound 367a 0.0039 Compound 367b 0.0048 Compound 368a 0.0030 Compound 368b 0.0035 Compound 369 0.0071 Compound 371a 0.030 Compound 371b 0.040 Compound 372a 0.037 Compound 372b 0.035 Compound 373a 0.20 Compound 373b 0.17 Compound 1′ 2.6 Compound 2′ 0.92
TABLE-US-00019 TABLE 10 Summary of kinetic assay data k.sub.on k.sub.off disc. t.sub.1/2 K.sub.I Compound (nM.sup.−1h.sup.−1).sup.a (h−.sup.1).sup.b (h).sup.c (nM).sup.d Compound 19 0.051 0.096 7.2 1.8 Compound 22 0.038 0.018 38 0.55 Compound 24b 0.052 0.015 45 0.29 Compound 24a 0.080 0.043 16 0.54 Compound 70 0.036 0.23 3.0 6.5 Compound 129 0.044 0.28 2.5 6.3 Compound 134 0.054 0.018 40 0.34 Compound 140a 0.047 0.024 29 0.50 Compound 140b 0.058 0.080 8.7 1.4 Compound 144 0.015 0.14 5.2 9.3 Compound 148 0.049 0.014 48 0.29 Compound 151 0.096 0.011 61 0.12 Compound 155 0.11 0.11 6.5 2.0 Compound 159 0.026 0.022 32 0.83 Compound 160 0.038 0.021 33 0.54 Compound 162a 0.029 0.055 13 1.9 Compound 165a 0.043 0.18 3.8 4.2 Compound 165b 0.043 0.17 4.2 3.9 Compound 182 0.11 0.029 24 0.26 Compound 192 0.052 0.033 21 0.64 Compound 229 0.061 0.018 39 0.29 Compound 223 0.023 0.088 7.9 0.26 Compound 237 0.082 0.036 19 0.44 (R)-Compound 239 0.060 0.086 8.1 1.4 Compound 257 0.066 0.067 10 0.96 Compound 262 0.032 0.103 6.7 0.31 Compound 269 0.020 0.080 8.7 4.0 Compound 297 0.037 0.014 49 0.38 Compound 298 0.071 0.027 26 0.38 Compound 305a 0.35 1.3 0.56 3.5 Compound 305b 0.38 1.4 0.49 3.7 Compound 317a 0.033 0.33 2.1 10 Compound 317b 0.059 0.35 2.0 5.9 Compound 320 0.027 0.015 45 0.57 Compound 322 0.037 0.12 5.7 3.3 Compound 333a 0.028 0.013 53 0.47 Compound 333b 0.014 0.011 63 0.77 Compound 351a 0.070 0.41 1.7 5.8 Compound 352a 0.10 0.38 1.8 3.7 Compound 352b 0.080 0.25 2.8 3.1 .sup.aon-rate from binding kinetics assay, .sup.boff-rate from binding kinetics assay, .sup.cdissociation half-life ln(2)/k.sub.off. .sup.dK.sub.I determined from binding kinetic assay k.sub.off/k.sub.on
TABLE-US-00020 TABLE 11 Summary of cellular assay data HCC-15 JIMT-1 NIH-OVCAR3 Compound IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) Compound 4 2.1 Compound 10 2.2 Compound 18 0.16 Compound 19 0.092 Compound 20 0.025 Compound 21 0.055 Compound 22 0.011 0.0078 0.0097 Compound 24 0.023 Compound 24a 0.26 Compound 24b 0.032 Compound 26 0.069 Compound 27 0.14 Compound 28 0.024 Compound 29 0.33 Compound 30 3.5 2.3 1.43 Compound 43 0.49 Compound 70 0.59 Compound 134 0.0051 0.0040 0.0051 Compound 140 0.038 Compound 140a 0.010 Compound 140b 0.045 Compound 148 0.036 Compound 151 0.013 Compound 153 0.044 Compound 157 0.60 0.44 0.72 Compound 159 0.021 0.015 0.022 Compound 160 0.0075 0.0054 0.0080 Compound 163 0.14 0.12 0.19 Compound 165a 0.068 0.045 0.059 Compound 165b 0.046 0.038 0.057 Compound 168 0.028 Compound 172 0.032 Compound 182 0.015 Compound 192 0.51 0.50 0.41 Compound 223 0.021 0.015 0.020 Compound 229 0.011 0.011 0.013 Compound 257 0.021 0.012 0.021 Compound 287b 0.097 0.064 0.033 Compound 297 0.011 0.0098 0.010 Compound 305a 0.074 0.052 0.090 Compound 305b 0.060 0.040 0.069 Compound 309 0.012 0.0094 0.012 Compound 310 0.011 0.0079 0.0091 Compound 320 0.021 0.014 0.020 Compound 322 0.043 0.032 0.040 Compound 333a 0.022 0.024 0.017 Compound 352a 0.034 0.040 0.045 Compound 352b 0.019 0.019 0.027 Compound 355 0.094 0.12 0.11 Compound 2′ 2.6
Assessment of In Vivo Activity
[0531] OVCAR-3 (ATCC) tumor cells were maintained in vitro in RPMI-1640 medium supplemented with 20% fetal bovine serum, 0.01 mg/mL bovine insulin and 1% Anti-Anti at 37° C. in an atmosphere of 5% CO.sub.2 in air. HCC15 (DSMZ) tumor cells were maintained in vitro in RPMI 1640 medium supplemented with 10% fetal bovine serum and 1% Anti-Anti at 37° C. in an atmosphere of 5% CO.sub.2 in air.
[0532] The tumor cells were sub-cultured twice weekly. The cells growing in an exponential growth phase were harvested and counted for tumor inoculation.
[0533] Tumor cells (10×10.sup.6) in 0.2 mL of PBS mixed with Matrigel (50:50) were inoculated subcutaneously on the right flank of each mouse. When the average tumor volume reached 110-175 mm.sup.3, animals were randomized into groups of 10 and treatment started. OVCAR-3 cells were implanted in Balb/C nude mice, and HCC15 cell were implanted in SCID Beige mice.
[0534] Compounds were dosed once or twice a day (12 h) orally. Tumor Growth Inhibition (TGI) was calculated using the formula: TGI (%)=[1−(T.sub.N−T.sub.0)/(V.sub.N−V.sub.0)]×100; T.sub.N is the average tumor volume of a treatment group at the indicated timepoint, T.sub.0 is the average tumor volume of the treatment group on treatment day 0, V.sub.N is the average tumor volume of the vehicle control group at the indicated timepoint, and V.sub.0 is the average tumor volume of the vehicle group on treatment day 0. P value was calculated based on tumor size by One-Way ANOVA with GraphPad Prism 9.4.0 compared with the vehicle group, respectively. **** indicates p<0.0001.
[0535] The tumor volume of vehicle- and compound-treated mice as a function of time after start of treatment and the results of treatments with selected compounds on SCID Beige mice or nude mice implanted with HCC15 or OVCAR-3 are shown in
TABLE-US-00021 TABLE 12 Compound Model Subfigure Dose TGI Compound 22 HCC15 1A 10 mg/kg BID PO 30 ± 15% Compound 22 HCC15 1A 30 mg/kg BID PO 72 ± 6% Compound 22 HCC15 1A 60 mg/kg BID PO 82 ± 9% Compound 22 OVCAR3 1B 10 mg/kg QD PO 24 ± 26% Compound 22 OVCAR3 1B 30 mg/kg QD PO 72 ± 17% Compound 22 OVCAR3 1B 60 mg/kg QD PO 82 ± 10% Compound 134 HCC15 1C 10 mg/kg BID PO 61 ± 10% Compound 134 HCC15 1C 30 mg/kg BID PO 89 ± 7% Compound 134 HCC15 1C 60 mg/kg BID PO 94 ± 5% Compound 134 OVCAR3 ID 10 mg/kg BID PO 60 ± 17% Compound 134 OVCAR3 1D 30 mg/kg BID PO 111 ± 1% Compound 134 OVCAR3 1D 60 mg/kg BID PO 112 ± 1% Compound 134 OVCAR3 1E 30 mg/kg QD PO 104 ± 7% Compound 134 OVCAR3 1E 60 mg/kg QD PO 109 ± 2% Compound 134 OVCAR3 1R 30 mg/kg BID PO 110 ± 1%