CYCLOALKYLUREA DERIVATIVE

Abstract

The present invention relates to a medicament for treating or preventing a disease related to orexin receptor, especially orexin type 2 receptor, comprising a new compound having a urea structure or a pharmaceutically acceptable salt thereof as an active ingredient. In more detail, the present invention relates to a medicament for treating or preventing narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea syndrome, etc.

Claims

1. A compound of formula (1): ##STR00751## or a pharmaceutically acceptable salt thereof wherein R.sup.1 is optionally-substituted C.sub.6-10 aromatic carbocyclyl group, optionally-substituted 5- to 10-membered aromatic heterocyclyl group, optionally-substituted C.sub.3-6 saturated carbocyclyl group, optionally-substituted 4- to 10-membered saturated heterocyclyl group, or cyano; L.sup.1 and L.sup.2 are each independently single bond, methylene (which may be optionally substituted with the same or different one or more C.sub.1-4 alky), —NR.sup.8—, —C(═O)—, —OC(═O)—, —SO—, —SO.sub.2—, —S—, or oxygen atom; R.sup.2 is hydrogen atom, hydroxy group, halogen atom, cyano, or optionally-substituted C.sub.1-4 alkyl; or when L.sup.1 is single bond, R.sup.1 and R.sup.2 may be combined together as a Spiro ring to form optionally-substituted C.sub.3-6 saturated carbocyclic ring or optionally-substituted 4- to 10-membered saturated heteroring; R.sup.3 and R.sup.4 are each independently hydrogen atom, halogen atom, cyano, —(C═O)NR.sup.5R.sup.6, carboxy group, —(C═O)O—R.sup.7, optionally-substituted C.sub.1-4 alkyl, or optionally-substituted C.sub.1-4 alkoxy, wherein R.sup.3 and R.sup.4 may bind to the same carbon atom if chemically possible; or when R.sup.3 and R.sup.4 bind to different ring carbon atoms, R.sup.3 and R.sup.4 may be taken together via C.sub.1-6 alkylene to form a fused ring or a bridged ring; R.sup.5 to R.sup.7 are each independently hydrogen atom, halogen atom, or optionally-substituted C.sub.1-4 alkyl; R.sup.8 is each independently hydrogen atom or optionally-substituted C.sub.1-4 alkyl; n is an integer of 1, 2, 3, or 4; Ring G is optionally-substituted C.sub.6-10 aromatic carbocyclyl group, optionally-substituted 5- to 10-membered aromatic heterocyclyl group, optionally-substituted C.sub.3-6 saturated carbocyclyl group, or optionally-substituted 4- to 10-membered saturated heterocyclyl group; A.sup.1 is oxygen atom or sulfur atom; A.sup.2 is oxygen atom or —NR.sup.8—, A.sup.3 is —CH—, nitrogen atom, or carbon atom; and the bond accompanied with broken line is each independently single bond or double bond.

2. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein in R.sup.2-R.sup.8, the optional substituent of “optionally-substituted C.sub.1-4 alkyl” is the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkoxy, C.sub.6-10 aromatic carbocyclyl group, and C.sub.3-7 cycloalkyl; and the optional substituent of “optionally-substituted C.sub.1-4 alkoxy” is the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.3-7 cycloalkyl; in R.sup.1, the optional substituent of “optionally-substituted C.sub.6-10 aromatic carbocyclyl group”, “optionally-substituted 5- to 10-membered aromatic heterocyclyl group”, “optionally-substituted C.sub.3-6 saturated carbocyclyl group”, and “optionally-substituted 4- to 10-membered saturated heterocyclyl group” is each independently at least one substituent selected from the group consisting of hydrogen atom, halogen atom, hydroxy group, C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), C.sub.1-6 alkylamino (the alkyl group of which may be optionally substituted with halogen atom, hydroxy group, or C.sub.3-7 cycloalkyl), C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), cyano, C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl optionally-substituted with the same or different one or more halogen atoms, and C.sub.3-7 cycloalkyl), and 5- to 10-membered aromatic heterocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl); and in Ring G, the optional substituent of “optionally-substituted C.sub.6-10 aromatic carbocyclyl group”, “optionally-substituted 5- to 10-membered aromatic heterocyclyl group”, “optionally-substituted C.sub.3-6 saturated carbocyclyl group”, and “optionally-substituted 4- to 10-membered saturated heterocyclyl group” is each independently at least one substituent selected from the group consisting of halogen atom, C.sub.1-6 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.3-7 cycloalkyl), C.sub.1-6 alkylamino (the alkyl group of which may be optionally substituted with halogen atom, hydroxy group, or C.sub.3-7 cycloalkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), and C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl); or when there are plural optional substituents, two of them may be taken together via C.sub.1-6 alkylene to form a chemically-possible bicyclic structure selected from a fused ring, a Spiro ring, and bridged ring.

3. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein in R.sup.2-R.sup.7, the optional substituent of “optionally-substituted C.sub.1-4 alkyl” is the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy; and the optional substituent of “optionally-substituted C.sub.1-4 alkoxy” is the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl; in R.sup.1, the optional substituent of “optionally-substituted C.sub.6-10 aromatic carbocyclyl group”, “optionally-substituted 5- to 10-membered aromatic heterocyclyl group”, “optionally-substituted C.sub.3-6 saturated carbocyclyl group”, and “optionally-substituted 4- to 10-membered saturated heterocyclyl group” is each independently at least one substituent selected from the group consisting of hydrogen atom, halogen atom, hydroxy group, C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), cyano, C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl optionally-substituted with the same or different one or more halogen atoms, and C.sub.3-7 cycloalkyl), and 5- to 10-membered aromatic heterocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl); and in Ring G, the optional substituent of “optionally-substituted C.sub.6-10 aromatic carbocyclyl group”, “optionally-substituted 5- to 10-membered aromatic heterocyclyl group”, “optionally-substituted C.sub.3-6 saturated carbocyclyl group”, and “optionally-substituted 4- to 10-membered saturated heterocyclyl group” is each independently at least one substituent selected from the group consisting of halogen atom, C.sub.1-6 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy), C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-6 alkylamino (the alkyl group of which may be optionally substituted with halogen atom, hydroxy group, or C.sub.3-7 cycloalkyl), and C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); or when there are plural optional substituents, two of them may be taken together via C.sub.1-6 alkylene to form a chemically-possible bicyclic structure selected from a fused ring, a spiro ring, and bridged ring.

4. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is selected from the following formulae (1a-1) to (1a-4): ##STR00752## wherein X.sup.1-X.sup.7 are each independently nitrogen atom or CR.sup.a6; Q.sup.1 and Q.sup.2 are oxygen atom, —NR.sup.a7—, or sulfur atom; R.sup.a1-R.sup.a7 are each independently (if there are plural CR.sup.a6, each R.sup.a6 is also independently), hydrogen atom, halogen atom, C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), cyano, C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or 5- to 10-membered aromatic heterocyclyl group; wherein R.sup.a4 and R.sup.a5 may bind to the same carbon atom if chemically possible; and when X.sup.1 and X.sup.3 are both CR.sup.a6, the two R.sup.a6 may be taken together with the carbon atoms to which they are each attached to form 6-membered carbon ring that is fused with the 5-membered ring comprising X.sup.1, X.sup.2, and X.sup.3; and q.sup.1 is an integer of 1 or 2.

5. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein Ring G is selected from the following (1b-1) to (1b-14): ##STR00753## ##STR00754## wherein W.sup.1, W.sup.3, W.sup.5, W.sup.6, W.sup.7, W.sup.11, W.sup.12, W.sup.13, W.sup.15, W.sup.16, W.sup.17, W.sup.19, and W.sup.25 are each independently nitrogen atom or CR.sup.b4, W.sup.2, W.sup.4, W.sup.8, W.sup.9, W.sup.10, W.sup.14, W.sup.18, W.sup.20, W.sup.21, W.sup.22, W.sup.23, and W.sup.24 are NR.sup.b5, oxygen atom, or CR.sup.b6R.sup.b7; R.sup.b1-R.sup.b7 are each independently (if there are plural CR.sup.b4, each R.sup.b4 is also independently), hydrogen atom, —N(R.sup.b8)R.sup.b9, C.sub.1-6 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.3-7 cycloalkyl which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl (said C.sub.1-4 alkyl may be substituted with halogen atom), and C.sub.1-4 alkoxy), C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), 5- to 10-membered aromatic heterocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); wherein R.sup.b1 and R.sup.b2 may bind to the same carbon atom if chemically possible; or R.sup.b1 and R.sup.b2 may be taken together via C.sub.1-6 alkylene to form a chemically-possible bicyclic structure selected from a fused ring, a Spiro ring, and bridged ring; and R.sup.b8 and R.sup.b9 are each independently hydrogen atom, C.sub.1-6 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkoxy, C.sub.3-7 cycloalkyl which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl (said C.sub.1-4 alkyl may be substituted with halogen atom), and 5- to 10-membered aromatic heterocyclyl group), C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl), 5- to 10-membered aromatic heterocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); or R.sup.b8 and R.sup.b9 may be taken together with the nitrogen atom to which they are attached to form 3- to 7-membered nitrogen-containing saturated heterocycle.

6. The compound of claim 1 of formula (2): ##STR00755## or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is selected from the following formulae (1a-1) to (1a-4): ##STR00756## wherein X.sup.1-X.sup.7 are each independently nitrogen atom or CR.sup.a6; Q.sup.1 and Q.sup.2 are oxygen atom, —NR.sup.a7—, or sulfur atom; R.sup.a1-R.sup.a7 are each independently (if there are plural CR.sup.a6, each R.sup.a6 is also independently), hydrogen atom, halogen atom, C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.3-6 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), cyano, C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or 5- to 10-membered aromatic heterocyclyl group; wherein R.sup.a4 and R.sup.a5 may bind to the same carbon atom if chemically possible; and when X.sup.1 and X.sup.3 are both CR.sup.a6, the two R.sup.a6 may be taken together with the carbon atoms to which they are each attached to form 6-membered carbon ring that is fused with the 5-membered ring comprising X.sup.1, X.sup.2, and X.sup.3; and q.sup.1 is an integer of 1 or 2; L.sup.1 and L.sup.2 are each independently single bond, —CH.sub.2—, or oxygen atom; R.sup.2 is hydrogen atom, hydroxy group, halogen atom, cyano, or optionally-substituted C.sub.1-4 alkyl; R.sup.3 and R.sup.4 are each independently hydrogen atom, halogen atom, C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkoxy, and C.sub.3-7 cycloalkyl), or C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.3-7 cycloalkyl); wherein R.sup.3 and R.sup.4 may bind to the same carbon atom if chemically possible; and when R.sup.3 and R.sup.4 bind to different carbon atoms on the ring, R.sup.3 and R.sup.4 may be taken together via C.sub.1-6 alkylene to form a fused ring or bridged ring; Ring G is selected from the following (1b-1) to (1b-4): ##STR00757## wherein W.sup.3, W.sup.5, W.sup.6, and W.sup.7 are each independently nitrogen atom or CR.sup.b4; W.sup.2, W.sup.4, and W.sup.8 are NR.sup.b5, oxygen atom or CR.sup.b6R.sup.b7; R.sup.b1-R.sup.b7 are each independently (if there are plural CR.sup.b4, each R.sup.b4 is also independently), hydrogen atom, C.sub.1-6 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy), C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); wherein R.sup.b1 and R.sup.b2 may bind to the same carbon atom if chemically possible; or R.sup.b1 and R.sup.b2 may be taken together via C.sub.1-6 alkylene to form a chemically-possible bicyclic structure selected from a fused ring, a Spiro ring, and bridged ring; A.sup.1 is oxygen atom or sulfur atom; A.sup.2 is oxygen atom or —NH—; and A.sup.3 is —CH—, nitrogen atom, or carbon atom.

7. The compound of claim 6 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is selected from the following formulae (1a-1), (1a-2), and (1a-3-1) ##STR00758## wherein X.sup.1-X.sup.6 are each independently nitrogen atom or CR.sup.a6; Q.sup.1 and Q.sup.2 are oxygen atom, —NR.sup.a7—, or sulfur atom; and R.sup.a1-R.sup.a3, R.sup.a6, and R.sup.a7 are each independently (if there are plural CR.sup.a6, each R.sup.a6 is also independently), hydrogen atom, halogen atom, C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), cyano, C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or 5- to 10-membered aromatic heterocyclyl group; wherein when X.sup.1 and X.sup.3 are both CR.sup.a6, the two R.sup.a6 may be taken together with the carbon atoms to which they are each attached to form 6-membered carbon ring that is fused with the 5-membered ring comprising X.sup.1, X.sup.2, and X.sup.3.

8. The compound of claim 6 or a pharmaceutically acceptable salt thereof, wherein Ring G is selected from the following (1b-1), (1b-2), and (1b-4): ##STR00759## wherein W.sup.1, W.sup.3, W.sup.5, W.sup.6, and W.sup.7 are each independently nitrogen atom or CR.sup.b4; W.sup.2 and W.sup.4 are NR.sup.b5 or CR.sup.b6R.sup.b7; and R.sup.b1, R.sup.b2, and R.sup.b4-R.sup.b7 are each independently (if there are plural CR.sup.b4, each R.sup.b4 is also independently), hydrogen atom, C.sub.1-6 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy), C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); or R.sup.b1 and R.sup.b2 may bind to the same carbon atom if chemically possible; or R.sup.b1 and R.sup.b2 may be taken together via C.sub.1-6 alkylene to form a bridged bicyclic structure.

9. The compound of claim 6 or a pharmaceutically acceptable salt thereof, wherein Ring G is selected from the following (1b-1) and (1b-2): ##STR00760## wherein W.sup.1 and W.sup.3 are nitrogen atom or CR.sup.b4; W.sup.2 and W.sup.4 are NR.sup.b5 or CR.sup.b6R.sup.b7; and R.sup.b1, R.sup.b2, and R.sup.b4-R.sup.b7 are each independently hydrogen atom, C.sub.1-6 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy), C.sub.6-10 aromatic carbocyclyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or C.sub.3-7 cycloalkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); wherein R.sup.b1 and R.sup.b2 may bind to the same carbon atom if chemically possible; or R.sup.b1 and R.sup.b2 may be taken together via C.sub.1-6 alkylene to form a bridged bicyclic structure.

10. The compound of claim 1 of formula (3): ##STR00761## or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is the following formula (1a-1), (1a-2), or (1a-3-1): ##STR00762## wherein X.sup.1-X.sup.6 are each independently nitrogen atom or CR.sup.a6; Q.sup.1 and Q.sup.2 are oxygen atom or sulfur atom; R.sup.a1-R.sup.a3 and R.sup.a6 are each independently (if there are plural CR.sup.a6, each R.sup.a6 is also independently), hydrogen atom, halogen atom, C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, and C.sub.1-4 alkoxy), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), cyano, or C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); wherein when X.sup.1 and X.sup.3 are both CR.sup.a6, the two R.sup.a6 may be taken together with the carbon atoms to which they are each attached to form 6-membered carbon ring that is fused with the 5-membered ring comprising X.sup.1, X.sup.2, and X.sup.3; L.sup.1 and L.sup.2 are each independently single bond or oxygen atom; R.sup.2 is hydrogen atom, halogen atom, or C.sub.1-4 alkyl which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and hydroxy group; R.sup.3 and R.sup.4 are each independently halogen atom; Ring G is the following (1b-1), (1b-2-1), (1b-2-2), or (1b-2-3): ##STR00763## wherein R.sup.b5 is hydrogen atom, or C.sub.1-6 alkyl which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy; and A.sup.1 is oxygen atom or sulfur atom.

11. The compound of claim 4 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is formula (1a-2), and R.sup.a1 is hydrogen atom, halogen atom, C.sub.1-4 alkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy), C.sub.3-7 cycloalkyl (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, hydroxy group, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy), or C.sub.1-4 alkoxy (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkyl).

12. The compound of claim 10 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is formula (1a-2), and X.sup.4 and X.sup.5 are both nitrogen atom.

13. The compound of claim 10 or a pharmaceutically acceptable salt thereof, wherein Ring G is formula (1b-1-1), and R.sup.b5 is C.sub.1-4 alkyl which may be optionally substituted with the same or different one or more halogen atoms.

14. The compound of claim 10 or a pharmaceutically acceptable salt thereof, wherein Ring G is formula (1b-2-1), and R.sup.b5 is hydrogen atom, or C.sub.1-4 alkyl which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy.

15. The compound of any one of claim 1 of formula (4): ##STR00764## or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is the following (1a-2-1): ##STR00765## wherein Q.sup.2 is oxygen atom or sulfur atom; R.sup.a2 is C.sub.3-7 cycloalkyl group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy) or cycloalkoxy group (which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom, C.sub.1-4 alkyl, and C.sub.1-4 alkoxy); R.sup.2 is C.sub.1-4 alkyl; Ring G is the following (1b-1-1) or (1b-2-1): ##STR00766## wherein R.sup.b5 is C.sub.1-4 alkyl which may be optionally substituted with the same or different one or more substituents selected from the group consisting of halogen atom and C.sub.1-4 alkoxy; and L.sup.2 is single bond or oxygen atom.

16. The compound of claim 15 or a pharmaceutically acceptable salt thereof, wherein R.sup.a2 is C.sub.3-7 cycloalkyl group which may be optionally substituted with the same or different one or more substituents selected from halogen atoms, and R.sup.2 is methyl group.

17. The compound of claim 15 or a pharmaceutically acceptable salt thereof, wherein R.sup.a2 is cyclopropyl group which may be optionally substituted with the same or different one or more substituents selected from halogen atoms, and R.sup.2 is methyl group.

18. The compound of claim 15 or a pharmaceutically acceptable salt thereof, wherein Ring G is formula (1b-2-1), and R.sup.b5 is isopropyl group.

19. The compound of claim 15 or a pharmaceutically acceptable salt thereof, wherein Ring G is formula (1b-1-1), and R.sup.b5 is isobutyl group.

20. The compound of claim 15 or a pharmaceutically acceptable salt thereof, wherein Ring G is formula (1b-1-1), R.sup.b5 is isopropyl group, and L.sup.2 is oxygen atom.

21. The compound of claim 15 or a pharmaceutically acceptable salt thereof, wherein Q.sup.2 is oxygen atom.

22. The compound of claim 1 or a pharmaceutically acceptable salt thereof, which is selected from the following compound names or structures: 4-(5-cyclopropyl-1,2-oxazol-3-yl)-N-{1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00767## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00768## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00769## 4-(5-cyclopropyl-1,2-oxazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00770## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[3-(propan-2-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00771## N-{(1R,6S)-2,2-difluoro-6-[3-(propan-2-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl]cyclohexyl}-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide ##STR00772## 4-(5-cyclopropyl-1,2-oxazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[3-(propan-2-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00773## N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00774## N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-{5-[(1S,2R)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide ##STR00775## N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-{5-[(1S,2R)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide ##STR00776## rac-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carbothioamide ##STR00777## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carbothioamide ##STR00778##

23. The compound of claim 1 or a pharmaceutically acceptable salt thereof, which is selected from the following compound names or structures: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00779## N-[(1R,6S)-2,2-difluoro-6-{[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide ##STR00780## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00781## N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00782## N-[(1R,6S)-2,2-difluoro-6-{[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00783## N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methyl-4-{5-[(1R,2S)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide ##STR00784## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S,4S)-4-fluoro-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00785## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-6-{[(3R)-4,4-difluoro-1-(propan-2-yl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-methylpiperidine-1-carboxamide. ##STR00786##

24. The compound of claim 1 or a pharmaceutically acceptable salt thereof, which is selected from the following compound names or structures: N-{(1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1R,2R)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00787## N-[(1R,6S)-2,2-difluoro-6-{methyl[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]amino}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00788## N-[(1R,6S)-2,2-difluoro-6-{(3S)-3-[methyl(propan-2-yl)amino]pyrrolidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00789## 4-(5-cyclobutyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00790## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{(3S)-3-[methyl(propan-2-yl)amino]pyrrolidin-1-yl}cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00791## N-{(1R,6S)-2,2-difluoro-6-[(2S)-2-methyl-4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00792## N-{(1R,6S)-2,2-difluoro-6-[(2R)-2-methyl-4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00793## N-[(1R,6S)-2,2-difluoro-6-{(3R)-3-[methyl(propan-2-yl)amino]pyrrolidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00794## N-[(1R,6S)-2,2-difluoro-6-{4-[methyl(propan-2-yl)amino]piperidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00795## N-[(1R,6S)-6-{(3S)-3-[cyclopropyl(methyl)amino]pyrrolidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00796## N-[(1R,6S)-2,2-difluoro-6-{(3S)-3-[methyl(2-methylpropyl)amino]pyrrolidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00797## N-[(1R,6S)-2,2-difluoro-6-(4-{methyl[(1-methylcyclopropyl)methyl]amino}piperidin-1-yl)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00798## N-[(1R,6S)-2,2-difluoro-6-(4-{[(1-fluorocyclopropyl)methyl](methyl)amino}piperidin-1-yl)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00799## N-[(1R,6S)-6-{(3S)-3-[(cyclopropylmethyl)(methyl)amino]pyrrolidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00800## N-[(1R,6S)-6-{(3S)-3-[(cyclopropylmethyl)(methyl)amino]pyrrolidin-1-yl}-2,2-difluorocyclohexyl]-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carboxamide ##STR00801## rac-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,2R,6S)-2-fluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00802## N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)-1,4-diazepan-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00803## 4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-N-{(1R,2S,6S)-2-fluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00804## 4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-N-{(1S,2R,6R)-2-fluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide ##STR00805## N-[(1R,6S)-2,2-difluoro-6-{4-[methyl(2-methylpropyl)amino]piperidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00806## N-[(1R,6S)-6-{4-[(cyclopropylmethyl)(methyl)amino]piperidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00807## N-[(1R,6S)-6-{4-[cyclobutyl(methyl)amino]piperidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00808## N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]amino}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00809##

25. The compound of claim 1 or a pharmaceutically acceptable salt thereof, which is selected from the following compound names or structures: N-[(1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)piperidin-4-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00810## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[1-(propan-2yl)piperidin-4-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00811## 4-(5-cyclobutyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00812## N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-ethyl-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide ##STR00813## N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00814## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00815## N-[(1R,6S)-6-{[(3S)-1-(cyclopropylmethyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00816## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-6-{[(3S)-1-(2,2-dimethylpropyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00817## N-[(1R,6S)-6-{[(3S)-1-(2,2-dimethylpropyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00818## N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-methylcyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00819## N-[(1R,6S)-6-{[(3S)-1-(cyclopropylmethyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carboxamide ##STR00820## 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-methylcyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-methylpiperidine-1-carboxamide ##STR00821## N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-fluorocyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00822## N-[(1R,6S)-2,2-di fluoro-6-(4-{methyl[(1-methylcyclopropyl)methyl]amino}piperidin-1-yl)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide ##STR00823## N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-fluoro-2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide. ##STR00824##

26-28. (canceled)

29. A method for treating narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea syndrome, narcolepsy syndrome involving narcolepsy-like symptom, hypersomnia associated with Parkinson's disease, or hypersomnia associated with dementia with Lewy body, comprising administering a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof to a patient in need thereof.

30. (canceled)

Description

DESCRIPTION OF EMBODIMENTS

[0334] Hereinafter, the present invention is explained in more detail. In the description, the number of carbon atoms in the definition of “substituents” can indicates, for example, “C.sub.1-6”. The specific definition “C.sub.1-6 alkyl” means an alkyl group having 1 to 6 carbon atoms. In the present description, a substituent group which is not accompanied with “optionally-substituted” or “substituted” means an “unsubstituted” substituent group. For example, “C.sub.1-6 alkyl” means “unsubstituted C.sub.1-6 alkyl”.

[0335] The substituent groups in the present description may be sometimes expressed without the term “group”. In case that “optionally-substituted” is used in the definition of substituent groups, the number of the substituting groups is not limited as long as the substitutions are available, i.e., it is one or more. It means that the possible number of substituting groups is the substitution-available number on carbon atoms or carbon/nitrogen atoms in a substituent group which are acceptable for substitution. Unless otherwise specified, the definition of each substituent group also extends over the case that the substituent group is partially included in another substituent group or the case that the substituent group is attached to another substituent group.

[0336] Unless otherwise specified, the binding site of substituent groups is not limited as long as the site is available to be bound.

[0337] The “halogen” includes, for example, fluorine, chlorine, bromine, iodine, and the like. It is preferably fluorine or chlorine.

[0338] The “C.sub.1-4 alkyl” means straight or branched chain saturated hydrocarbon group having 1 to 4 carbon atoms, and the “C.sub.1-6 alkyl” means straight or branched chain saturated hydrocarbon group having 1 to 6 carbon atoms. The “C.sub.1-4 alkyl” includes, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, and Cert-butyl, and the “C.sub.1-6 alkyl” includes, for example, pentyl, isopentyl, neopentyl, 1-ethylpropyl, hexyl, and a structural isomer thereof, besides the above C.sub.1-4 alkyl. Preferred examples of the “C.sub.1-6 alkyl” or “C.sub.1-4 alkyl” include methyl, ethyl, propyl, and isopropyl; more preferably methyl and isopropyl.

[0339] The “C.sub.1-6 alkylene” means divalent straight or branched chain saturated hydrocarbon group having 1 to 6 carbon atoms. The “C.sub.1-6 alkylene” includes preferably “C.sub.1-4 alkylene”, more preferably “C.sub.1-3 alkylene”. The “C.sub.1-3 alkylene” includes, for example, methylene, ethylene, propylene, trimethylene, and the like. The “C.sub.1-4 alkylene” includes, for example, butylene, 1,1-dimethylethylene, 1,2-dimethylethylene, 1-methyltrimethylene, 2-methyltrimethylene, and the like, besides the examples listed in the said “C.sub.1-3 alkylene”. The “C.sub.1-6 alkylene” includes, for example, pentylene, 1,1-dimethyltrimethylene, 1,2-dimethyltrimethylene, 1-methylbutylene, 2-methylbutylene, 1-methylpentylene, 2-methylpentylene, 3-methylpentylene, hexylene, and the like, besides the examples listed in the said “C.sub.1-4 alkylene”.

[0340] The “C.sub.3-7 cycloalkyl” means a non-aromatic cyclic hydrocarbon group (i.e., saturated hydrocarbon group and partially-unsaturated hydrocarbon group) having 3 to 7 carbon atoms, which includes preferably “C.sub.3-6 cycloalkyl”. The “C.sub.3-7 cycloalkyl” also includes a bridged one. The “C.sub.3-10 cycloalkyl” includes, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentenyl, cyclohexenyl, and cycloheptyl.

[0341] The “C.sub.3-7 cycloalkyl” also includes a bi-cyclic condensed ring in which the “C.sub.3-7 cycloalkyl” is fused with benzene or a 5- or 6-membered ring having one heteroatom selected from nitrogen, sulfur, or oxygen atom, or the same or different and two or more (for example, 2 to 4) heteroatoms thereof (for example, “5- or 6-membered monocyclic heteroaryl” mentioned below, and 5- or 6-membered ring in “4- to 10-membered saturated heterocyclyl” mentioned below).

[0342] The “C.sub.1-4 alkoxy” means oxy group substituted with the above “C.sub.1-4 alkyl”, and the “C.sub.1-6 alkoxy” means oxy group substituted with the above “C.sub.1-6 alkyl”. The “C.sub.1-4 alkoxy” includes, for example, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, and Cert-butoxy. Preferably, the “C.sub.1-4 alkoxy” includes methoxy, ethoxy, and isopropoxy.

[0343] The “C.sub.3-7 cycloalkoxy” means oxy group substituted with the above “C.sub.3-7 cycloalkyl”, which includes preferably “C.sub.3-6 cycloalkoxy”. The “C.sub.3-7 cycloalkoxy” includes, for example, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, and cyclohexyloxy, and preferably cyclohexyloxy.

[0344] The “C.sub.6-10 aromatic carbocyclyl group” means an aromatic hydrocarbon group having 6 to 10 carbon atoms, which is also referred to as “C.sub.6-10 aryl”. More preferably, it is phenyl. The “C.sub.6-10 aromatic carbocyclyl group” includes, for example, phenyl, 1-naphthyl, and 2-naphthyl.

[0345] The “C.sub.6-10 aromatic carbocyclyl group” also includes a condensed ring in which “phenyl” is fused with a 5- or 6-membered ring having one heteroatom selected from nitrogen, sulfur, or oxygen atom, or the same or different and two or more (for example, 2 to 4) heteroatoms thereof (for example, “5- or 6-membered monocyclic aromatic heterocyclyl group” mentioned below, and 5- or 6-membered ring in “4- to 10-membered saturated heterocyclyl” mentioned below), or a 5- to 7-membered cycloalkyl ring (for example, cyclopentane, cyclohexane and cycloheptane).

[0346] The “5- to 10-membered aromatic heterocyclyl group” means a 5- to 10-membered mono- or multiple-cyclic aromatic group having one heteroatom selected from nitrogen, sulfur, or oxygen atom, or the same or different and two or more (for example, 2 to 4) heteroatoms thereof, besides carbon atoms as the ring atoms, preferably, “5- or 6-membered monocyclic aromatic heterocyclyl group”. The “5- or 6-membered monocyclic aromatic heterocyclyl group” means a 5- or 6-membered monocyclic aromatic group within the “5- to 10-membered aromatic heterocyclyl group”.

[0347] The multiple-cyclic aromatic heterocyclyl group in the “5- to 10-membered aromatic heterocyclyl group” includes, for example, a condensed ring in which the same or different two monocyclic aromatic heterorings are fused, or a monocyclic aromatic heteroring and an aromatic ring (for example, benzene) or a non-aromatic ring (for example, cyclohexane) are fused.

[0348] The “5- to 10-membered aromatic heterocyclyl group” includes, for example, pyrazolyl, imidazolyl, pyridyl, pyrimidinyl, pyrazinyl, and pyridazinyl. Another embodiment includes, preferably, benzofuranyl in which the binding site is on the heteroaryl (furan) ring, pyridyl, pyrimidinyl, pyrazinyl, and pyridazinyl.

[0349] The “C.sub.3-6 saturated carbocyclic ring” means a monocyclic saturated or partially-unsaturated hydrocarbon ring having 3 to 6 carbon atoms. The “C.sub.3-6 saturated carbocyclic ring” includes, for example, cyclopropane, cyclobutane, cyclopentane, cyclohexane, cyclopropene, cyclobutane, cyclopentene, cyclohexene, and cyclohexadiene, and preferably cyclopropane and cyclobutane.

[0350] The “4- to 10-membered saturated heteroring” means a monocyclic or bicyclic saturated heteroring composed of 4 to 10 atoms, which has the same or different and one or more (for example, 2 to 4, preferably 2 to 3, more preferably 2) heteroatoms selected from oxygen atom, nitrogen atom, and sulfur atom, besides carbon atoms as the ring atoms. The heteroring may include a partially-unsaturated one, a partially-bridged one, and a partially-spiro one. Preferred one thereof is a 5- or 6-membered saturated heteroring. The bicyclic saturated heteroring also includes a condensed ring of a monocyclic saturated heteroring, and benzene or a 5- or 6-membered monocyclic aromatic heteroring. And, the saturated heteroring may further comprise one or two carbonyl, thiocarbonyl, sulfinyl, or sulfonyl, that is, the saturated heteroring includes, for example, a cyclic group such as lactam, thiolactam, lactone, thiolactone, cyclic imide, cyclic carbamate, and cyclic thiocarbamate, wherein the number of atoms composing 4- to 10-membered ring (i.e., ring size) or the number of heteroatoms composing hetero ring does not count the oxygen atom in carbonyl, sulfinyl, and sulfonyl, and the sulfur atom in thiocarbonyl. The “4-to 10-membered saturated heteroring” includes preferably monocyclic or bicyclic “4- to 8-membered saturated heteroring”, more preferably monocyclic “4- to 6-membered saturated heteroring”, and even more preferably monocyclic “5- or 6-membered saturated heteroring”. The “4- to 10-membered saturated heteroring” includes, for example, piperazine, oxetanyl, azetidinyl, pyranyl, tetrahydrofuryl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, piperidinyl, morpholinyl, homopiperidinyl, oxetanyl, thiomorpholinyl, dioxothiomorpholinyl, hexamethyleneiminyl, oxazolidinyl, thiazolidinyl, imidazolidinyl, oxoimidazolidinyl, dioxoimidazolidinyl, oxooxazolidinyl, dioxooxazolidinyl, dioxothiazolidinyl, tetrahydrofuranyl, tetrahydropyranyl, and tetrahydropyridinyl, and preferably pyranyl, tetrahydrofuryl, pyrrolidinyl, piperidinyl, piperazinyl, and morpholinyl. The “bicyclic saturated heteroring” includes, for example, dihydroindolyl, dihydroisoindolyl, dihydropurinyl, dihydrothiazolopyrimidinyl, dihydrobenzodioxanyl, isoindolinyl, indazolyl, pyrrolopyridinyl, tetrahydroquinolinyl, decahydroquinolinyl, tetrahydroisoquinolinyl, decahydroisoquinolinyl, tetrahydronaphthyridinyl, and tetrahydropyrido-azepinyl.

[0351] The “4- to 6-membered saturated heterocyclyl group” means a monovalent substituent derived from “4- to 6-membered saturated heteroring” which belongs to the above “4- to 10-membered saturated heteroring”. It includes preferably azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, oxetanyl, tetrahydrofuranyl, and tetrahydropyranyl.

[0352] The “3- to 7-membered nitrogen-containing saturated heterocycle” which is formed by taking together R.sup.b8 and R.sup.b9 with the nitrogen atom to which they are attached corresponds to the above “4- to 10-membered saturated heteroring” wherein the number of atoms composing the ring is 3 to 7, and one nitrogen atom is included as an atom composing the ring besides carbon atoms.

[0353] The compound of the present invention includes various hydrate, solvate, and crystal polymorph thereof.

[0354] The compound of the present invention may include one or more isotope atoms such as D, .sup.3H, .sup.11C, .sup.13C, .sup.14C, .sup.13N, .sup.15N, .sup.15O, .sup.35S, .sup.18F, and .sup.125I by substitution, and such isotope-substituted compound is also included in the compound of the present invention.

[0355] The “pharmaceutically acceptable salt” used herein means a pharmaceutically usable acid addition salt and a pharmaceutically usable base addition salt. The “pharmaceutically acceptable salt” includes, but not limited thereto, for example, an acid addition salt such as acetate, propionate, butyrate, formate, trifluoroacetate, maleate, fumarate, tartrate, citrate, stearate, succinate, ethylsuccinate, malonate, lactobionate, gluconate, glucoheptonate, benzoate, methanesulfonate, benzenesulfonate, p-toluenesulfonate (tosylate), laurylsulfate, malate, ascorbate, mandelate, saccharin, xinafoate, pamoate, cinnamate, adipate, cysteine, N-acetylcysteine, hydrochloride, hydrobromide, phosphate, sulfate, hydroiodide, nicotinate, oxalate, picrate, thiocyanate, undecanoate, polyacrylate, and carboxy vinyl polymer; an inorganic base addition salt such as lithium salt, sodium salt, potassium salt, and calcium salt; an organic base addition salt such as morpholine and piperidine; and amino acid addition salt such as aspartate and glutamate.

[0356] The present compounds can be orally or parenterally administered directly or as a suitable formulation such as drug product, medicament, and pharmaceutical composition. The formulation thereof may include, for example, tablet, capsule, powder, granule, liquid, suspension, injection, patch, gel patch, and the like, but not limited thereto. The formulation can be prepared with pharmaceutically acceptable additive agents in known means.

[0357] The additive agents can be chosen for any purpose, including an excipient, a disintegrant, a binder, a fluidizer, a lubricant, a coating agent, a solubilizer, a solubilizing agent, a thickener, dispersant, a stabilizing agent, a sweetening agent, a flavor, and the like. Specifically, they include, for example, lactose, mannitol, microcrystalline cellulose, low-substituted hydroxypropylcellulose, cornstarch, partially-pregelatinized starch, carmellose calcium, croscarmellose sodium, hydroxypropylcellulose, hydroxypropyl methylcellulose, polyvinyl alcohol, magnesium stearate, sodium stearyl fumarate, polyethylene glycol, propylene glycol, titanium oxide, talc, and the like.

[0358] The dose of the present compound should be suitably determined depending on subject animal for administration, administration route, target disease, and age, body weight, and condition of patients. For example, in the case of oral administration, about 0.01 mg as minimum to 10000 mg as maximum may be administered a day for an adult in one to several portions.

[0359] The compound of the present invention has agonist activity for orexin receptor. Thereby, the compound can be a medicament for preventing or treating a disease related to orexin receptor. The disease includes, for example, narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea syndrome, narcolepsy syndrome involving narcolepsy-like symptom, hypersomnia associated with Parkinson's disease, hypersomnia associated with dementia with Lewy body, hypersomnia syndrome involving daytime hypersomnia (e.g. Kleine-Levin syndrome, major depression accompanied by hypersomnia, dementia with Lewy body, Parkinson's disease, progressive supranuclear palsy, Prader-Willi syndrome, Moebius syndrome, hypoventilation syndrome, Niemann-Pick disease type C, brain contusion, cerebral infarction, brain tumor, muscular dystrophy, multiple sclerosis, acute disseminated encephalomyelitis, Guillain-Barre syndrome, Rasmussen's encephalitis, Wernicke's encephalopathy, limbic encephalitis, Hashimoto encephalopathy), coma, loss of consciousness, obesity (e.g. malignant mast cell, extrinsic obesity, hyperinsulinar obesity, hyperplasmic obesity, hypophysial obesity, hypoplasmic obesity, hypothyroid obesity, hypothalamic obesity, symptomatic obesity, childhood obesity, upper body obesity, alimentary obesity, gonadal obesity, systemic mastocytosis, primary obesity, central obesity), insulin resistance syndrome, Alzheimer, impaired consciousness such as coma, side effect or complication caused by anesthesia, sleep disturbance, sleep problem, insomnia, intermittent sleep, night myoclonus, REM sleep interruption, jet lag, jet lag syndrome, sleep disorder of shift workers, dyssomnia, sleep terror, depression, major depression, sleepwalking, enuresis, sleep disorder, Alzheimer's sundown syndrome, disease associated with circadian rhythm, fibromyalgia, condition resulting from decrease in sleeping quality, bulimia, obsessive eating disorder, obesity-related diseases, hypertension, diabetes, elevated plasma insulin level/insulin resistance, hyperlipemia, hyperlipidaemia, endometrial cancer, breast cancer, prostate cancer, colon cancer, cancer, osteoarthritis, obstructive sleep apnea, cholelithiasis, gallstone, heart disease, abnormal heartbeat, arrhythmia, myocardial infarction, congestive heart failure, heart failure, coronary heart disease, cardiovascular disease, sudden death, polycystic ovary, craniopharyngioma, Prader-Willi syndrome, Froehlich syndrome, growth hormone deficiency, normal variant short stature, Turner syndrome, children suffering from acute lymphoblastic leukemia, syndrome X, reproductive hormone abnormality, decrease of fecundability, infertility, hypogonadism in men, sexual/reproductive-function dysfunction such as hirsutism in women, fetal defect associated with maternity obesity, gastrointestinal motility disorder such as obesity-related gastroesophageal reflux, obesity hypoventilation syndrome (Pickwickian syndrome), respiratory disease such as respiratory distress, inflammation such as vascular systemic inflammation, arteriosclerosis, hypercholesterolemia, hyperuricemia, low back pain, gallbladder disease, gout, renal cancer, secondary risk of obesity such as risk of left ventricle hypertrophy, migraine, headache, neuropathic pain, Parkinson's disease, psychosis, schizophrenia, facial flushing, night sweat, disease in genitalium/urinary system, disease associated with sexual function or fecundability, dysthymic disorder, bipolar disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, acute stress disorder, agoraphobia, generalized anxiety disorder, obsessive-compulsive disorder, panic attack, panic disorder, posttraumatic stress disorder, separation anxiety disorder, social phobia, anxiety disorder, acute neurological and psychiatric disorder such as cerebral deficiency developed after heart bypass surgery or heart transplant, stroke, ischemic stroke, cerebral ischemia, spinal cord trauma, head injury, periparturient hypoxia, cardiac arrest, hypoglycemic nerve injury, Huntington's disease, amyotrophic lateral sclerosis, multiple sclerosis, eye damage, retinopathy, cognitive impairment, muscle spasm, tremor, epilepsy, disorder associated with muscle spasm, delirium, amnestic disorder, age-associated cognitive decline, schizoaffective disorder, paranoia, drug addiction, movement disorder, chronic fatigue syndrome, fatigue, medication-induced parkinsonian syndrome, Gilles de la Tourette syndrome, chorea, myoclonus, tic, restless legs syndrome, dystonia, dyskinesia, attention deficit hyperactivity disorder (ADHD), conduct disorder, urinary incontinence, withdrawal symptom, trigeminal neuralgia, hearing loss, tinnitus, nerve injury, retinopathy, macular degeneration, vomiting, cerebral edema, pain, bone pain, arthralgia, toothache, cataplexy, and traumatic brain injury; and preferably narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea syndrome, narcolepsy syndrome involving narcolepsy-like symptom, hypersomnia associated with Parkinson's disease, and hypersomnia associated with dementia with Lewy body.

[0360] Hereinafter, the processes to prepare the compound of the present invention of formula (1) are exemplified along with examples, but the processes of the present invention should not be limited to the examples.

Preparation Process

[0361] The compound of the present invention may be synthesized according to each Preparation Process shown below or its combination with a known synthetic process.

[0362] Each compound in the following schemes may exist as a salt thereof, wherein the salt includes, for example, the “pharmaceutically acceptable salt” mentioned above. The following schemes are disclosed as just examples, thus it is also possible to optionally prepare the present compound by a different process based on the knowledge of a skilled person in synthetic organic chemistry field.

[0363] In each Preparation Process described below, protecting groups can be used as necessary, even if the use of protecting groups is not explicitly stated. And, the protecting groups can be deprotected after a reaction is completed or a series of reactions have been carried out to obtain the desired compound.

[0364] As such protecting groups, for example, general protecting groups described in T. W. Greene, and P. G. M. Wuts, “Protective Groups in Organic Synthesis”, 3rd Ed., John Wiley & Sons, Inc., New York (1999), and the like may be used. Examples of amino-protecting groups include, for toluenesulfonyl, o-nitrobenzenesulfonyl, tetrahydropyranyl, and the like; examples of hydroxy-protecting groups include, for example, trialkylsilyl, acetyl, benzyl, tetrahydropyranyl, methoxymethyl, and the like; examples of aldehyde-protecting groups include, for example, dialkylacetal, cyclic alkylacetal, and the like; and examples of carboxyl-protecting groups include, for example, tert-butyl ester, orthoester, amide, and the like.

[0365] The introduction and elimination of protecting groups can be carried out by a method commonly-used in synthetic organic chemistry (for example, see T. W. Greene, and P. G. M. Wuts, “Protective Groups in Organic Synthesis”, 3rd Ed., John Wiley & Sons, Inc., New York (1999)), or a similar method.

Preparation Process 1:

[0366] In compounds according to formula (1) or a pharmaceutically acceptable salt thereof, the compound of formula (s-1-1) or a pharmaceutically acceptable salt thereof which is a compound of formula (1) wherein A.sup.3 is nitrogen atom can be prepared, for example, by the following process.

##STR00110##

wherein R.sup.1-R.sup.4, L.sup.1, L.sup.2, n, Ring G, A.sup.1, and the bond accompanied with broken line are as defined in Item 1.

Step (1-1):

[0367] Compound (s-1-1) can be prepared by reacting compound (s-1-2) and compound (s-1-3) in a suitable inert solvent under a reaction condition of urea-binding formulation. The present reaction condition includes, for example, using triphosgene, 4-nitrophenyl chloroformate, 1,1′-carbonyldiimidazole, or thiophosgene. A base is used in the present reaction, and the base used herein includes triethylamine and diisopropylethylamine. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

[0368] In Step (1-1), the intermediate such as an isocyanate may isolated, followed by transforming the intermediate.

Preparation Process 2:

[0369] In compounds according to formula (s-1-3), the compound of formula (s-2-1) which is a compound of formula (s-1-3) having no unsaturated bond in the ring can be prepared, for example, by the following process, provided that L.sup.2 is oxygen atom or —NR.sup.10—, or L.sup.2 is single bond and Ring G is connected to the cycloalkyl via a nitrogen atom therein, wherein R.sup.10 is H or C.sub.1-4 alkyl, said definition is used below unless otherwise indicated.

##STR00111##

wherein R.sup.3, R.sup.4, L.sup.2, n, and Ring G are as defined in Item 1; P.sup.1 is a suitable protecting group; and LG is a suitable leaving group, said definitions are used below unless otherwise indicated.

[0370] Compound (s-2-1) can be prepared from compound (s-2-2) via Step (2-1) and Step (2-2).

Step (2-1):

[0371] Compound (s-2-4) can be prepared by reacting compound (s-2-2) and compound (s-2-3) in a suitable inert solvent without additives or in the presence of a acid or a base. The acid used herein includes, for example, a protonic acid such as hydrochloric acid, sulfuric acid, phosphoric acid, methanesulfonic acid, benzenesulfonic acid, and p-toluenesulfonic; and a Lewis acid such as zinc(II) chloride, scandium(III) triflate, copper(I) chloride, boron trifluoride, boronic acid, and boronate ester. The base used herein includes, for example, an organic base such as triethylamine, diisopropylethylamine, and DBU; an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate; a metal alkoxide such as potassium tert-butoxide; an organometallic reagent such as n-butyl lithium and isopropylmagnesium chloride; and a metal amide reagent such as LDA and LHMDS. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (2-2):

[0372] Compound (s-2-1) can be prepared by reacting compound (s-2-4) in a suitable inert solvent or under hydrogen atmosphere as necessary, under a conventional condition of nitro-reduction. The present reaction condition includes, for example, using ferrum, zinc, tin(II) chloride, Raney nickel, palladium carbon, or palladium(II) hydroxide. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; an ester solvent such as ethyl acetate and methyl acetate; and an alcohol solvent such as methanol and ethanol. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

[0373] Compound (s-2-1) can be also prepared from compound (s-2-5) via Step (2-3) and Step (2-4).

Step (2-3):

[0374] Compound (s-2-6) can be prepared by reacting compound (s-2-5) and compound (s-2-3) in a suitable inert solvent without additives or in the presence of an acid or a base under a conventional condition of aziridine-ring-opening reaction. The acid used herein includes, for example, a protonic acid such as hydrochloric acid, sulfuric acid, phosphoric acid, methanesulfonic acid, benzenesulfonic acid, and p-toluenesulfonic; and a Lewis acid such as zinc(II) chloride, scandium(III) triflate, copper(I) chloride, boron trifluoride, boronic acid, and boronate ester. The base used herein includes, for example, an organic base such as triethylamine, diisopropylethylamine, and DBU; an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate; a metal alkoxide such as potassium tert-butoxide; an organometallic reagent such as n-butyl lithium and isopropylmagnesium chloride; and a metal amide reagent such as LDA and LHMDS. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (2-4):

[0375] Compound (s-2-1) can be prepared by deprotecting compound (s-2-6) in a known manner (for example, a manner described in Protective Groups in Organic Synthesis 3.sup.rd Edition (John Wiley & Sons, Inc.), Comprehensive Organic Transformation, edited by R. C. Larock, VCH publisher Inc., 1989, etc.) or a similar manner thereto.

[0376] Compound (s-2-1) can be also prepared from compound (s-2-7) via Step (2-5)-Step (2-7), and Step (2-4).

Step (2-5):

[0377] Compound (s-2-8) can be prepared by reacting compound (s-2-7) and compound (s-2-3) in a suitable inert solvent without additives or in the presence of a acid or a base under a conventional condition of epoxide-ring-opening reaction. The acid used herein includes, for example, a protonic acid such as hydrochloric acid, sulfuric acid, phosphoric acid, methanesulfonic acid, benzenesulfonic acid, and p-toluenesulfonic; and a Lewis acid such as boron trifluoride, zinc(II) chloride, scandium(III) triflate, copper(I) chloride, boronic acid, and boronate ester. The base used herein includes, for example, an organic base such as triethylamine, diisopropylethylamine, and DBU; an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate; a metal alkoxide such as potassium tert-butoxide; an organometallic reagent such as n-butyl lithium and isopropylmagnesium chloride; and a metal amide reagent such as LDA and LHMDS. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (2-6):

[0378] Compound (s-2-9) can be prepared by reacting compound (s-2-8) in a suitable inert solvent under a conventional condition of transformation reaction from hydroxy group to a leaving group. The present reaction condition includes, for example, using methanesulfonyl chloride, p-toluenesulfonyl chloride, or trifluoromethanesulfonyl chloride. A base is used in the present reaction, and the base used herein includes, for example, an organic base such as triethylamine, diisopropylethylamine, and DBU; an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate; a metal alkoxide such as potassium Cert-butoxide; an organometallic reagent such as n-butyl lithium and isopropylmagnesium chloride; and a metal amide reagent such as LDA and LHMDS. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (2-7):

[0379] Compound (s-2-6) can be prepared in a general nucleophilic substitution reaction with compound (s-2-9), P.sup.1NH.sub.2, and a base. The base used herein includes, for example, an organic base such as triethylamine, diisopropylethylamine, and DBU; an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate; a metal alkoxide such as potassium tert-butoxide; an organometallic reagent such as n-butyl lithium and isopropylmagnesium chloride; and a metal amide reagent such as LDA and LHMDS. The solvent used herein includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

[0380] Step (2-6) and Step (2-7) may be carried out as one step without isolating the intermediate. And, Step (2-6) and Step (2-7) may be also carried out as one step under Mitsunobu reaction condition.

Preparation Process 3-1:

[0381] In compounds according to formula (s-2-1), the compound of formula (s-3-1) which is a compound of formula (s-2-1) wherein L.sup.2 is single bond and Ring G binds to cycloalkyl via nitrogen atom therein can be also prepared, for example, by the following process.

##STR00112##

wherein R.sup.3, R.sup.4, n, and Ring G are as defined in Item 1.

[0382] Compound (s-3-1) can be prepared from compound (s-2-2) via Step (3-1)-Step (3-3).

Step (3-1):

[0383] Compound (s-3-2) can be prepared in a similar manner to Step (2-1) with compound (s-2-2) and ammonia or a reagent equal to ammonia that includes a protected-amine reagent which is deprotected after the amination and an azide-inducer which is reduced after the azidation.

Step (3-2):

[0384] Compound (s-3-3) can be prepared in a nitrogen-containing heteroring-formulation with compound (s-3-2). For example, compound (s-3-3) wherein Ring G is piperazine can be prepared by reacting compound (s-3-2) with N-benzyl-bis(2-chloroethyl)amine, followed by deprotection and alkylation.

Step (3-3):

[0385] Compound (s-3-1) can be prepared in a similar manner to Step (2-2) with compound (s-3-3).

[0386] Compound (s-3-1) can be also prepared from compound (s-2-5) via Step (3-4)-Step (3-6).

Step (3-4):

[0387] Compound (s-3-4) can be prepared in a similar manner to Step (2-3) with compound (s-2-5) and ammonia or a reagent equal to ammonia that includes a protected-amine reagent which is deprotected after the amination and an azide-inducer which is reduced after the azidation.

Step (3-5):

[0388] Compound (s-3-5) can be prepared in a similar manner to Step (3-2) with compound (s-3-4).

Step (3-6):

[0389] Compound (s-3-1) can be prepared in a similar deprotection to Step (2-4) with compound (s-3-5).

Preparation Process 3-2:

[0390] The compound according to formula (s-3-1) can be also prepared, for example, by the following process.

##STR00113##

wherein R.sup.3, R.sup.4, n, and Ring G are as defined in Item 1.

[0391] Compound (s-3-1) can be prepared from compound (s-3-6) via Step (3-7) and Step (3-8).

Step (3-7):

[0392] Compound (s-3-6) is compound (s-2-9) in Preparation Process 2, wherein L.sup.2 is single bond and Ring G is connected to the cycloalkyl via a nitrogen atom therein. Compound (s-3-7) can be prepared in a general nucleophilic substitution reaction like Step (2-7) with compound (s-3-6) and a conventional base as intramolecular reaction. Compound (s-3-7) may be used in the next step without isolation.

Step (3-8):

[0393] Compound (s-3-1) can be prepared in a general ring-opening reaction with compound (s-3-7) and ammonia or a reagent equal to ammonia that includes a protected-amine reagent which is deprotected after the amination and an azide-inducer which is reduced after the azidation.

Preparation Process 4:

[0394] In compounds according to formula (s-2-1), the compound of formula (s-4-1) which is a compound of formula (s-2-1) wherein L.sup.2 is O or NR.sup.10 can be also prepared, for example, by the following process.

##STR00114##

wherein R.sup.3, R.sup.4, n, and Ring G are as defined in Item 1; and Y is O or NR.sup.10, said definitions are used below unless otherwise indicated.

[0395] Compound (s-4-1) can be prepared from compound (s-2-2) via Step (4-1)-Step (4-3).

Step (4-1):

[0396] Compound (s-4-2) can be prepared by reacting compound (s-2-2) in a similar manner to Step (2-1) with YH.sub.2 or a reagent equal to YH.sub.2 that includes a protected reagent P.sup.2YH which is deprotected after the addition reaction, wherein P.sup.2 is a suitable protecting group, said definition is used below unless otherwise indicated.

Step (4-2):

[0397] Compound (s-4-3) can be prepared in a general nucleophilic substitution reaction or aromatic nucleophilic substitution reaction with compound (s-4-2), Ring G accompanied with a leaving group, and a base. The base used herein includes, for example, an organic base such as triethylamine, diisopropylethylamine, and DBU; an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate; a metal alkoxide such as potassium tert-butoxide; an organometallic reagent such as n-butyl lithium and isopropylmagnesium chloride; and a metal amide reagent such as LDA and LHMDS. The solvent used herein includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (4-3):

[0398] Compound (s-4-1) can be prepared in a similar manner to Step (2-2) with compound (s-4-3).

[0399] Compound (s-4-1) can be also prepared from compound (s-2-5) via Step (4-4)-Step (4-6).

Step (4-4):

[0400] Compound (s-4-4) can be prepared by reacting compound (s-2-5) in a similar manner to Step (2-3) with YH.sub.2 or a reagent equal to YH.sub.2 that includes a protected reagent P.sup.2YH which is deprotected after the addition reaction.

Step (4-5):

[0401] Compound (s-4-5) can be prepared in a similar manner to Step (4-2) with compound (s-4-4).

Step (4-6):

[0402] Compound (s-4-1) can be prepared in a similar deprotection to Step (2-4) with compound (s-4-5).

Preparation Process 5:

[0403] The compound of formula (s-2-5) can be also prepared, for example, by the following process.

##STR00115##

wherein R.sup.3, R.sup.4, and n are as defined in Item 1.

[0404] Compound (s-2-5) can be prepared from compound (s-5-1) via Step (5-1)-Step (5-4).

Step (5-1):

[0405] Compound (s-2-7) can be prepared by reacting compound (s-5-1) in a suitable inert solvent under a conventional condition of epoxide-formulation. The present reaction condition includes, for example, using an oxidizing agent such as hydrogen peroxide solution, mCPBA, tert-butyl hydroperoxide, and Oxone. In the present reaction, a metal catalyst such as V, Mo, Al, Ti, Fe, Ta, Zr, Nb, W, and Re may be used, as appropriate. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (5-2):

[0406] Compound (s-5-2) can be prepared in a similar manner to Step (2-5) with compound (s-2-7) and P.sup.1NH.sub.2 in a suitable inert solvent.

[0407] Step (5-2) may be carried out in a process comprising reacting compound (s-2-7) and ammonia or a reagent equal to ammonia that includes a protected-amine reagent which is deprotected after the amination and an azide-inducer which is reduced after the azidation, and then protecting the product with a protecting group P.sup.1.

Step (5-3):

[0408] Compound (s-5-3) can be prepared in a similar manner to Step (2-6) with compound (s-5-2) in a suitable inert solvent.

Step (5-4):

[0409] Compound (s-2-5) can be prepared by reacting compound (s-5-3) in the presence of a base in a suitable inert solvent under a conventional condition of intramolecular cyclization reaction. The base used herein includes, for example, an organic base such as triethylamine, diisopropylethylamine, and DBU; an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate; a metal alkoxide such as potassium tert-butoxide; an organometallic reagent such as n-butyl lithium and isopropylmagnesium chloride; and a metal amide reagent such as LDA and LHMDS. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

[0410] Step (5-3) and Step (5-4) may be carried out as one step without isolating the intermediate. And, (5-3) and Step (5-4) may be also carried out as one step under Mitsunobu reaction condition.

[0411] Compound (s-2-5) can be also prepared from compound (s-5-1) via Step (5-5).

Step (5-5):

[0412] Compound (s-2-5) can be prepared by reacting compound (s-5-1) in a suitable inert solvent under a conventional condition of aziridine-ring-formulation reaction. The present reaction condition includes, for example, using P.sup.1NH.sub.2 and an oxidizing agent such as iodosylbenzene in the presence of a metallic catalyst, and using a hydroxylamine derivative P.sup.1N(H)O-LG and a metallica catalyst.

Preparation Process 6:

[0413] In compounds according to formula (s-1-1), the compound of formula (s-6-1) which has an unsaturated bond in the ring can be prepared, for example, by the following process.

##STR00116##

wherein R.sup.3, R.sup.4, L.sup.2, n, and Ring G are as defined in Item 1; Z is boronic acid, boronate ester, BF.sub.3K, BF.sub.3Na, trialkyl tin, zinc halide, or hydrogen atom; and X is halogen.

[0414] Compound (s-6-1) can be prepared from compound (s-6-6) via Step (6-7). And, compound (s-6-6) can be prepared from compound (s-6-2) via Step (6-1)-Step (6-3), or via Step (6-4)-Step (6-6).

Step (6-1):

[0415] Compound (s-6-4) wherein L.sup.2 is single bond or methylene which may be optionally substituted with the same or different one or more C.sub.1-4 alkyl can be prepared by reacting compound (s-6-2) with compound (s-6-3) wherein Z is boronic acid, boronate ester, BF.sub.3K, BF.sub.3Na, trialkyl tin, or zinc halide, in the presence of palladium catalyst and phosphine ligand, and optionally in the presence of a base, in a suitable inert solvent. Compound (s-6-3) is commercially available, or can be prepared according to a known method or a similar method thereto. The palladium catalyst used herein includes, for example, tetrakis(triphenylphosphine)palladium(0), bis(dibenzylideneacetone)palladium(0), tris(dibenzylideneacetone)dipalladium(0), bis(tri-tort-butylphosphine)palladium(0), palladium(0) acetate, [1,1-bis(diphenylphosphino) ferrocene]palladium(II) dichloride, and bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II).

[0416] The phosphine ligand used herein includes, for example, dimethoxybiphenyl (S-Phos), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (X-Phos), 1,1′-bis(diphenylphosphino)ferrocene (DPPF), 1,2-bis(diphenylphosphino)ethane (DPPE), 1,3-bis(diphenylphosphino)propane (DPPP), 1,4-bis(diphenylphosphino)butane (DPPB), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (XANT-Phos), and bis((2-diphenylphosphino)phenyl) ether (DPE-Phos). The base used herein includes, for example, sodium carbonate, potassium carbonate, cesium carbonate, potassium phosphate, sodium hydroxide, and potassium hydroxide. The inert solvent includes, for example, 1,4-dioxane, THF, 1,2-dimethoxyethane, acetonitrile, water, and a mixture thereof. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

[0417] In addition, compound (s-6-4) wherein L.sup.2 is O or NR.sup.10 can be also prepared by reacting compound (s-6-2) with compound (s-6-3) wherein Z is hydrogen atom in the presence of palladium catalyst, phosphine ligand, and a base in a suitable inert solvent.

Step (6-2):

[0418] Compound (s-6-5) can be prepared in a similar manner to Step (2-6) with compound (s-6-4).

Step (6-3):

[0419] Compound (s-6-6) can be prepared in a similar manner to Step (2-7) with compound (s-6-5) and P.sup.1NH.sub.2.

[0420] Step (6-3) may be carried out in a process comprising reacting compound (s-6-5) and ammonia or a reagent equal to ammonia that includes a protected-amine reagent which is deprotected after the amination and an azide-inducer which is reduced after the azidation, and then protecting the product with a protecting group P.sup.1.

[0421] Step (6-2) and Step (6-3) may be carried out as one step without isolating the intermediate. And, Step (6-2) and Step (6-3) may be also carried out as one step under Mitsunobu reaction condition.

Step (6-4):

[0422] Compound (s-6-7) can be prepared in a similar manner to Step (6-2) with compound (s-6-2).

Step (6-5):

[0423] Compound (s-6-8) can be prepared in a similar manner to Step (6-3) with compound (s-6-7).

[0424] Step (6-5) may be carried out in a process comprising reacting compound (s-6-7) and ammonia or a reagent equal to ammonia that includes a protected-amine reagent which is deprotected after the amination and an azide-inducer which is reduced after the azidation, and then protecting the product with a protecting group P.sup.1.

[0425] Step (6-4) and Step (6-5) may be carried out as one step without isolating the intermediate. And, Step (6-4) and Step (6-5) may be also carried out as one step under Mitsunobu reaction condition.

Step (6-6):

[0426] Compound (s-6-6) can be prepared in a similar manner to Step (6-1) with compound (s-6-8).

Step (6-7):

[0427] Compound (s-6-1) can be prepared in a similar deprotection to Step (2-4) with compound (s-6-6).

[0428] Preparation Process 7:

[0429] In compounds according to formula (s-1-1), the compound of formula (s-7-1) which has no unsaturated bond in the ring can be prepared, for example, by the following process.

##STR00117##

wherein R.sup.1-R.sup.4, L.sup.1, L.sup.2, n, Ring G, and A.sup.1 are as defined in Item 1.

[0430] Compound (s-7-1) can be prepared from compound (s-7-4) via Step (7-6). And, compound (s-7-4) can be prepared from compound (s-5-3) via Step (7-1) Step (7-3), or from compound (s-2-5) via Step (7-4) and Step (7-5).

Step (7-1):

[0431] Compound (s-7-2) can be prepared in a similar deprotection to Step (2-4) with compound (s-5-3).

Step (7-2):

[0432] Compound (s-7-3) can be prepared in a similar ureation to Step (1-1) with compound (s-7-2) and compound (s-1-2). In this step, the hydroxy group may be protected and deprotected, if necessary.

Step (7-3):

[0433] Compound (s-7-4) can be prepared in a similar manner to Step (5-3) and Step (5-4) with compound (s-7-3).

Step (7-4):

[0434] Compound (s-7-5) can be prepared in a similar deprotection to Step (2-4) with compound (s-2-5).

Step (7-5):

[0435] Compound (s-7-4) can be prepared in a similar urea formation to Step (1-1) with compound (s-7-5) and compound (s-1-2).

Step (7-6):

[0436] Compound (s-7-1) can be prepared in a similar aziridine-ring-open reaction to Step (2-3) with compound (s-7-4) and compound (s-2-3).

Preparation Process 8:

[0437] The compound of formula (s-1-1) can be also prepared from compound (s-8-1) via Step (8-1)-Step (8-3).

##STR00118##

wherein R.sup.1-R.sup.4, L.sup.1, L.sup.2, n, Ring G, A.sup.1, and the bond accompanied with broken line are as defined in Item 1.

Step (8-1):

[0438] Compound (s-8-2) can be prepared by reacting compound (s-8-1) in a suitable inert solvent under a conventional condition of acyl azide formulation. The present reaction condition includes, for example, using diphenylphosphoryl azide, or converting the carboxylic acid to its acid halide and then azidating the acid halide with a metallic azide. The inert solvent includes an ether solvent such as diethyl ether, diisopropyl ether, tetrahydrofuran, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene, an ester solvent such as ethyl acetate and methyl acetate; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone, 1,3-dimethyl-2-imidazolidinone, and dimethyl sulfoxide. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (8-2):

[0439] Compound (s-8-3) can be prepared by reacting compound (s-8-2) in a suitable inert solvent under a condition of Curtius rearrangement reaction. Compound (s-8-2) used herein may be the un-isolated product from the prior step.

Step (8-3):

[0440] Compound (s-1-1) can be prepared by reacting compound (s-8-3) and compound (s-1-2) in a suitable inert solvent under a conventional condition of addition reaction. Compound (s-8-3) used herein may be the un-isolated product from the prior step.

Preparation Process 9:

[0441] In compounds according to formula (s-8-1), the compound of formula (s-9-1) which has no unsaturated bond in the ring can be prepared, for example, by the following process.

##STR00119##

wherein R.sup.3, R.sup.4, L.sup.2, n, and Ring G are as defined in Item 1; and P.sup.3 is a suitable protecting group or C.sub.1-3 alkyl, said definitions are used below unless otherwise indicated.

[0442] Compound (s-9-1) can be prepared from compound (s-9-2) via Step (9-1) and Step (9-2).

Step (9-1):

[0443] Compound (s-9-3) can be prepared in a similar manner to Step (2-1) with compound (s-9-2) and compound (s-2-3).

Step (9-2):

[0444] Compound (s-9-1) can be prepared by subjecting compound (s-9-3) to a general condition of hydrolysis or deprotection.

[0445] Compound (s-9-1) can be prepared from compound (s-2-9) via Step (9-3) and Step (9-4).

Step (9-3):

[0446] Compound (s-9-4) can be prepared in a similar manner to Step (2-7) with compound (s-2-9) and a metallic cyanide.

Step (9-4):

[0447] Compound (s-9-1) can be prepared by reacting compound (s-9-4) in a suitable inert solvent under a general condition of hydrolysis.

Preparation Process 10:

[0448] In compounds according to formula (s-8-1), the compound of formula (s-10-1) which has an unsaturated bond in the ring can be prepared, for example, by the following process.

##STR00120##

wherein R.sup.3, R.sup.4, L.sup.2, n, and Ring G are as defined in Item 1; Z is boronic acid, boronate ester, BF.sub.3K, BF.sub.3Na, trialkyl tin, zinc halide, or hydrogen atom; and X is halogen.

[0449] Compound (s-10-1) can be prepared from compound (s-10-2) via Step (10-2). And, compound (s-10-2) can be prepared from compound (s-6-5) via Step (10-1), or from compound (s-6-7) via Step (10-3) and Step (10-4).

Step (10-1):

[0450] Compound (s-10-2) can be prepared in a similar manner to Step (2-7) with compound (s-6-5) and a metallic cyanide.

Step (10-2):

[0451] Compound (s-10-1) can be prepared by reacting compound (s-10-2) in a suitable inert solvent under a general condition of hydrolysis.

Step (10-3):

[0452] Compound (s-10-3) can be prepared in a similar manner to Step (10-1) with compound (s-6-7) and a metallic cyanide.

Step (10-4):

[0453] Compound (s-10-2) can be prepared in a similar manner to Step (6-1) with compound (s-10-3) and compound (s-6-3).

Preparation Process 11:

[0454] In compounds according to formula (1) or a pharmaceutically acceptable salt thereof, the compound of formula (s-11-1) which is a compound of formula (1) wherein A.sup.3 is carbon atom or a pharmaceutically acceptable salt thereof can be prepared, for example, by the following process.

##STR00121##

wherein R.sup.1-R.sup.4, L.sup.1, L.sup.2, n, Ring G, and the bond accompanied with broken line are as defined in Item 1.

Step (11-1):

[0455] Compound (s-11-1) can be prepared by reacting compound (s-11-2) and compound (s-1-3) in a suitable inert solvent under a conventional condition of amide-bond formulation reaction. The present reaction condition includes, for example, using a condensation agent and a base, and the condensation agent used herein includes, for example, a carbodiimide such as dicyclohexylcarbodiimide, 1,1′-carbonyldiimidazole, diphenylphosphoryl azide (DPPA), diethylphosphoryl cyanide (DEPC), dicyclohexylcarbodiimide (DCC), carbonyldiimidazole (CDI), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDO.HCl), O-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl-uronium tetrahydroborate (TBTU), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HBTU), and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′,-tetramethyluronium hexafluorophosphate (HATU). The base used herein includes an organic base such as triethylamine, diisopropylethylamine, tributylamine, DBU, pyridine, and dimethylaminopyridine. The inert solvent includes a halogenated hydrocarbon solvent such as dichloromethane and chloroform; an ether solvent such as diethyl ether, diisopropyl ether, tetrahydrofuran, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; an ester solvent such as ethyl acetate and methyl acetate; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone, 1,3-dimethyl-2-imidazolidinone, and dimethyl sulfoxide. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

[0456] Compound (s-11-1) can be also prepared from compound (s-11-2) via Step (11-2) and Step (11-3).

Step (11-2):

[0457] Compound (s-11-3) can be prepared by reacting compound (s-11-2) in a suitable inert solvent under a conventional condition of acid halide formulation reaction. The present reaction condition includes, for example, using a halogenating agent, and the halogenating agent used herein includes, for example, thionyl chloride, oxalyl chloride, phosphoryl chloride, sulfuryl chloride, phosphorus trichloride, phosphorus tribromide, and phosphorus pentachloride. The inert solvent includes a halogenated hydrocarbon solvent such as dichloromethane and chloroform; an ether solvent such as diethyl ether, diisopropyl ether, tetrahydrofuran, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (11-3):

[0458] Compound (s-11-1) can be prepared by reacting compound (s-11-3) and compound (s-1-3) in a suitable inert solvent in the presence of a base. The base used herein includes an organic base such as triethylamine, diisopropylethylamine, tributylamine, DBU, pyridine, and dimethylaminopyridine; and an inorganic base such as sodium hydrogen carbonate, sodium carbonate, and potassium carbonate. The inert solvent includes a halogenated hydrocarbon solvent such as dichloromethane and chloroform; an ether solvent such as diethyl ether, diisopropyl ether, tetrahydrofuran, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Preparation Process 12:

[0459] In compounds according to formula (1) or a pharmaceutically acceptable salt thereof, the compound of formula (s-12-1) which is a compound of formula (1) wherein A.sup.2 is oxygen atom or a pharmaceutically acceptable salt thereof can be prepared, for example, by the following process.

##STR00122##

wherein R.sup.1-R.sup.4, L.sup.1, L.sup.2, n, Ring G, A.sup.1, and the bond accompanied with broken line are as defined in Item 1.

Step (12-1):

[0460] Compound (s-12-1) can be prepared by reacting compound (s-1-2) and compound (s-12-2) in a suitable inert solvent under a conventional condition of carbamate formulation reaction. The present reaction condition includes, for example, using triphosgene, 4-nitrophenyl chloroformate, or thiophosgene. A base is used in the present reaction, and the base used herein includes triethylamine and diisopropylethylamine. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

[0461] Compound (s-12-2) which has no unsaturated bond in the ring is prepared in the Preparation Process of compound (s-2-8). And, compound (s-12-2) which has a unsaturated bond in the ring is prepared in the Preparation Process of compound (s-6-4).

Preparation Process 13:

[0462] In compounds according to formula (s-1-2), the compound of formula (s-13-1) can be prepared, for example, by the following process.

##STR00123##

wherein R.sup.2 is as defined in Item 1, R.sup.a1 and Q.sup.2 are as defined in Item 4; and P.sup.4 is a suitable protecting group, said definitions are used below unless otherwise indicated.

Step (13-1):

[0463] Compound (s-13-4) can be prepared by reacting compound (s-13-2) and compound (s-13-3) in a suitable inert solvent under a conventional condition of addition reaction. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; an alcohol solvent such as methanol and ethanol; and water. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (13-2):

[0464] Compound (s-13-6) can be prepared by reacting compound (s-13-4) and compound (s-13-5) in a suitable inert solvent under a conventional condition of condensation reaction. The present reaction condition includes, for example, using HATU, DCC, or CDI. A base is used in the present reaction, and the base used herein includes triethylamine and diisopropylethylamine. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (13-3):

[0465] Compound (s-13-7) can be prepared by reacting compound (s-13-6) in a suitable inert solvent under a conventional condition of dehydration reaction. In the present reaction, a base such as triethylamine and DBU may be used as appropriate. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (13-4):

[0466] Compound (s-13-1) can be prepared by deprotecting compound (s-13-7) in a known manner (for example, a manner described in Protective Groups in Organic Synthesis 3.sup.rd Edition (John Wiley & Sons, Inc.), Comprehensive Organic Transformation, edited by R. C. Larock, VCH publisher Inc., 1989, etc.) or a similar manner thereto.

Preparation Process 14:

[0467] In compounds according to formula (s-1-2), the compound of formula (s-14-1) which is a compound of formula (s-1-2) wherein L.sup.1 is single bond and R.sup.1 is optionally-substituted 5-membered aromatic heterocyclyl group can be also prepared, for example, by the following process.

##STR00124##

wherein R.sup.2 is as defined in Item 1, X.sup.4 and R.sup.a1 are as defined in Item 4.

[0468] Compound (s-14-1) can be prepared from compound (s-14-2) via Step (14-1)-Step (14-3).

Step (14-1):

[0469] Compound (s-14-3) can be prepared by reacting compound (s-14-2) in a suitable inert solvent under a conventional condition of chlorination reaction. The present reaction condition includes, for example, using chlorine, N-succinimide, and trimethylbenzylammonium tetrachloroiodate. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone, 1,3-dimethyl-2-imidazolidinone and dimethyl sulfoxide; water; and a mixture thereof. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (14-2):

[0470] Compound (s-14-5) can be prepared by reacting compound (s-14-3) and compound (s-14-4) in a suitable inert solvent under a conventional condition of 1,3-dipolar cycloaddition reaction. The present reaction condition includes, for example, using a base, and the base used herein includes an inorganic base such as potassium carbonate, cesium carbonate, sodium carbonate, sodium hydrogen carbonate, sodium methoxide, sodium t-butoxide, sodium hydroxide, potassium hydroxide, and potassium fluoride; and an organic base such as triethylamine, diisopropylethylamine, tributylamine, DBN, DABCO, DBU, pyridine, dimethylaminopyridine, picoline, and NMM. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (14-3):

[0471] Compound (s-14-1) can be prepared in a similar manner to Step (13-4) with compound (s-14-5).

Preparation Process 15:

[0472] In compounds according to formula (s-1-2), the compound of formula (s-15-1) can be prepared, for example, by the following process.

##STR00125##

wherein R.sup.2 is as defined in Item 1, X.sup.1-X.sup.3, Q.sup.1 and R.sup.a6 are as defined in Item 4.

Step (15-1):

[0473] Compound (s-15-4) can be prepared by reacting compound (s-15-2) and compound (s-15-3) in a suitable inert solvent under a condensation reaction like Step (13-2).

Step (15-2):

[0474] Compound (s-15-5) can be prepared by reacting compound (s-15-4) in a suitable inert solvent under a conventional condition of dehydration reaction, or a cyclization condition after the treatment with Lawesson's reagent or the like.

Step (15-3):

[0475] Compound (s-15-1) can be prepared in a similar manner to Step (13-4) with compound (s-15-5).

Preparation Process 16:

[0476] In compounds according to formula (s-1-2), the compound of formula (s-16-5) or the compound of formula (s-16-8) which is a compound of formula (s-1-2) wherein L.sup.1 is single bond and R.sup.1 is optionally-substituted C.sub.6-10 aromatic carbocyclyl group or optionally-substituted 5- to 10-membered aromatic heterocyclyl group can be prepared, for example, by the following process.

##STR00126##

wherein R.sup.1 and R.sup.2 are as defined in Item 1; Z is exemplified in the following Step (16-1); and X is halogen.

[0477] Compound (s-16-5) can be prepared from compound (s-16-1) via Step (16-1)-Step (16-3).

Step (16-1):

[0478] Compound (s-16-3) can be prepared by coupling compound (s-16-1) with organic boron compound (for example, Z is B(OH).sub.2 and the like), organic zinc compound (for example, Z is ZnCl and the like), alkenyl compound, alkynyl compound, hydroxy compound (for example, Z is OH and the like), amine compound (for example, Z is NH.sub.2 and the like), or metallic cyanide (for example, Z is CuCN and the like), in the presence of a base and metallic catalyst. The base used herein includes an inorganic base such as potassium carbonate, cesium carbonate, sodium carbonate, sodium hydrogen carbonate, sodium methoxide, sodium t-butoxide, sodium hydroxide, potassium hydroxide, and potassium fluoride; and an organic base such as triethylamine, diisopropylethylamine, tributylamine, DBN, DABCO, DBU, pyridine, dimethylaminopyridine, picoline, and NMM. Sometimes, a base is not used depending on the coupling type. The metallic catalyst used herein includes, for example, bis(tri-tert-butylphosphine)palladium, bis(tri-o-tolylphosphine)dichloropalladium, bis(tri-o-tolylphosphine)palladium, tetrakis(triphenylphosphine)palladium, dichlorobis(acetonitrile)palladium, bis(tri-o-tolylphosphine)dichloropalladium, [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium, and PEPPSI™.IPr((1,3-bis(2,6-diisopropylphenyl)imidazolidene) (3-chloropyridyl)palladium(II)dichloride). Palladium acetate or palladium chloride may be used herein, and a ligand described in Palladium reagents and catalysts, John Wiley & Sons Inc. (2004) or a similar ligand may be also used in place of the acetate in palladium acetate or the chloride in palladium chloride. The solvent used herein includes, for example, an ether solvent such as diethyl ether, diisopropyl ether, tetrahydrofuran, methyl cyclopentyl ether, anisole, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, chlorobenzene, and xylene; an ester solvent such as ethyl acetate and methyl acetate; an aprotic polar solvent such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone, 1,3-dimethyl-2-imidazolidinone, and dimethyl sulfoxide; water; and a mixture thereof. The reaction temperature should be determined depending on the starting compound to be used, which is generally about 0° C. to about 250° C., preferably about 20° C. to about 200° C. The reaction time is generally 30 minutes to 48 hours, preferably 1 to 24 hours.

Step (16-2):

[0479] Compound (s-16-4) can be prepared by reacting compound (s-16-3) in a suitable inert solvent under a conventional condition of alkene-reduction reaction, and under hydrogen atmosphere if necessary. The present reaction condition includes, for example, using a reducing agent such as palladium carbon, palladium(II) hydroxide, platinum on carbon, platinum(IV) oxide, Raney nickel, ruthenium carbon, and tris(triphenylphosphine)rhodium(I) chloride. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; an aromatic hydrocarbon solvent such as benzene, toluene, and xylene; an alcohol solvent such as methanol and ethanol; and an ester solvent such as ethyl acetate and methyl acetate. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (16-3):

[0480] Compound (s-16-5) can be prepared in a similar manner to Step (13-4) with compound (s-16-4).

[0481] Compound (s-16-8) can be prepared from compound (s-16-1) via Step (16-1), and Step (16-4)-Step (16-6).

Step (16-4):

[0482] Compound (s-16-6) can be prepared by reacting compound (s-16-3), an alkylating agent R.sup.2—X, and a base in a suitable inert solvent under a condition of alkylation reaction. The base used herein includes LDA, LHMDS, and n-butyllithium. The inert solvent includes a ether solvent such as diethyl ether, THF, and 1,4-dioxane; and an aromatic hydrocarbon solvent such as benzene, toluene, and xylene. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (16-5):

[0483] Compound (s-16-7) can be prepared by reacting compound (s-16-6) in a suitable inert solvent in a similar manner to Step (16-2) wherein the reducing agent may include sodium borohydride, sodium cyanoborohydride, and sodium triacetoxyborohydride.

Step (16-6):

[0484] Compound (s-16-8) can be prepared in a similar manner to Step (13-4) with compound (s-16-7).

Preparation Process 17:

[0485] In compounds according to formula (s-1-2), the compound of formula (s-17-1) can be prepared, for example, by the following process.

##STR00127##

wherein R.sup.1 is as defined in Item 1, and R.sup.8 is C.sub.1-3 alkyl.

Step (17-1):

[0486] Compound (s-17-3) can be prepared by reacting compound (s-17-2) and an alkylating agent R.sup.1—X wherein X is halogen in a suitable inert solvent under a condition of alkylation reaction like Step (16-4).

Step (17-2):

[0487] Compound (s-17-4) can be prepared by reacting compound (s-17-3) in a suitable inert solvent under a conventional condition of reduction reaction. The present reaction condition includes, for example, using LAH or DIBAL. The inert solvent includes a halogenated carbon solvent such as chloroform and dichloromethane; a ether solvent such as diethyl ether, THF, and 1,4-dioxane; and an aromatic hydrocarbon solvent such as benzene, toluene, and xylene. The reaction time is generally about 1 hour to 24 hours, and the reaction temperature is −20° C. to boiling point of a solvent used herein.

Step (17-3):

[0488] Compound (s-17-5) can be prepared by reacting compound (s-17-4) in a suitable inert solvent under a condition of Barton-McCombie deoxygenation.

Step (17-4):

[0489] Compound (s-17-1) can be prepared in a similar manner to Step (13-4) with compound (s-17-5).

EXAMPLES

[0490] The present invention is explained in more detail in the following by referring to Reference examples, Examples, and Tests; however, the technical scope of the present invention should not be limited thereto. It should be understood that the names of compounds used in the following Reference examples and Examples do not necessarily follow the IUPAC nomenclature.

[0491] In the present specification, the abbreviations shown below may be used.

CDCl.sub.3: deuterochloroform
DMSO-d.sub.6: deuterodimethylsulfoxide
Rt: retention time
min: minute
HATU: O-(7-aza-1H-benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate
DCC: N,N′-dicyclohexylcarbodiimide
CDI: carbonyldiimidazole
THF: tetrahydrofuran
TFA: trifluoroacetic acid

DMF: N,N-dimethylformamide

[0492] DMSO: dimethyl sulfoxide
CPME: cyclopentyl methyl ether
Boc: tert-butoxycarbonyl
Ns: 2-nitrobenzenesulfonyl
Tf: trifluoromethanesulfonyl
DBU: diazabicycloundecene
DBN: 1,5-diazabicyclo[4.3.0]non-5-ene
LDA: lithium diisopropylamide
LHMDS: lithium bis(trimethylsilyl)amide
mCPBA: meLa-chloroperbenzoic acid
DABCO: 1,4-diazabicyclo[2.2.2]octane

NMM: N-methylmorpholine

[0493] LAH: lithium aluminium hydride
DIBAL: diisobutylaluminium hydride
Abs: Absolute Configuration; each chemical structure of compounds described along with Abs mark surrounded with a square flame is shown in absolute configuration with a wedged bond. However, not all compounds without Abs mark are shown in non-absolute configuration, i.e., the configuration should be properly judged based on the disclosure about the subject compound in the present description and its context, and a skilled person's technical knowledge, with or without Abs mark.

[0494] In the column chromatography and amino chromatography used in Reference examples and Examples, silica gel column and amino column made by YAMAZEN CORPORATION were used. The TLC (silica gel plate) used in the TLC purification was Silica gel 60F254 (Merck), and the TLC (NH silica gel plate) used therein was TLC plate NH (FujiSilysia).

[0495] In Reference examples and Examples, the reactors shown below were used. The physicochemical data described in Reference examples and Examples were obtained with the apparatuses below.

Microwave reactor: Biotage AB Initiator

[0496] .sup.1H-NMR: JEOL JNM-AL400; JEOL JNM-ECS400; Brucker AVANCE 400 Spectrometer

[0497] The symbols used in NMR are defined as follows, s: singlet, d: doublet, dd: doublet of doublet, ddd: doublet of doublet of doublet, dddd: doublet of doublet of doublet of doublet, t: triplet, td: triplet of doublet, q: quartet, m: multiplet, br: broad singlet or multiplet, and J: coupling constant.

[0498] The LC/MS data of each compound in Examples and Reference examples were obtained with any one of the apparatuses below.

Method A

[0499] Detection apparatus: ACQUITY™ SQ detector (Waters Corporation)

HPLC: ACQUITY™ UPLC SYSTEM

[0500] Column: Waters ACQUITY™ UPLC BEH C18 (1.7 μm, 2.1 mm×30 mm)

Method B

[0501] Detection apparatus: Shimadzu LCMS-2020
Column: Phenomenex Kinetex (C18, 1.7 μm, 2.1 mm×50 mm)

Method C

[0502] Detection apparatus: ACQUITY™ SQ detector (Waters Corporation)

HPLC: ACQUITY™ UPLC SYSTEM

[0503] Column: Waters ACQUITY™ UPLC BEH C18 (1.7 μm, 2.1 mm×30 mm)

[0504] High-performance liquid chromatograph mass spectrometer; the measurement conditions of LC/MS are as follows, wherein the observed [MS (m/z)] is denoted by [M+H].sup.+ and the retention time is denoted by Rt (min). Each measured MS value shown in the working examples is accompanied by any one of A-D which were measurement methods used in the actual measurements.

Method A

[0505] Solvent: A; 0.06% formic acid/H.sub.2O, B; 0.06% formic acid/acetonitrile
Gradient condition: 0.0-1.3 min (linear gradient from B 2% to B 96%)
Flow rate: 0.8 mL/min; Detective UV: 220 nm and 254 nm; Temperature: 40° C.

[0506] Hereinafter, the LC-MS data shown below were measured by Method A, unless otherwise indicated.

Method B

[0507] Solvent: A; 0.05% TFA/H.sub.2O, B; acetonitrile
Gradient condition: 0.0-1.7 min (linear gradient from B 10% to B 99%)
Flow rate: 0.5 mL/min; Detective UV: 220 nm; Temperature: 40° C.

Method C

[0508] Solvent: A; 0.05% formic acid/H.sub.2O, B; acetonitrile
Gradient condition: 0.0-1.3 min (linear gradient from B 10% to B 95%) 1.3-1.5 min (B 10%)
Flow rate: 0.8 mL/min; Detective UV: 220 nm and 254 nm; Temperature: 40° C.

Example 1

rac-4-(4-Methylphenyl)-N-{(1S,2S)-2-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}piperidine-1-carboxamide

[0509] ##STR00128##

[0510] To a mixture of Reference example 1 (211 mg) (Material A), triethylamine (0.391 mL), and chloroform (3 mL) was added 4-nitrophenyl chloroformate (208 mg) at 0° C., and the mixture was stirred at the same temperature for 40 minutes. To the reaction mixture was added 4-(4-methylphenyl)piperidine hydrochloride (238 mg) (Material B) at 0° C., and the mixture was stirred at room temperature for one hour. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound (346 mg).

[0511] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (6H, d, J=6.7 Hz), 1.04-1.11 (1H, m), 1.12-1.40 (3H, m), 1.58-1.71 (3H, m), 1.76-1.93 (4H, m), 2.27 (1H, dd, J=10.4, 3.6 Hz), 2.32 (3H, s), 2.35-2.54 (6H, m), 2.54-2.65 (3H, m), 2.65-2.75 (2H, m), 2.78-2.91 (2H, m), 3.25-3.33 (1H, m), 4.08-4.19 (2H, m), 5.76 (1H, s), 7.09 (2H, d, J=8.8 Hz), 7.12 (2H, d, J=8.8 Hz).

Examples 2 to 16

[0512] The compounds of Examples 2 to 16 shown in the table below were prepared in the same manner as Example 1, by using commercial compounds or Reference example compounds which correspond to Material A and Material B described in Example 1.

TABLE-US-00001 Structure Material A Material B Example Spectral data Reference Commercial 2 example 3 product [00129] [00130] [00131] .sup.1H-NMR (CDCl.sub.3) δ: 1.07 (3H, t, J = 7.3 Hz), 1.12-1.35 (6H, m), 1.36-1.45 (2H, m), 1.56-1.69 (2H, m), 1.80- 1.88 (2H, m), 1.89-1.96 (1H, m), 2.12-2.20 (1H, m), 2.30-2.58 (11H, m), 2.59-2.70 (2H, m), 2.80-2.91 (2H, m), 3.98-4.04 (1H, m), 4.07-4.15 (2H, m), 5.16 (1H, s), 7.10 (2H, d, J = 8.5 Hz), 7.13 (2H, d, J = 8.5 Hz). Reference Commercial 3 example 1 product [00132] [00133] [00134] .sup.1H-NMR (CDCl.sub.3) δ: 1.03 (6H, d, J = 6.1 Hz), 1.14-1.28 (3H, m), 1.32 (3H, s), 1.58-1.68 (3H, m), 1.76-1.82 (1H, m), 1.83-1.91 (1H, m), 2.19-2.30 (3H, m), 2.34- 2.53 (6H, m), 2.53-2.62 (6H, m), 2.62-2.71 (2H, m), 3.07 (2H, ddd, J = 13.2, 10.4, 2.8 Hz), 3.20-3.31 (1H, m), 3.63-3.74 (2H, m), 5.70 (1H, s). Reference Commercial 4 example 4 product [00135] [00136] [00137] .sup.1H-NMR (CDCl.sub.3) δ: 1.01 (6H, d, J = 6.1 Hz), 1.15-1.35 (4H, m), 1.42-1.58 (2H, m), 1.58-1.71 (2H, m), 1.81- 1.90 (2H, m), 1.91-2.01 (1H, m), 2.32 (3H, s), 2.38- 2.63 (8H, m), 2.63-2.71 (3H, m), 2.72-2.95 (3H, m), 3.35 (3H, s), 3.50-3.57 (1H, m), 4.01-4.06 (1H, m), 4.06-4.23 (2H, m), 5.53 (1H, d, J = 3.7 Hz), 7.09 (2H, d, J = 8.2 Hz), 7.12 (2H, d, J = 8.2 Hz). Reference Commercial 5 example 5 product [00138] [00139] [00140] .sup.1H-NMR (CDCl.sub.3) δ: 1.06 (6H, d, J = 6.1 Hz), 1.35-1.48 (1H, m), 1.48-1.73 (5H, m), 1.78-1.91 (2H, m), 2.12- 2.25 (1H, m), 2.32 (3H, s), 2.39-2.79 (12H, m), 2.79- 2.93 (2H, m), 3.96-4.12 (3H, m), 4.63 (1H, s), 7.09 (2H, d, J = 7.9 Hz), 7.12 (2H, d, J = 7.9 Hz). Reference Reference 6 example 5 example 20 [00141] [00142] [00143] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-0.99 (2H, m), 0.99-1.09 (8H, m), 1.26 (3H, s), 1.35-1.45 (1H, m), 1.46-1.76 (6H, m), 1.80-1.90 (1H, m), 1.94-2.10 (3H, m), 2.10-2.21 (1H, m), 2.37-2.84 (9H, m), 3.08-3.17 (2H, m), 3.52- 3.64 (2H, m), 3.98-4.08 (1H, m), 4.61 (1H, s), 5.77 (1H, s). Reference Reference 7 example 7 example 8 [00144] [00145] [00146] .sup.1H-NMR (CDCl.sub.3) δ: 0.80-0.91 (1H, m), 1.02 (3H, d, J = 6.0 Hz), 1.03 (3H, d, J = 6.0 Hz), 1.18-1.23 (4H, m), 1.24-1.28 (2H, m), 1.31 (3H, s), 1.53-1.70 (2H, m), 1.92-2.28 (5H, m), 2.28-2.69 (7H, m), 2.73-2.81 (2H, m), 3.02-3.14 (4H, m), 3.52-3.63 (1H, m), 3.63-3.75 (2H, m), 5.52 (1H, s). Reference Commercial 8 example 14 product [00147] [00148] [00149] .sup.1H-NMR (CDCl.sub.3) δ: 0.96-1.52 (11H, m), 1.70-1.93 (3H, m), 1.94-2.08 (2H, m), 2.13-2.26 (1H, m), 2.32 (3H, s), 2.42-3.27 (12H, m), 4.02-4.26 (3H, m), 4.61 (1H, d, J = 6.7 Hz), 7.08 (2H, d, J = 8.5 Hz), 7.12 (2H, d, J = 8.5 Hz). Reference Reference 9 example 6 example 8 [00150] [00151] [00152] .sup.1H-NMR (CDCl.sub.3) δ: 1.46-1.63 (6H, m), 1.12-1.24 (4H, m), 1.24-1.39 (5H, m), 1.39-1.50 (1H, m), 1.51-1.71 (3H, m), 1.86-1.96 (1H, m), 2.07-2.29 (4H, m), 2.31- 2.59 (6H, m), 2.59-2.74 (2H, m), 2.74-2.89 (2H, m), 2.93-3.17 (1H, m), 3.18-3.41 (1H, m), 3.62-3.83 (1H, m), 3.83-4.00 (1H, m), 4.82-5.00 (1H, m). Reference Commercial 10 example 6 product [00153] [00154] [00155] .sup.1H-NMR (CDCl.sub.3) δ: 0.88-1.10 (6H, m), 1.23-1.39 (1H, m), 1.33 (3H, s), 1.40-1.51 (1H, m), 1.53-2.99 (2H, m), 1.73-1.83 (1H, m), 1.83-1.96 (1H, m), 2.06-2.31 (3H, m), 2.31-2.60 (9H, m), 2.60-2.86 (3H, m), 2.90- 3.16 (1H, m), 3.16-3.42 (1H, m), 3.63-3.86 (1H, m), 3.86-4.03 (1H, m), 4.83-5.00 (1H, m). Reference Reference 11 example 6 example 20 [00156] [00157] [00158] .sup.1H-NMR (CDCl.sub.3) δ: 0.90-1.10 (10H, m), 1.15-1.37 (5H, m), 1.37-1.50 (1H, m), 1.53-1.81 (4H, m), 1.83-1.95 (1H, m), 1.95-2.24 (4H, m), 2.24-2.71 (7H, m), 2.71- 2.87 (2H, m), 3.01-3.49 (2H, m), 3.60-3.81 (1H, m), 3.81-3.97 (1H, m), 4.83-5.00 (1H, m), 5.77 (1H, s). Reference Reference 12 example 6 example 10 [00159] [00160] [00161] .sup.1H-NMR (CDCl.sub.3) δ: 0.82-1.12 (6H, m), 1.23-1.50 (5H, m), 1.56-1.83 (4H, m), 1.85-1.97 (1H, m), 2.10-2.33 (3H, m), 2.33-2.73 (8H, m), 2.73-2.88 (2H, m), 2.95- 3.22 (1H, m), 3.21-3.48 (1H, m), 3.65-3.84 (1H, m), 3.86-4.04 (1H, m), 4.85-5.00 (1H, m), 6.79 (1H, t, J = 52.3 Hz). Reference Reference 13 example 6 example 27 [00162] [00163] [00164] .sup.1H-NMR (CDCl.sub.3) δ: 0.83-1.15 (10H, m), 1.18-1.34 (1H, m), 1.29 (3H, s), 1.34-1.50 (1H, m), 1.52-1.72 (3H, m), 1.72-1.82 (1H, m), 1.83-1.97 (1H, m), 2.08-2.21 (1H, m), 2.21-2.60 (8H, m), 2.60-2.73 (2H, m), 2.73- 2.89 (2H, m), 2.91-3.11 (1H, m), 3.14-3.37 (1H, m), 3.42-3.59 (1H, m), 3.59-3.83 (1H, m), 3.83-4.03 (1H, m), 4.79-5.02 (1H, m), 8.00 (1H, s). Reference Reference 14 example 42 example 8 [00165] [00166] [00167] .sup.1H-NMR (CDCl.sub.3) δ: 1.46-1.63 (6H, m), 1.12-1.24 (4H, m), 1.24-1.39 (5H, m), 1.39-1.50 (1H, m), 1.51-1.71 (3H, m), 1.86-1.96 (1H, m), 2.07-2.29 (4H, m), 2.31- 2.59 (6H, m), 2.59-2.74 (2H, m), 2.74-2.89 (2H, m), 2.93-3.17 (1H, m), 3.18-3.41 (1H, m), 3.62-3.83 (1H, m), 3.83-4.00 (1H, m), 4.82-5.00 (1H, m). Reference Reference 15 example 44 example 20 [00168] [00169] [00170] .sup.1H-NMR (CDCl.sub.3) δ: 0.89-0.98 (2H, m), 0.98-1.06 (2H, m), 1.18 (3H, s), 1.28 (6H, d, J = 7.3 Hz), 1.32-1.41 (1H, m), 1.41-1.54 (1H, m), 1.54-1.79 (2H, m), 1.79- 2.05 (5H, m), 2.12-2.32 (2H, m), 2.91-3.09 (3H, m), 3.35-3.44 (1H, m), 3.50-3.59 (1H, m), 4.37 (1H, d, J = 7.9 Hz), 4.90-4.97 (1H, m), 5.72 (1H, s), 6.26 (1H, dd, J = 3.7, 3.7 Hz), 7.10 (1H, d, J = 8.3 Hz), 7.61 (1H, dd, J = 8.3, 2.0 Hz), 8.55 (1H, d, J = 2.0 Hz). Reference Reference 16 example 44 example 8 [00171] [00172] [00173] .sup.1H-NMR (CDCl.sub.3) δ: 1.15-1.20 (4H, m), 1.23 (3H, s), 1.24-1.32 (1H, m), 1.28 (6H, d, J = 6.7 Hz), 1.37 (1H, ddd, J = 14.1, 10.3, 3.6 Hz), 1.50 (1H, ddd, J = 14.1, 10.3, 3.8 Hz), 1.69-1.79 (1H, m), 1.79-1.97 (2H, m), 2.02-2.18 (3H, m), 2.18-2.34 (2H, m), 2.84- 3.09 (3H, m), 3.39-3.48 (1H, m), 3.53-3.61 (1H, m), 4.36 (1H, d, J = 7.9 Hz), 4.91-4.98 (1H, m), 6.27 (1H, dd, J = 4.0, 4.0 Hz), 7.10 (1H, d, J = 8.2 Hz), 7.61 (1H, dd, J = 8.2, 2.1 Hz), 8.56 (1H, d, J = 2.1 Hz).

[0513] The chemical names of Example 2 to Example 16 are listed below.

Example 2: rac-N-[(1R,2S)-2-(4-ethylpiperazin-1-yl)cyclohexyl]-4-(4-methylphenyl)piperidine-1-carboxamide

Example 3: rac-4-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)-N-{(1S,2S)-2-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}piperidine-1-carboxamide

Example 4: rac-N-{(1R,2S,6S)-2-methoxy-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(4-methylphenyl)piperidine-1-carboxamide

Example 5: rac-4-(4-methylphenyl)-N-{(1S,2S)-2-[4-(propan-2-yl)piperazin-1-yl]cyclopentyl}piperidine-1-carboxamide

Example 6: rac-4-(5-cyclopropyl-1,2-oxazol-3-yl)-4-methyl-N-{(1S,2S)-2-[4-(propan-2-yl)piperazin-1-yl]cyclopentyl}piperidine-1-carboxamide

Example 7: rac-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,2S)-3,3-difluoro-2-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 8: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(4-methylphenyl)piperidine-1-carboxamide

Example 9: rac-(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carboxylate

Example 10: rac-(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl 4-methyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)piperidine-1-carboxylate

Example 11: rac-(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl 4-(5-cyclopropyl-1,2-oxazol-3-yl)-4-methylpiperidine-1-carboxylate

Example 12: rac-(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-7-yl]cyclohexyl 4-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-4-methylpiperidine-1-carboxylate

Example 13: rac-(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl 4-(1-cyclopropyl-1H-1,2,4-triazol-3-yl)-4-methylpiperidine-1-carboxylate

Example 14: (1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carboxylate

Example 15: rac-4-(5-cyclopropyl-1,2-oxazol-3-yl)-4-methyl-N-{2-[6-(propan-2-yl)pyridin-3-yl]cyclohex-2-en-1-yl}piperidine-1-carboxamide

Example 16: rac-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methyl-N-{2-[6-(propan-2-yl)pyridin-3-yl]cyclohex-2-en-1-yl}piperidine-1-carboxamide

Example 17

rac-N-[(1S,2S)-2-(4-Ethylpiperazin-1-yl)cyclohexyl]-4-(4-methylphenyl)piperidine-1-carboxamide

[0514] ##STR00174##

[0515] To a mixture of Reference example 2 (73.7 mg), sodium acetate (18.9 mg), acetaldehyde (0.054 ml), and dichloromethane (2 mL) was added sodium triacetoxyborohydride (122 mg) at 0° C., and the mixture was warmed to room temperature and stirred for 1.5 hours. Water was added to the reaction mixture at 0° C., and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound (24 mg).

[0516] .sup.1H-NMR (CDCl.sub.3) δ: 1.02-1.12 (1H, m), 1.07 (3H, t, J=7.3 Hz), 1.14-1.41 (3H, m), 1.57-1.71 (3H, m), 1.75-1.96 (5H, m), 2.16-2.78 (15H, m), 2.78-2.90 (2H, m), 3.24-3.39 (1H, m), 4.05-4.18 (2H, m), 5.72 (1H, s), 7.09 (2H, d, J=7.9 Hz), 7.12 (2H, d, J=7.9 Hz).

Example 18

rac-4-(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methyl-N-{2-[1-(propan-2-yl)-1,2,3,6-tetrahydropyridin-4-yl]cyclohex-2-en-1-yl}piperidine-1-carboxamide

[0517] ##STR00175##

[0518] To a solution of Reference example 13 (13.5 mg) in chloroform (2 mL) was added hydrogen chloride/acetic acid solution (4 M, 0.198 mL), and the mixture was stirred at room temperature. After the reaction was terminated as judged by the consumption of the starting material, the reaction mixture was concentrated in vacuo. To the obtained residue were added sodium acetate (8.66 mg), acetone (0.058 mL), and chloroform (2 mL). To the mixture was added sodium triacetoxyborohydride (33.6 mg) at 0° C., and the mixture was warmed to room temperature and stirred. After the reaction was completed, water was added to the reaction mixture under ice temperature, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound (10 mg).

[0519] .sup.1H-NMR (CDCl.sub.3) δ: 1.07 (6H, d, J=6.1 Hz), 1.17-1.22 (4H, m), 1.23-1.32 (2H, m), 1.29 (3H, s), 1.43-1.66 (3H, m), 1.91-1.98 (1H, m), 2.08-2.26 (6H, m), 2.26-2.41 (1H, m), 2.50 (1H, ddd, J=11.2, 7.2, 4.8 Hz), 2.63-2.76 (2H, m), 2.97-3.13 (3H, m), 3.13-3.23 (1H, m), 3.52-3.63 (2H, m), 4.43 (1H, d, J=7.3 Hz), 4.63-4.69 (1H, m), 5.78-5.84 (1H, m), 5.85-5.91 (1H, m).

Example 19

rac-4-(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

[0520] ##STR00176##

[0521] To a mixture of Reference example 14 (84.6 mg) (Material A), triethylamine (0.318 mL), and chloroform (2 mL) was added triphosgene (27.1 mg) at 0° C., and the mixture was stirred at the same temperature for 40 minutes. To the reaction mixture was added Reference example 8 (66.7 mg) (Material B) at 0° C., and the mixture was stirred at room temperature for one hour. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: chloroform/methanol) to give the title compound (99.1 mg).

[0522] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (3H, d, J=6.0 Hz), 1.01 (3H, d, J 6.0 Hz), 1.17-1.22 (4H, m), 1.23-1.30 (1H, m), 1.30-1.48 (2H, m), 1.31 (3H, s), 1.57-1.70 (2H, m), 1.75-1.84 (1H, m), 1.89-1.97 (1H, m), 2.10-2.27 (4H, m), 2.32-2.53 (7H, m), 2.53-2.64 (1H, m), 2.68-2.78 (2H, m), 3.08 (1H, ddd, J=13.6, 10.7, 3.1 Hz), 3.16 (1H, ddd, J=13.6, 10.7, 3.1 Hz), 3.66 (1H, ddd, J=13.6, 4.7, 4.1 Hz), 3.77 (1H, ddd, J 13.6, 4.7, 4.1 Hz), 4.10-4.21 (1H, m), 4.54 (1H, d, J=7.3 Hz).

Examples 20 to 76

[0523] The compounds of Examples 20 to 76 shown in the table below were prepared in the same manner as Example 19, by using commercial compounds or Reference example compounds which correspond to Material A and Material B described in Example 19.

TABLE-US-00002 Ex- Structure Material A Material B ample Spectral data Reference Reference 20 example 14 example 20 [00177] [00178] [00179] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-1.19 (10H, m), 1.27 (3H, s), 1.30-1.74 (3H, m), 1.75-1.88 (3H, m), 1.89-1.97 (1H, m), 1.97-2.04 (1H, m), 2.05-2.27 (3H, m), 2.32-2.67 (8H, m), 2.69-2.81 (2H, m), 3.12-3.29 (2H, m), 3.57- 3.68 (1H, m), 3.68-3.80 (1H, m), 4.08-4.25 (1H, m), 4.54 (1H, d, J = 7.3 Hz), 5.77 (1H, s). Reference Reference 21 example 14 example 21 [00180] [00181] [00182] .sup.1H-NMR (CDCl.sub.3) δ: 0.93 (6H, d, J = 6.1 Hz), 1.22- 1.43 (2H, m), 1.45 (3H, s), 1.63-1.86 (4H, m), 1.89- 1.97 (1H, m), 2.11-2.22 (1H, m), 2.28-2.54 (10H, m), 2.68-2.78 (2H, m), 3.11-3.26 (2H, m), 3.76 (1H, ddd, J = 13.5, 4.1, 4.0 Hz), 3.84 (1H, ddd, J = 13.5, 4.1, 4.0 Hz), 4.09-4.22 (1H, m), 4.56 (1H, d, J = 7.3 Hz), 7.29-7.35 (2H, m), 7.47-7.53 (1H, m), 7.67- 7.72 (1H, m). Reference Reference 22 example 15′ example 20 [00183] [00184] [00185] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-0.98 (2H, m), 1.00-1.08 (2H, m), 1.13 (6H, d, J = 6.0 Hz), 1.28 (3H, s), 1.28- 1.47 (3H, m), 1.47-1.88 (5H, m), 1.90-2.25 (5H, m), 2.25-3.07 (8H, m), 3.13-3.03 (2H, m), 3.58-3.74 (2H, m), 4.07-4.23 (1H, m), 4.54 (1H, d, J = 8.0 Hz), 5.78 (1H, s). Reference Reference 23 example 15′ example 8 [00186] [00187] [00188] .sup.1H-NMR (CDCl.sub.3) δ: 0.97-1.16 (6H, m), 1.16-1.26 (4H, m), 1.26-1.44 (3H, m), 1.31 (3H, s), 1.47-1.75 (5H, m), 1.75-1.88 (2H, m), 1.88-2.03 (1H, m), 2.09-2.28 (4H, m), 2.28-3.01 (6H, m), 3.01-3.26 (2H, m), 3.58- 3.84 (2H, m), 4.06-4.26 (1H, m), 4.54 (1H, d, J = 8.0 Hz). Reference Reference 24 example 15 example 8 [00189] [00190] [00191] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (3H, d, J = 6.0 Hz), 1.01 (3H, d, J = 6.0 Hz), 1.17-1.22 (4H, m), 1.23-1.30 (1H, m), 1.30-1.48 (2H, m), 1.31 (3H, s), 1.57-1.70 (2H, m), 1.75-1.84 (1H, m), 1.89-1.97 (1H, m), 2.10-2.27 (4H, m), 2.32-2.53 (7H, m), 2.53-2.64 (1H, m), 2.68- 2.78 (2H, m), 3.08 (1H, ddd, J = 13.6, 10.7, 3.1 Hz), 3.16 (1H, ddd, J = 13.6, 10.7, 3.1 Hz), 3.66 (1H, ddd, J = 13.6, 4.7, 4.1 Hz), 3.77 (1H, ddd, J = 13.6, 4.7, 4.1 Hz), 4.10-4.21 (1H, m), 4.54 (1H, d, J = 7.3 Hz). Reference Reference 25 example 15 example 20 [00192] [00193] [00194] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-1.19 (10H, m), 1.27 (3H, s), 1.30-1.74 (3H, m), 1.75-1.88 (3H, m), 1.89-1.97 (1H, m), 1.97-2.04 (1H, m), 2.05-2.27 (3H, m), 2.32-2.67 (8H, m), 2.69-2.81 (2H, m), 3.12-3.29 (2H, m), 3.57- 3.68 (1H, m), 3.68-3.80 (1H, m), 4.08-4.25 (1H, m), 4.54 (1H, d, J = 7.3 Hz), 5.77 (1H, s). Reference Reference 26 example 14 example 22 [00195] [00196] [00197] .sup.1H-NMR (CDCl.sub.3) δ: 0.84-0.91 (4H, m), 1.02 (6H, d, J = 6.7 Hz), 1.20-1.31 (3H, m), 1.31-1.41 (2H, m), 1.45 (3H, s), 1.46-1.59 (3H, m), 1.66-1.85 (3H, m), 1.89-1.97 (1H, m), 2.10-2.22 (1H, m), 2.35-2.55 (7H, m), 2.55-2.66 (1H, m), 2.67-2.79 (2H, m), 2.98-3.13 (2H, m), 3.18 (1H, ddd, J = 13.8, 10.5, 3.6 Hz), 3.59 (1H, ddd, J = 13.8, 4.6, 3.6 Hz), 3.63-3.79 (2H, m), 4.10-4.22 (1H, m), 4.53 (1H, d, J = 7.9 Hz). Reference Reference 27 example 14 example 19 [00198] [00199] [00200] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (6H, d, J = 6.8 Hz), 1.28- 1.46 (2H, m), 1.32 (3H, s), 1.57-1.66 (2H, m), 1.74- 1.88 (6H, m), 1.89-1.97 (1H, m), 2.10-2.21 (1H, m), 2.22-2.31 (2H, m), 2.35-2.54 (9H, m), 2.54-2.63 (3H, m), 2.69-2.78 (2H, m), 3.09 (1H, ddd, J = 13.8, 10.5, 2.9 Hz), 3.17 (1H, ddd, J = 13.8, 10.5, 2.9 Hz), 3.65 (1H, ddd, J = 13.8, 4.1, 4.1 Hz), 3.79 (1H, ddd, J = 13.8, 4.1, 4.1 Hz), 4.08-4.22 (1H, m), 4.53 (1H, d, J = 7.9 Hz). Reference Reference 28 example 14 example 9 [00201] [00202] [00203] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (3H, d, J = 6.0 Hz), 1.00 (3H, d, J = 6.0 Hz), 1.20-1.43 (3H, m), 1.33 (3H, s), 1.39 (3H, t, J = 7.7 Hz), 1.61-1.74 (2H, m), 1.75- 1.86 (1H, m), 1.89-1.98 (1H, m), 2.10-2.21 (1H, m), 2.21-2.30 (2H, m), 2.34-2.54 (7H, m), 2.54-2.64 (1H, m), 2.70-2.78 (2H, m), 2.89 (2H, q, J = 7.7 Hz), 3.09 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.17 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.66 (1H, ddd, J = 13.6, 4.4, 4.4 Hz), 3.79 (1H, ddd, J = 13.6, 4.4, 4.4 Hz), 4.08-4.22 (1H, m), 4.53 (1H, d, J = 7.9 Hz). Reference Reference 29 example 14 example 27 [00204] [00205] [00206] .sup.1H-NMR (CDCl.sub.3) δ: 0.94-1.15 (10H, m), 1.16-1.47 (3H, m), 1.29 (3H, s), 1.52-1.87 (5H, m), 1.87-1.99 (1H, m), 2.10-2.22 (1H, m), 2.23-2.36 (2H, m), 2.37-2.92 (8H, m), 2.97-3.08 (1H, m), 3.08-3.19 (1H, m), 3.43- 3.65 (2H, m), 3.72-3.84 (1H, m), 4.07-4.23 (1H, m), 4.52 (1H, d, J = 7.9 Hz), 8.00 (1H, s). Reference Reference 30 example 14 example 23 [00207] [00208] [00209] .sup.1H-NMR (CDCl.sub.3) δ: 1.03 (6H, d, J = 6.1 Hz), 1.10- 1.21 (1H, m), 1.22-1.51 (9H, m), 1.54-1.86 (5H, m), 1.61 (3H, s), 1.89-1.98 (1H, m), 2.08-2.23 (3H, m), 2.32-2.55 (7H, m), 2.55-2.65 (1H, m), 2.68-2.79 (2H, m), 3.01-3.19 (2H, m), 3.66 (1H, ddd, J = 13.6, 4.4, 3.2 Hz), 3.78 (1H, ddd, J = 13.6, 4.4, 3.2 Hz), 4.09-4.23 (1H, m), 4.52 (1H, d, J = 7.3 Hz). Reference Reference 31 example 14 example 28 [00210] [00211] [00212] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (3H, d, J = 6.1 Hz), 1.01 (3H, d, J = 6.1 Hz), 1.11-1.18 (2H, m), 1.22-1.35 (4H, m), 1.30 (3H, s), 1.35-1.47 (1H, m), 1.62-1.75 (2H, m), 1.75-1.85 (1H, m), 1.88-1.97 (1H, m), 2.10-2.22 (1H, m), 2.31-2.62 (11H, m), 2.67-2.78 (2H, m), 3.01 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.10 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.65 (1H, ddd, J = 14.0, 4.3, 4.3 Hz), 3.79 (1H, ddd, J = 14.0, 4.3, 4.3 Hz), 4.08-4.22 (1H, m), 4.53 (1H, d, J = 7.3 Hz). Reference Commercial 32 example 14 product [00213] [00214] [00215] .sup.1H-NMR (CDCl.sub.3) δ: 1.01 (6H, d, J = 6.8 Hz), 1.21- 1.49 (2H, m), 1.62-1.88 (4H, m), 1.89-2.06 (3H, m), 2.10-2.23 (1H, m), 2.34-2.66 (8H, m), 2.70-2.83 (2H, m), 2.85-3.07 (3H, m), 4.05-4.30 (3H, m), 4.60 (1H, d, J = 8.0 Hz), 7.10-7.18 (2H, m), 7.62 (1H, ddd, J = 8.0, 8.0, 1.6 Hz), 8.52 (1H, dd, J = 4.8, 1.6 Hz). Reference Commercial 33 example 14 product [00216] [00217] [00218] .sup.1H-NMR (CDCl.sub.3) δ: 1.03 (6H, d, J = 6.4 Hz), 1.20- 1.53 (10H, m), 1.54-1.66 (4H, m), 1.66-1.86 (3H, m), 1.88-1.98 (1H, m), 2.08-2.24 (1H, m), 2.26-2.56 (6H, m), 2.56-2.69 (1H, m), 2.69-2.82 (2H, m), 3.20-3.51 (4H, m), 4.06-4.25 (1H, m), 4.52 (1H, d, J = 8.0 Hz). Reference Reference 34 example 14 example 24 [00219] [00220] [00221] .sup.1H-NMR (CDCl.sub.3) δ: 1.01-1.23 (10H, m), 1.23-1.46 (4H, m), 1.43 (3H, s), 1.60-1.74 (1H, m), 1.74-1.87 (3H, m), 1.92-2.03 (1H, m), 2.11-2.29 (3H, m), 2.31-2.40 (1H, m), 2.40-3.14 (8H, m), 3.26-3.38 (2H, m), 3.58- 3.71 (2H, m), 4.08-4.23 (1H, m), 4.52 (1H, d, J = 7.9 Hz). Reference Commercial 35 example 14 product [00222] [00223] [00224] .sup.1H-NMR (CDCl.sub.3) δ: 0.82-1.07 (3H, m), 1.03 (6H, d, J = 6.8 Hz), 1.07-1.49 (11H, m), 1.49-1.86 (6H, m), 1.89-1.99 (1H, m), 2.09-2.25 (1H, m), 2.34-2.56 (7H, m), 2.56-2.67 (1H, m), 2.67-2.87 (4H, m), 3.89-3.99 (1H, m), 4.05-4.27 (2H, m), 4.49 (1H, d, J = 8.0 Hz). Reference Commercial 36 example 14 product [00225] [00226] [00227] .sup.1H-NMR (CDCl.sub.3) δ: 0.99 (6H, d, J = 6.4 Hz), 1.21- 1.49 (2H, m), 1.61-2.00 (5H, m), 2.01-2.12 (2H, m), 2.12-2.24 (1H, m), 2.29-2.64 (8H, m), 2.68-2.81 (2H, m), 2.87-3.00 (1H, m), 3.00-3.14 (2H, m), 3.97-4.09 (1H, m), 4.09-4.29 (2H, m), 4.58 (1H, d, J = 8.0 Hz), 7.13 (1H, t, J = 4.8 Hz), 8.67 (2H, d, J = 4.8 Hz). Reference Commercial 37 example 14 product [00228] [00229] [00230] .sup.1H-NMR (CDCl.sub.3) δ: 1.03 (6H, d, J = 6.4 Hz), 1.22- 1.51 (2H, m), 1.59-1.90 (4H, m), 1.90-2.07 (3H, m), 2.10-2.24 (1H, m), 2.34-2.65 (8H, m), 2.69-2.82 (2H, m), 3.33-3.50 (2H, m), 3.92-4.10 (2H, m), 4.13-4.28 (1H, m), 4.64 (1H, d, J = 8.0 Hz), 5.30 (1H, bs), 7.23 (1H, ddd, J = 8.0, 8.0, 1.6 Hz), 7.32 (1H, dd, J = 8.0, 1.6 Hz), 7.71 (1H, ddd, J = 8.0, 8.0, 1.6 Hz), 8.51-8.55 (1H, m). Reference Commercial 38 example 14 product [00231] [00232] [00233] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (6H, d, J = 6.4 Hz), 1.22- 1.50 (2H, m), 1.61-1.77 (3H, m), 1.77-2.00 (4H, m), 2.11-2.24 (1H, m), 2.31-2.64 (8H, m), 2.65-2.82 (3H, m), 2.83-3.04 (2H, m), 4.02-4.13 (1H, m), 4.13-4.33 (2H, m), 4.60 (1H, d, J = 8.0 Hz), 7.17-7.24 (3H, m), 7.27-7.34 (2H, m). Reference Commercial 39 example 14 product [00234] [00235] [00236] .sup.1H-NMR (CDCl.sub.3) δ: 0.95 (6H, d, J = 6.4 Hz), 1.18- 1.48 (4H, m), 1.60-1.86 (5H, m), 1.87-1.98 (1H, m), 2.07-2.23 (3H, m), 2.25-2.55 (8H, m), 2.66-2.78 (2H, m), 3.28-3.62 (4H, m), 4.07-4.24 (1H, m), 4.54 (1H, d, J = 8.0 Hz), 7.16-7.24 (1H, m), 7.28-7.38 (4H, m). Reference Commercial 40 example 14 product [00237] [00238] [00239] .sup.1H-NMR (CDCl.sub.3) δ: 0.99 (6H, d, J = 6.4 Hz), 1.22- 1.49 (2H, m), 1.56-1.88 (5H, m), 1.89-2.00 (1H, m), 2.01-2.24 (3H, m), 2.29-2.61 (8H, m), 2.68-2.81 (2H, m), 3.30-3.47 (2H, m), 3.85-4.05 (2H, m), 4.11-4.27 (1H, m), 4.62 (1H, d, J = 8.0 Hz), 7.25-7.31 (1H, m), 7.36 (2H, t, J = 8.0 Hz), 7.48 (2H, d, J = 8.0 Hz). Reference Commercial 41 example 14 product [00240] [00241] [00242] .sup.1H-NMR (CDCl.sub.3) δ: 0.99 (6H, d, J = 6.0 Hz), 1.21- 1.49 (2H, m), 1.60-1.88 (5H, m), 1.88-1.97 (1H, m), 1.97-2.09 (2H, m), 2.10-2.23 (1H, m), 2.27-2.61 (8H, m), 2.66-2.80 (2H, m), 3.25-3.43 (2H, m), 3.84-4.03 (2H, m), 4.07-4.24 (1H, m), 4.61 (1H, d, J = 8.0 Hz), 7.37 (2H, d, J = 8.8 HZ), 7.41 (2H, d, J = 8.8 Hz). Reference Reference 42 example 14 example 31 [00243] [00244] [00245] .sup.1H-NMR (CDCl.sub.3) δ: 1.01 (6H, d, J = 6.1 Hz), 1.19- 1.47 (3H, m), 1.65 (3H, s), 1.67-1.84 (3H, m), 1.90- 1.97 (1H, m), 2.09-2.21 (1H, m), 2.36-2.53 (9H, m), 2.55-2.66 (1H, m), 2.70-2.80 (2H, m), 3.19-3.36 (2H, m), 3.66 (1H, ddd, J = 13.0, 4.1, 3.5 Hz), 3.76 (1H, ddd, J = 13.0, 4.1, 3.5 Hz), 4.11-4.26 (1H, m), 4.52 (1H, d, J = 7.3 Hz), 6.68 (1H, d, J = 8.3 Hz), 6.81 (1H, dd, J = 6.7, 5.5 Hz), 7.49-7.54 (1H, m), 8.10 (1H, dd, J = 5.5, 1.7 Hz). Reference Reference 43 example 15 example 28 [00246] [00247] [00248] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (3H, d, J = 6.1 Hz), 1.01 (3H, d, J = 6.1 Hz), 1.11-1.18 (2H, m), 1.22-1.35 (4H, m), 1.30 (3H, s), 1.35-1.47 (1H, m), 1.62-1.75 (2H, m), 1.75-1.85 (1H, m), 1.88-1.97 (1H, m), 2.10-2.22 (1H, m), 2.31-2.62 (11H, m), 2.67-2.78 (2H, m), 3.01 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.10 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.65 (1H, ddd, J = 14.0, 4.3, 4.3 Hz), 3.79 (1H, ddd, J = 14.0, 4.3, 4.3 Hz), 4.08-4.22 (1H, m), 4.53 (1H, d, J = 7.3 Hz). Reference Reference 44 example 15 example 24 [00249] [00250] [00251] .sup.1H-NMR (CDCl.sub.3) δ: 1.01-1.23 (10H, m), 1.23-1.46 (4H, m), 1.43 (3H, s), 1.60-1.74 (1H, m), 1.74-1.87 (3H, m), 1.92-2.03 (1H, m), 2.11-2.29 (3H, m), 2.31-2.40 (1H, m), 2.40-3.14 (8H, m), 3.26-3.38 (2H, m), 3.58- 3.71 (2H, m), 4.08-4.23 (1H, m), 4.52 (1H, d, J = 7.9 Hz). Reference Reference 45 example 14 example 29 [00252] [00253] [00254] .sup.1H-NMR (CDCl.sub.3) δ: 1.04-1.19 (6H, m), 1.21-1.47 (3H, m), 1.31 (3H, s), 1.53-1.87 (3H, m), 1.89-2.01 (1H, m), 2.10-2.23 (1H, m), 2.28-2.40 (2H, m), 2.40-2.74 (7H, m), 2.74-3.03 (3H, m), 3.05-3.22 (2H, m), 3.58- 3.77 (2H, m), 4.05-4.22 (1H, m), 4.14 (3H, s), 4.53 (1H, s). Reference Commercial 46 example 14 product [00255] [00256] [00257] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (6H, d, J = 6.4 Hz), 1.22- 1.49 (2H, m), 1.62-1.88 (2H, m), 1.88-2.01 (3H, m), 2.10-2.23 (1H, m), 2.23-2.66 (10H, m), 2.70-2.83 (2H, m), 3.20-3.43 (2H, m), 3.89-4.01 (1H, m), 4.06- 4.27 (2H, m), 4.62 (1H, d, J = 8.0 Hz), 7.20 (1H, ddd, J = 8.0, 4.8, 1.2 Hz), 7.55 (1H, dd, J = 8.0, 1.2 Hz), 7.72 (1H, ddd, J = 8.0, 8.0, 1.2 Hz), 8.51 (1H, d, J = 4.8 Hz). Reference Reference 47 example 14 example 26 [00258] [00259] [00260] .sup.1H-NMR (CDCl.sub.3) δ: 0.96-1.02 (2H, m), 0.99 (6H, d, J = 6.0 Hz), 1.05-1.16 (2H, m), 1.18-1.48 (3H, m), 1.28 (3H, s), 1.62-1.76 (3H, m), 1.89-1.99 (1H, m), 2.08-2.23 (3H, m), 2.24-2.32 (1H, m), 2.32-2.63 (8H, m), 2.68-2.80 (2H, m), 3.24 (1H, ddd, J = 13.1, 9.2, 3.7 Hz), 3.34 (1H, ddd, J = 13.1, 9.2, 3.7 Hz), 3.43-3.52 (1H, m), 3.57-3.67 (1H, m), 4.07-4.22 (1H, m), 4.54 (1H, d, J = 7.3 Hz), 6.63 (1H, s). Reference Reference 48 example 14 example 25 [00261] [00262] [00263] .sup.1H-NMR (CDCl.sub.3) δ: 0.68-0.78 (2H, m), 0.95-1.16 (8H, m), 1.22-1.50 (3H, m), 1.35 (3H, s), 1.62-1.86 (3H, m), 1.88-1.97 (1H, m), 1.97-2.08 (1H, m), 2.10-2.30 (3H, m), 2.32-2.66 (8H, m), 2.68-2.86 (2H, m), 3.23 (1H, ddd, J = 13.6, 9.6, 3.2 Hz), 3.32 (1H, ddd, J = 13.6, 9.6, 3.2 Hz), 3.55-3.66 (1H, m), 3.66-3.76 (1H, m), 4.08-4.23 (1H, m), 4.54 (1H, d, J = 7.3 Hz), 7.32 (1H, s). Reference Commercial 49 example 15 product [00264] [00265] [00266] .sup.1H-NMR (CDCl.sub.3) δ: 0.95 (6H, d, J = 6.4 Hz), 1.19- 1.47 (3H, m), 1.25 (3H, s), 1.61-1.85 (3H, m), 1.88- 1.97 (1H, m), 2.06-2.22 (3H, m), 2.28-2.53 (8H, m), 2.32 (3H, s), 2.67-2.76 (2H, m), 3.32 (1H, ddd, J = 11.6, 8.0, 3.6 Hz), 3.40-3.49 (2H, m), 3.56 (1H, ddd, J = 11.6, 8.0, 3.6 Hz), 4.09-4.22 (1H, m), 4.53 (1H, d, J = 7.8 Hz), 7.14 (2H, d, J = 8.2 Hz), 7.22 (2H, d, J = 8.2 Hz). Reference Commercial 50 example 14 product [00267] [00268] [00269] .sup.1H-NMR (CDCl.sub.3) δ: 0.99 (6H, d, J = 6.0 Hz), 1.21- 1.49 (2H, m), 1.62-1.89 (4H, m), 1.89-2.06 (3H, m), 2.09-2.23 (1H, m), 2.30 (3H, s), 2.34-2.63 (8H, m), 2.67-2.80 (2H, m), 2.80-3.06 (3H, m), 4.03-4.29 (3H, m), 4.59 (1H, d, J = 8.0 Hz), 7.04 (1H, d, J = 8.0 Hz), 7.42 (1H, dd, J = 8.0, 2.4 Hz), 8.34 (1H, d, J = 2.4 Hz). Reference Reference 51 example 14 example 41 [00270] [00271] [00272] .sup.1H-NMR (CDCl.sub.3) δ: 1.01 (6H, d, J = 6.8 Hz), 1.21- 1.48 (2H, m), 1.61-1.88 (4H, m), 1.88-2.04 (3H, m), 2.09-2.24 (1H, m), 2.31 (3H, s), 2.35-2.66 (8H, m), 2.69-2.81 (2H, m), 2.85-3.09 (2H, m), 3.10-3.23 (1H, m), 4.00-4.10 (1H, m), 4.10-4.33 (2H, m), 4.58 (1H, d, J = 8.0 Hz), 7.14 (1H, d, J = 11.2 Hz), 8.14 (1H, s). Reference Commercial 52 example 14 product [00273] [00274] [00275] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (6H, d, J = 6.4 Hz), 1.22- 1.50 (2H, m), 1.62-1.87 (4H, m), 1.90-2.06 (3H, m), 2.10-2.23 (1H, m), 2.33-2.65 (8H, m), 2.69-2.81 (2H, m), 2.85-3.06 (3H, m), 4.04-4.30 (3H, m), 4.59 (1H, d, J = 8.0 Hz), 7.15 (1H, dd, J = 8.4, 4.4 Hz), 7.33 (1H, ddd, J = 8.4, 8.4, 2.8 Hz), 8.38 (1H, d, J = 2.8 Hz). Reference Commercial 53 example 14 product [00276] [00277] [00278] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (6H, d, J = 6.4 Hz), 1.21- 1.49 (2H, m), 1.63-1.87 (4H, m), 1.88-2.03 (3H, m), 2.09-2.23 (1H, m), 2.34-2.64 (8H, m), 2.68-2.80 (2H, m), 2.80-3.06 (3H, m), 3.84 (3H, s), 4.03-4.29 (3H, m), 4.59 (1H, d, J = 8.0 Hz), 7.07 (1H, d, J = 8.4 Hz), 7.14 (1H, dd, J = 8.4, 2.8 Hz), 8.22 (1H, d, J = 2.8 Hz). Reference Commercial 54 example 14 product [00279] [00280] [00281] .sup.1H-NMR (CDCl.sub.3) δ: 0.99 (6H, d, J = 6.4 Hz), 1.21- 1.49 (2H, m), 1.60-1.99 (5H, m), 1.99-2.10 (2H, m), 2.10-2.22 (1H, m), 2.27 (3H, s), 2.30-2.63 (8H, m), 2.67-2.81 (2H, m), 2.85-3.11 (2H, m), 3.95-4.08 (1H, m), 4.09-4.26 (3H, m), 4.58 (1H, d, J = 8.0 Hz), 8.48 (2H, s). Reference Commercial 55 example 14 product [00282] [00283] [00284] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (6H, d, J = 6.4 Hz), 1.22- 1.50 (2H, m), 1.63-1.90 (4H, m), 1.90-2.06 (3H, m), 2.10-2.25 (1H, m), 2.31-2.65 (8H, m), 2.69-2.81 (2H, m), 2.89-3.08 (3H, m), 4.06-4.32 (3H, m), 4.60 (1H, d, J = 8.0 Hz), 7.29 (1H, d, J = 8.4 Hz), 7.86 (1H, d, J = 8.4, 2.4 Hz), 8.79 (1H, s). Reference Reference 56 example 15 example 32 [00285] [00286] [00287] .sup.1H-NMR (CDCl.sub.3) δ: 0.94 (6H, d, J = 6.1 Hz), 1.23- 1.47 (3H, m), 1.34 (3H, s), 1.67-1.86 (3H, m), 1.88- 1.97 (1H, m), 2.10-2.23 (3H, m), 2.31 (3H, s), 2.31- 2.52 (8H, m), 2.67-2.76 (2H, m), 3.36 (1H, ddd, J = 11.6, 8.0, 3.6 Hz), 3.40-3.52 (2H, m), 3.53-3.59 (1H, m), 4.07-4.23 (1H, m), 4.54 (1H, d, J = 7.9 Hz), 6.81-6.91 (2H, m), 7.11 (1H, dd, J = 7.6, 7.6 Hz). Reference Reference 57 example 15 example 30 [00288] [00289] [00290] .sup.1H-NMR (CDCl.sub.3) δ: 0.86-0.93 (2H, m), 0.94-1.07 (2H, m), 1.00 (3H, d, J = 6.4 Hz), 1.01 (3H, d, J = 6.4 Hz), 1.20-1.48 (3H, m), 1.30 (3H, s), 1.54-1.85 (3H, m), 1.89-1.97 (1H, m), 2.09-2.22 (1H, m), 2.31-2.54 (9H, m), 2.54-2.64 (1H, m), 2.68-2.79 (2H, m), 3.06 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.16 (1H, ddd, J = 13.8, 10.7, 3.1 Hz), 3.58-3.68 (1H, m), 3.74-3.84 (1H, m), 4.09-4.23 (2H, m), 4.53 (1H, d, J = 7.9 Hz). Reference Commercial 58 example 14 product [00291] [00292] [00293] .sup.1H-NMR (CDCl.sub.3) δ: 0.95 (6H, d, J = 6.4 Hz), 1.19- 1.47 (3H, m), 1.25 (3H, s), 1.61-1.85 (3H, m), 1.88- 1.97 (1H, m), 2.06-2.22 (3H, m), 2.28-2.53 (8H, m), 2.32 (3H, s), 2.67-2.76 (2H, m), 3.32 (1H, ddd, J = 11.6, 8.0, 3.6 Hz), 3.40-3.49 (2H, m), 3.56 (1H, ddd, J = 11.6, 8.0, 3.6 Hz), 4.09-4.22 (1H, m), 4.53 (1H, d, J = 7.8 Hz), 7.14 (2H, d, J = 8.2 Hz), 7.22 (2H, d, J = 8.2 Hz). Reference Reference 59 example 14 example 33 [00294] [00295] [00296] .sup.1H-NMR (CDCl.sub.3) δ: 0.92 (3H, d, J = 6.7 Hz), 0.93 (3H, d, J = 6.7 Hz), 1.22-1.46 (3H, m), 1.29 (3H, s), 1.64-1.85 (3H, m), 1.88-1.96 (1H, m), 2.06-2.22 (3H, m), 2.25-2.54 (8H, m), 2.66-2.76 (2H, m), 3.36 (1H, ddd, J = 11.2, 7.6, 3.6 Hz), 3.41-3.59 (3H, m), 4.08-4.22 (1H, m), 4.54 (1H, d, J = 7.9 Hz), 6.63 (1H, t, J = 56.5 Hz), 7.42 (2H, d, J = 8.5 Hz), 7.48 (2H, d, J = 7.9 Hz). Reference Reference 60 example 15 example 34 [00297] [00298] [00299] .sup.1H-NMR (CDCl.sub.3) δ: 0.95 (6H, d, J = 6.7 Hz), 1.23- 1.48 (2H, m), 1.52 (3H, s), 1.59-1.74 (1H, m), 1.74- 1.84 (1H, m), 1.89-1.98 (1H, m), 2.00-2.10 (2H, m), 2.10-2.20 (1H, m), 2.21-2.32 (2H, m), 2.32-2.58 (8H, m), 2.35 (3H, s), 2.69-2.80 (2H, m), 3.43 (1H, ddd, J = 13.1, 9.2, 3.7 Hz), 3.48-3.61 (3H, m), 4.09-4.23 (1H, m), 4.52 (1H, d, J = 7.3 Hz), 7.29-7.36 (2H, m), 7.51 (1H, s). Reference Commercial 61 example 16 product [00300] [00301] [00302] .sup.1H-NMR (CDCl.sub.3) δ: 0.95-1.14 (6H, m), 1.17-1.31 (2H, m), 1.24 (3H, s), 1.33-1.80 (5H, m), 1.80-1.88 (1H, m), 2.05-2.25 (3H, m), 2.32 (3H, s), 2.53-2.63 (1H, m), 2.63-2.73 (1H, m), 2.78-2.88 (1H, m), 2.89-3.14 (2H, m), 3.20-3.34 (3H, m), 3.34-3.54 (3H, m), 3.84- 3.98 (2H, m), 4.22-4.37 (1H, m), 4.61 (1H, d, J = 8.5 Hz), 7.15 (2H, d, J = 8.5 Hz), 7.20 (2H, d, J = 8.5 Hz). Reference Reference 62 example 17 example 8 [00303] [00304] [00305] .sup.1H-NMR (CDCl.sub.3) δ: 0.89 (3H, d, J = 6.0 Hz), 0.90 (3H, d, J = 6.0 Hz), 1.15-1.22 (4H, m) 1.22-1.35 (1H, m), 1.29 (3H, s), 1.35-1.44 (1H, m), 1.44-1.53 (1H, m), 1.61-1.70 (3H, m), 1.70-1.85 (5H, m), 2.04-2.19 (3H, m), 2.20-2.29 (3H, m), 2.41-2.57 (4H, m), 3.03- 3.19 (3H, m), 3.19-3.24 (1H, m), 3.68-3.83 (2H, m), 3.94-4.07 (1H, m), 4.72 (1H, d, J = 7.3 Hz). Reference Commercial 63 example 17 product [00306] [00307] [00308] .sup.1H-NMR (CDCl.sub.3) δ: 0.84 (3H, d, J = 6.8 Hz), 0.85 (3H, d, J = 6.8 Hz), 1.19-1.35 (1H, m), 1.24 (3H, s), 1.35-1.43 (1H, m), 1.43-1.53 (1H, m), 1.59-1.85 (7H, m), 2.02-2.18 (4H, m), 2.21-2.27 (1H, m), 2.32 (3H, s), 2.34-2.59 (5H, m), 3.03-3.09 (1H, m), 3.18-3.25 (1H, m), 3.34-3.45 (2H, m), 3.46-3.59 (2H, m), 3.94- 4.08 (1H, m), 4.73 (1H, d, J = 7.3 Hz), 7.13 (2H, d, J = 7.9 Hz), 7.21 (2H, d, J = 7.9 Hz). Reference Reference 64 example 38 example 8 [00309] [00310] [00311] .sup.1H-NMR (CDCl.sub.3) δ: 1.06 (6H, d, J = 6.0 Hz), 1.18- 1.24 (4H, m), 1.30 (3H, s), 1.35-1.48 (2H, m), 1.56- 1.68 (2H, m), 1.68-1.78 (3H, m), 1.93-2.27 (6H, m), 2.31-2.41 (2H, m), 2.46-2.58 (1H, m), 2.63-2.72 (1H, m), 2.92-3.24 (4H, m), 3.63-3.75 (2H, m), 4.08-4.28 (2H, m), 4.51-4.60 (1H, m). Reference Reference 65 example 17 example 20 [00312] [00313] [00314] .sup.1H-NMR (CDCl.sub.3) δ: 0.88 (3H, d, J = 6.4 Hz), 0.89 (3H, d, J = 6.4 Hz), 0.91-0.99 (2H, m), 0.99-1.07 (2H, m), 1.20-1.35 (1H, m), 1.25 (3H, s), 1.35-1.42 (1H, m), 1.42-1.53 (1H, m), 1.58-1.84 (8H, m), 1.95-2.03 (1H, m), 2.03-2.16 (4H, m), 2.24-2.29 (1H, m), 2.41- 2.57 (4H, m), 3.04-3.10 (1H, m), 3.10-3.30 (3H, m), 3.67 (1H, ddd, J = 13.6, 4.5, 4.5 Hz), 3.75 (1H, ddd, J = 13.6, 4.5, 4.5 Hz), 3.93-4.07 (1H, m), 4.72 (1H, d, J = 7.3 Hz), 5.75 (1H, s). Reference Reference 66 example 15 example 11 [00315] [00316] [00317] .sup.1H-NMR (DMSO-d6) δ: 0.87 (6H, d, J = 6.4 Hz), 1.18- 1.36 (2H, m), 1.26 (3H, s), 1.47-1.66 (3H, m), 1.66- 1.88 (4H, m), 1.95-2.11 (3H, m), 2.17-2.40 (6H, m), 2.43-2.63 (5H, m), 2.95-3.19 (2H, m), 3.55-3.77 (2H, m), 3.98-4.18 (1H, m), 5.16 (1H, dddd, J = 65.0, 6.0, 6.0, 3.2 Hz), 5.88 (1H, d, J = 8.0 Hz). Reference Commercial 67 example 38 product [00318] [00319] [00320] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (6H, d, J = 7.3 Hz), 1.21- 1.30 (1H, m), 1.25 (3H, s), 1.35-1.48 (2H, m), 1.65- 1.84 (3H, m), 1.98-2.19 (6H, m), 2.25-2.36 (2H, m), 2.32 (3H, s), 2.48 (1H, dd, J = 16.4, 8.0 Hz), 2.59- 2.69 (1H, m), 2.94 (1H, dd, J = 10.1, 6.4 Hz), 3.14- 3,23 (1H, m), 3.27-3.42 (2H, m), 3.42-3.56 (2H, m), 4.07-4.28 (2H, m), 4.56 (1H, d, J = 9.2 Hz), 7.14 (2H, d, J = 8.2 Hz), 7.21 (2H, d, J = 8.2 Hz). Reference Reference 68 example 15 example 12′ [00321] [00322] [00323] .sup.1H-NMR (CDCl.sub.3) δ: 0.95-1.06 (8H, m), 1.13 (3H, d, J = 6.0 Hz), 1.21-1.57 (7H, m), 1.58-1.73 (2H, m), 1.73-1.87 (1H, m), 1.87-1.98 (1H, m), 2.08-2.30 (4H, m), 2.31-2.66 (8H, m), 2.66-2.83 (2H, m), 3.01-3.19 (2H, m), 3.61-3.72 (1H, m), 3.74-3.85 (1H, m), 4.03- 4.24 (1H, m), 4.53 (1H, d, J = 8.0 Hz). Reference Reference 69 example 15 example 12 [00324] [00325] [00326] .sup.1H-NMR (CDCl.sub.3) δ: 0.97-1.06 (8H, m), 1.13 (3H, d, J = 6.4 Hz), 1.22-1.58 (7H, m), 1.58-1.73 (2H, m), 1.73-1.87 (1H, m), 1.89-1.99 (1H, m), 2.08-2.30 (4H, m), 2.31-2.66 (8H, m), 2.66-2.84 (2H, m), 3.00-3.22 (2H, m), 3.61-3.72 (1H, m), 3.74-3.85 (1H, m), 4.03- 4.23 (1H, m), 4.53 (1H, d, J = 8.0 Hz). Reference Commercial 70 example 15 product [00327] [00328] [00329] .sup.1H-NMR (CDCl.sub.3) δ: 0.97-1.04 (6H, m), 1.20-1.48 (7H, m), 1.62-1.87 (3H, m), 1.89-1.98 (1H, m), 2.10-2.21 (1H, m), 2.21-2.31 (2H, m) 2.31-2.54 (6H, m) 2.58 (1H, sept, J = 6.4 Hz), 2.68-2.80 (2H, m), 3.10 (1H, ddd, J = 12.8, 10.0, 2.4 Hz), 3.17 (1H, ddd, J = 13.2, 10.4, 2.8 Hz), 3.63-3.73 (1H, m) 3.73-3.83 (3H, m), 4.08-4.23 (1H, m), 4.54 (1H, d, J = 8.0 Hz). Reference Reference 71 example 37 example 8 [00330] [00331] [00332] .sup.1H-NMR (CDCl.sub.3) δ: 1.05 (3H, d, J = 6.4 Hz), 1.06 (3H, d, J = 6.4 Hz), 1.17-1.23 (4H, m), 1.30 (3H, s), 1.36-1.47 (2H, m), 1.56-1.81 (5H, m), 1.98 (1H, ddd, J = 16.0, 13.6, 8.0 Hz), 2.03-2.26 (5H, m), 2.31- 2.42 (2H, m), 2.51 (1H, dd, J = 16.0, 8.0 Hz), 2.60- 2.67 (1H, m), 2.97 (1H, dd, J = 10.1, 6.4 Hz), 3.04- 3.23 (3H, m), 3.63-3.75 (2H, m), 4.07-4.27 (2H, m), 4.55 (1H, d, J = 9.2 Hz). Reference Reference 72 example 37 example 11 [00333] [00334] [00335] .sup.1H-NMR (CDCl.sub.3) δ: 1.04 (3H, d, J = 6.0 Hz), 1.05 (3H, d, J = 6.0 Hz), 1.33 (3H, s), 1.35-1.53 (3H, m), 1.57-1.82 (5H, m), 1.90-2.03 (2H, m), 2.03-2.20 (2H, m), 2.21-2.30 (2H, m), 2.30-2.41 (3H, m), 2.50 (1H, dd, J = 18.4, 8.4 Hz), 2.64 (1H, ddd, J = 8.5, 8.4, 4.6 Hz), 2.98 (1H, dd, J = 10.1, 6.4 Hz), 3.03-3.25 (3H, m), 3.65-3.75 (2H, m), 4.06-4.27 (2H, m), 4.55 (1H, d, J = 9.1 Hz), 4.91 (1H, dddd, J = 63.7, 6.4, 6.4, 4.0 Hz). Reference Reference 73 example 38 example 11 [00336] [00337] [00338] .sup.1H-NMR (CDCl.sub.3) δ: 1.61 (6H, d, J = 6.4 Hz), 1.89 (3H, s), 1.92-2.10 (3H, m), 2.15-2.41 (5H, m), 2.47-2.77 (4H, m), 2.78-2.86 (2H, m), 2.86-2.97 (3H, m), 3.01- 3.13 (1H, m), 3.17-3.27 (1H, m), 3.53 (1H, ddd, J = 19.8, 9.9, 6.5 Hz), 3.59-3.81 (3H, m), 4.20-4.34 (2H, m), 4.64-4.86 (2H, m), 5.07-5.17 (1H, m), 5.48 (1H, dddd, J = 63.7, 6.0, 6.0, 3.6 Hz). Reference Reference 74 example 37 example 12 [00339] [00340] [00341] .sup.1H-NMR (CDCl.sub.3) δ: 1.06-1.12 (1H, m), 1.13 (3H, d, J = 6.1 Hz), 1.24-1.38 (11H, m), 1.39-1.55 (3H, m), 1.56-1.66 (2H, m), 1.67-1.79 (1H, m), 1.93-2.02 (1H, m), 2.04-2.19 (311, m), 2.19-2.28 (3H, m), 2.78-2.81 (1H, m), 2.88 (1H, ddd, J = 10.4, 10.4, 6.8 Hz), 3.02-3.19 (3H, m), 3.20-3.36 (2H, m), 3.56-3.73 (3H, m), 4.12-4.28 (2H, m), 4.74 (1H, d, J = 9.2 Hz). Reference Reference 75 example 39 example 8 [00342] [00343] [00344] .sup.1H-NMR (CDCl.sub.3) δ: 1.01-1.09 (6H, m), 1.17-1.23 (4H, m), 1.30 (3H, s), 1.37-1.50 (2H, m), 1.55-1.67 (2H, m), 1.67-1.81 (2H, m), 2.05-2.27 (6H, m), 2.32-2.42 (1H, m), 2.54-2.69 (1H, m), 2.93-3.36 (5H, m), 3.63- 3.76 (2H, m), 4.06-4.31 (2H, m), 4.59-4.68 (1H, m), 4.76-4.96 (1H, m). Reference Reference 76 example 40 example 8 [00345] [00346] [00347] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (3H, d, J = 6.1 Hz), 1.04 (3H, d, J = 6.7 Hz), 1.17-1.23 (4H, m), 1.30 (3H, s), 1.32-1.51 (2H, m), 1.58-1.70 (2H, m), 1.71-1.87 (2H, m), 2.11-2.26 (5H, m), 2.35-2.50 (2H, m), 2.61-2.74 (1H, m), 3.04-3.27 (4H, m), 3.41-3.50 (1H, m), 3.62- 3.75 (2H, m), 4.00-4.10 (1H, m), 4.19-4.32 (1H, m), 4.64 (1H, d, J = 8.5 Hz).

[0524] The chemical names of Example 20 to Example 76 are listed below.

Example 20: rac-4-(5-cyclopropyl-1,2-oxazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 21: rac-4-(1,3-benzoxazol-2-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 22: 4-(5-cyclopropyl-1,2-oxazol-3-yl)-N-{(1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 23: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 24: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 25: 4-(5-cyclopropyl-1,2-oxazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 26: rac-4-cyclopentyl-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 27: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-(4,5,6,7-tetrahydro-1,3-benzoxazol-2-yl)piperidine-1-carboxamide

Example 28: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(5-ethyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carboxamide

Example 29: rac-4-(l-cyclopropyl-?H-1,2,4-triazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 30: rac-4-(4,4-difluorocyclohexyl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 31: rac-4-(5-cyclopropyl-1,2,4-thiadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 32: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(pyridin-2-yl)piperidine-1-carboxamide

Example 33: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-8-azaspiro[4.5]decane-8-carboxamide

Example 34: rac-4-(5-cyclopropyl-1,3,4-thiadiazol-2-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 35: rac-4-cyclohexyl-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}piperidine-1-carboxamide

Example 36: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(pyrimidin-2-yl)piperidine-1-carboxamide

Example 37: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-hydroxy-4-(pyridin-2-yl)piperidine-1-carboxamide

Example 38: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-phenylpiperidine-1-carboxamide

Example 39: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-phenylpiperidine-1-carboxamide

Example 40: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-hydroxy-4-phenylpiperidine-1-carboxamide

Example 41: rac-4-(4-chlorophenyl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-hydroxypiperidine-1-carboxamide

Example 42: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-[(pyridin-2-yl)oxy]piperidine-1-carboxamide

Example 43: 4-(5-cyclopropyl-1,2,4-thiadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 44: 4-(5-cyclopropyl-1,3,4-thiadiazol-2-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 45: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(5-methoxy-1,2,4-thiadiazol-3-yl)-4-methylpiperidine-1-carboxamide

Example 46: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-fluoro-4-(pyridin-2-yl)piperidine-1-carboxamide

Example 47: rac-4-(2-cyclopropyl-1,3-thiazol-4-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 48: rac-4-(5-cyclopropyl-1,3-thiazol-2-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 49: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide

Example 50: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(5-methylpyridin-2-yl)piperidine-1-carboxamide

Example 51: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(3-fluoro-5-methylpyridin-2-yl)piperidine-1-carboxamide

Example 52: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(5-fluoropyridin-2-yl)piperidine-1-carboxamide

Example 53: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(5-methoxypyridin-2-yl)piperidine-1-carboxamide

Example 54: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(5-methylpyrimidin-2-yl)piperidine-1-carboxamide

Example 55: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-[5-(trifluoromethyl)pyridin-2-yl]piperidine-1-carboxamide

Example 56: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-(2-fluoro-4-methylphenyl)-4-methylpiperidine-1-carboxamide

Example 57: 4-[5-(cyclopropyloxy)-1,2,4-thiadiazol-3-yl]-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 58: rac-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide

Example 59: rac-4-[4-(difluoromethyl)phenyl]-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 60: 4-(2-cyano-4-methylphenyl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 61: N-{(1R,6S)-2,2-difluoro-6-[6-(propan-2-yl)-3,6-diazabicyclo[3.1.1]heptan-3-yl]cyclohexyl}-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide

Example 62: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[3-(propan-2-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 63: N-{(1R,6S)-2,2-difluoro-6-[3-(propan-2-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl]cyclohexyl}-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide

Example 64: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 65: 4-(5-cyclopropyl-1,2-oxazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[3-(propan-2-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 66: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 67: N-[(1R,6S)-2,2-difluoro-6-{[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide

Example 68: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-{5-[(1S,2R)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide

Example 69: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-{5-[(1R,2S)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide

Example 70: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methyl-4-[5-(2,2,2-trifluoroethyl)-1,2,4-oxadiazol-3-yl]piperidine-1-carboxamide

Example 71: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 72: N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 73: N-[(1R,6S)-2,2-difluoro-6-{[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 74: N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methyl-4-{5-[(1R,2S)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide

Example 75: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S,4S)-4-fluoro-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 76: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-6-{[(3R)-4,4-difluoro-1-(propan-2-yl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-methylpiperidine-1-carboxamide

Example 77

rac-N-{(1R,6S)-2,2-Difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4′-methyl-1,2,3,6-tetrahydro[1,1′-biphenyl]-4-carboxamide

[0525] ##STR00348##

[0526] To a solution of 4-(4-methylphenyl)-cyclohex-1-ene-carboxylic acid (64.3 mg) in chloroform (2 mL) were added oxalyl chloride (0.036 mL) and DMF (5 μL), and the mixture was stirred at room temperature for 3 hours. Then, the reaction solution was concentrated in vacuo, and chloroform (2 mL), triethylamine (0.120 mL), and Reference example 14 (53.3 mg) were added to the reaction residue. The mixture was stirred. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound (55.6 mg).

[0527] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (6H, d, J=6.7 Hz), 1.23-1.50 (2H, m), 1.71-1.91 (4H, m), 1.93-2.11 (2H, m), 2.13-2.68 (14H, m), 2.69-2.89 (4H, m), 4.27-4.44 (1H, m), 5.68-5.77 (1H, m), 6.67-6.77 (1H, m), 7.09-7.20 (4H, m).

Example 78

rac-(1R,6S)-2,2-Difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl 4′-methyl-1,2,3,6-tetrahydro[1,1′-biphenyl]-4-carboxylate

[0528] The compound of Example 78 shown in the table below was prepared in the same manner as Example 77, by using Reference example 6 instead of Reference example 14 in Example 77.

TABLE-US-00003 Example Structure Instrumental analytical data 78 [00349] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (3H, d, J = 6.0 Hz), 1.03 (3H, d, J = 6.0 Hz), 1.29-1.53 (2H, m), 1.58-1.85 (4H, m), 1.88-1.97 (1H, m), 1.98-2.08 (1H, m), 2.14-2.25 (1H, m), 2.25-2.53 (11H, m), 2.53-2.66 (2H, m), 2.67-2.83 (4H, m), 5.04-5.16 (1H, m), 7.09-7.16 (5H, m).

Example 79

rac-4-(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carbothioamide

[0529] ##STR00350##

[0530] To a mixture of Reference example 14 (10.0 mg) (Material A), N,N-diisopropylamine (0.034 mL), and chloroform (0.2 mL) was added thiophosgene (4.40 mg) at 0° C., and the mixture was stirred at the same temperature for 40 minutes. To the reaction mixture was added Reference example 8 (66.7 mg)(Material B) at 0° C., and the mixture was stirred at room temperature for one hour. The mixture was directly purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound (9.6 mg).

[0531] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (6H, d, J=5.6 Hz), 1.14-1.27 (4H, m), 1.27-1.50 (2H, m), 1.50-1.91 (8H, m), 1.91-2.04 (1H, m), 2.08-2.24 (2H, m), 2.24-2.35 (2H, m), 2.35-2.55 (5H, m), 2.55-2.70 (2H, m), 2.79-3.00 (2H, m), 3.33 (1H, t, J=11.2 Hz), 3.49 (1H, t, J=11.2 Hz), 4.16 (1H, d, J=12.8 Hz), 4.49 (1H, d, J=12.8 Hz), 5.02-5.26 (1H, m), 5.42 (1H, d, J=8.0 Hz).

Example 80

4-(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carbothioamide

[0532] The compound of Example 80 shown in the table below was prepared in the same manner as Example 79, by using Reference example 15 corresponding to Material A in Example 79 and Reference example 8 corresponding to Material B in Example 79.

TABLE-US-00004 Structure Material A Material B Example Spectral data Reference Reference 80 example 15 example 8 [00351] [00352] [00353] .sup.1H-NMR (CDCl.sub.3) δ: 1.02 (6H, d, J = 5.6 Hz), 1.14- 1.27 (4H, m), 1.27-1.50 (2H, m), 1.50-1.91 (8H, m), 1.91-2.04 (1H, m), 2.08-2.24 (2H, m), 2.24-2.35 (2H, m), 2.35-2.55 (5H, m), 2.55-2.70 (2H, m), 2.79-3.00 (2H, m), 3.33 (1H, t, J = 11.2 Hz), 3.49 (1H, t, J = 11.2 Hz), 4.16 (1H, d, J = 12.8 Hz), 4.49 (1H, d, J = 12.8 Hz), 5.02-5.26 (1H, m), 5.42 (1H, d, J = 8.0 Hz).

Example 81

rac-4-(4-Methylphenyl)-N-[(1S,4R)-3-{[4-(propan-2-yl)piperazin-1-yl]methyl}bicyclo[2.2.1]heptan-2-yl]piperidine-1-carboxamide

[0533] ##STR00354##

[0534] To a solution of Reference example 40 (20 mg) in chloroform (0.5 mL) was added TFA (0.057 ml) at room temperature, and the mixture was stirred at the same temperature for one hour. The reaction solution was concentrated in vacuo, and the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate). The obtained residue was dissolved in chloroform (0.284 mL). To the solution were added N,N-diisopropylethylamine (36.8 mg) and triphosgene (8.4 mg) at 0° C., and the mixture was stirred at the same temperature for one hour. Then, 4-(4-methylphenyl)piperidine (0.057 mL) was added to the reaction mixture, which was stirred at room temperature for one hour. The reaction mixture was directly purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound (8 mg).

[0535] .sup.1H-NMR (CDCl.sub.3) δ: 1.24 (6H, d, J=7.3 Hz), 1.31-1.49 (7H, m), 1.54-1.67 (4H, m), 1.84 (2H, m), 2.24 (1H, m), 2.32 (3H, s), 2.63 (2H, m), 2.80-2.99 (4H, m), 3.06-3.49 (8H, m), 4.05-4.14 (3H, m), 7.07-7.13 (4H, m).

Examples 82-156

[0536] The compounds of Examples 82 to 156 shown in the table below were prepared in the same manner as Example 19, by using commercial compounds or Reference example compounds which correspond to Material A and Material B described in Example 19.

TABLE-US-00005 Structure Material A Material B Example Spectral data Reference Reference 82 example 58 example 116 [00355] [00356] [00357] .sup.1H-NMR (DMSO-d6) δ: 0.87 (6H, d, J = 6.4 Hz), 1.18- 1.36 (2H, m), 1.26 (3H, s), 1.47-1.66 (3H, m), 1.66- 1.88 (4H, m), 1.95-2.11 (3H, m), 2.17-2.40 (6H, m), 2.43-2.63 (5H, m), 2.95-3.19 (2H, m), 3.55-3.77 (2H, m), 3.98-4.18 (1H, m), 5.16 (1H, dddd, J = 65.0, 6.0, 6.0, 3.2 Hz), 5.88 (1H, d, J = 8.0 Hz). Reference Reference 83 example 96 example 115 [00358] [00359] [00360] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (5H, d, J = 6.4 Hz), 1.13 d, J = 6.4 Hz), 1.33 (3H, s), 1.38-1.85 (9H, m), 1.90-2.30 (8H, m), 2.32-2.41 (1H, m), 2.60-2.74 (4H, m), 3.03-3.15 (2H, m), 3.17-3.28 (1H, m), 3.33-3.44 (1H, m), 3.65-3.76 (2H, m), 4.13-4.30 (1H, m), 4.51 (1H, d, J = 9.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 84 example 96 example 8 [00361] [00362] [00363] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (6H, dd, J = 6.8, 1.2 Hz), 1.17-1.25 (4H, m), 1.30 (3H, s), 1.38-1.46 (2H, m), 1.50-1.69 (4H, m), 1.69-1.85 (4H, m), 2.00-2.30 (7H, m), 2.60-2.74 (3H, m), 3.03-3.15 (2H, m), 3.17-3.28 (1H, m), 3.33-3.42 (1H, m), 3.64-3.74 (2H, m), 4.13- 4.30 (1H, m), 4.50 (1H, d, J = 9.2 Hz). Reference Reference 85 example 91 example 8 [00364] [00365] [00366] .sup.1H-NMR (CDCl.sub.3) δ: 1.16-1.23 (4H, m), 1.27 (3H, s), 1.36 (6H, d, J = 6.8 Hz), 1.44-1.58 (2H, m), 1.58- 1.75 (1H, m), 1.80-2.06 (4H, m), 2.09-2.23 (3H, m), 2.23-2.35 (1H, m), 2.88-3.08 (3H, m), 3.11-3.25 (1H, m), 3.48-3.67 (2H, m), 4.41-4.57 (1H, m), 4.57-4.67 (1H, m). Reference Reference 86 example 91 example 115 [00367] [00368] [00369] .sup.1H-NMR (CDCl.sub.3) δ: 1.30 (3H, s), 1.35 (6H, d, J = 6.4 Hz), 1.42-1.62 (3H, m), 1.62-7.75 (1H, m), 1.80-2.07 (5H, m), 2.11-2.22 (2H, m), 2.22-2.41 (2H, m), 2.89- 3.08 (3H, m), 3.11-3.24 (1H, m), 3.50-3.66 (2H, m), 4.41-4.56 (1H, m), 4.58-4.67 (1H, m), 4.93 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 87 example 97 example 115 [00370] [00371] [00372] .sup.1H-NMR (CDCl.sub.3) δ: 1.25 (3H, s), 1.26-1.37 (1H, m), 1.30 (3H, d, J = 6.4 Hz), 1.31 (3H, d, J = 6.4 Hz), 1.39-1.74 (4H, m), 1.74-2.01 (3H, m), 2.10-2.19 (2H, m), 2.19-2.30 (1H, m), 2.30-2.39 (2H, m), 2.86 (1H, ddd, J = 14.0, 11.0, 3.1 Hz), 2.96-3.08 (2H, m), 3.41-3.50 (1H, m), 3.63-3.72 (1H, m), 4.46-4.60 (1H, m), 4.78-4.86 (1H, m), 4.41 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz), 5.06-5.15 (1H, m). Reference Reference 88 example 98 example 115 [00373] [00374] [00375] .sup.1H-NMR (CDCl.sub.3) δ: 1.30 (3H, s), 1.41-1.89 (14H, m), 1.90-2.02 (1H, m), 2.13-2.30 (4H, m), 2.31-2.41 (1H, m), 2.99-3.13 (2H, m), 3.60-3.78 (2H, m), 4.32-4.50 (2H, m), 4.63 (1H, d, J = 9.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz), 7.17 (1H, s), 7.21 (1H, s). Reference Reference 89 example 99 example 115 [00376] [00377] [00378] .sup.1H-NMR (CDCl.sub.3) δ: 1.13 (6H, d, J = 6.0 Hz), 1.32 (3H, s), 1.42-1.83 (5H, m), 1.87-2.04 (2H, m), 2.06-2.17 (2H, m), 2.18-2.28 (4H, m), 2.31-2.41 (1H, m), 2.60- 2.73 (1H, m), 2.88-3.17 (5H, m), 3.30-3.80 (6H, m), 4.80-5.04 (1H, m). Reference Reference 90 example 98 example 8 [00379] [00380] [00381] .sup.1H-NMR (CDCl.sub.3) δ: 1.17-1.23 (4H, m), 1.27 (3H, s), 1.44 (3H, d, J = 6.7 Hz), 1.45 (3H, d, J = 6.7 Hz), 1.46-1.65 (4H, m), 1.69-1.91 (2H, m), 2.12-2.30 (5H, m), 2.99-3.12 (2H, m), 3.59-3.69 (2H, m), 3.69-3.77 (1H, m), 4.31-4.50 (2H, m), 4.63 (1H, d, J = 9.2 Hz), 7.16 (1H, s), 7.20 (1H, s). Reference Reference 91 example 89 example 115 [00382] [00383] [00384] .sup.1H-NMR (CDCl.sub.3) δ: 1.09-1.43 (11H, m), 1.43-1.56 (2H, m), 1.56-1.76 (3H, m), 1.76-2.24 (7H, m), 2.24-2.48 (5H, m), 2.48-2.75 (1H, m), 2.75-3.06 (1H, m), 3.06- 3.45 (4H, m), 3.45-3.71 (1H, m), 3.71-3.87 (1H, m), 3.87-4.13 (1H, m), 4.13-4.50 (1H, m), 4.94 (1H, dddd, J = 64.4, 6.0, 6.0, 4.0 Hz), 7.13-7.44 (5H, m), 11.97 (1H, brs). Reference Reference 92 example 119 example 115 [00385] [00386] [00387] .sup.1H-NMR (CDCl.sub.3) δ: 1.18-1.29 (1H, m), 1.22 (3H, s), 1.30 (3H, d, J = 6.4 Hz), 1.31 (3H, d, J = 6.4 Hz), 1.40-1.53 (3H, m), 1.58-1.71 (1H, m), 1.78-2.03 (3H, m), 2.05-2.12 (2H, m), 2.17-2.28 (1H, m), 2.30-2.40 (2H, m), 2.81 (1H, ddd, J = 13.6, 10.8, 2.9 Hz), 2.93-3.06 (2H, m), 3.37-3.47 (1H, m), 3.54-3.61 (1H, m), 4.41-4.54 (1H, m), 4.74 (1H, d, J = 9.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz), 5.40-5.48 (1H, m), 6.53 (1H, d, J = 5.5 Hz), 8.35 (1H, d, J = 5.5 Hz). Reference Reference 93 example 92 example 115 [00388] [00389] [00390] .sup.1H-NMR (CDCl.sub.3) δ: 1.24-1.30 (9H, m), 1.35-1.53 (3H, m), 1.65-2.04 (6H, m), 2.07-2.20 (2H, m), 2.27-2.40 (2H, m), 2.83 (1H, ddd, J = 14.0, 11.6, 3.2 Hz), 2.95-3.10 (2H, m), 3.40-3.49 (1H, m), 3.57-3.67 (1H, m), 4.60-4.71 (3H, m), 4.90 (1H, dddd, J = 64.0, 6.0, 6.0, 4.0 Hz), 7.42 (1H, s). Reference Reference 94 example 93 example 115 [00391] [00392] [00393] .sup.1H-NMR (CDCl.sub.3) δ: 0.89 (6H, t, J = 6.8 Hz), 1.27 (3H, s), 1.36-1.53 (3H, m), 1.64-2.04 (6H, m), 2.07-2.20 (2H, m), 2.27-2.40 (3H, m), 2.48-2.63 (2H, m), 2.84 (1H, ddd, J = 14.0, 11.2, 3.2 Hz), 2.98 (1H, ddd, J = 14.0, 11.2, 3.2 Hz), 3.40-3.50 (1H, m), 3.54-3.65 (1H, m), 4.60-4.76 (3H, m), 4.90 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz), 7.43 (1H, s). Reference Reference 95 example 81 example 115 [00394] [00395] [00396] .sup.1H-NMR (CDCl.sub.3) δ: 1.00-1.11 (6H, m), 1.15-1.54 (7H, m), 1.54-1.75 (4H, m), 1.75-2.07 (5H, m), 2.15 (3H, s), 2.20-2.30 (3H, m), 2.30-2.42 (2H, m), 2.42-2.57 (1H, m), 2.59-2.70 (1H, m), 2.73-2.85 (1H, m), 2.90 (1H, t, J = 8.0 Hz), 3.02-3.18 (2H, m), 3.23 (1H, tt, J = 15.2, 7.2 Hz), 3.63-3.79 (2H, m), 4.07-4.22 (1H, m), 4.54 (1H, d, J = 7.6 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 96 example 59 example 115 [00397] [00398] [00399] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-1.02 (6H, m), 1.20-1.54 (6H, m), 1.54-2.03 (8H, m), 2.08 (3H, s), 2.10-2.27 (3H, m), 2.32-2.48 (2H, m), 2.60-2.70 (2H, m), 2.76-3.23 (6H, m), 3.62-3.77 (2H, m), 4.07-4.22 (1H, m), 4.53 (1H, d, J = 8.0 Hz), 4.91 (1H, dddd, J = 64.0, 6.4, 6.4, 3.6 Hz). Reference Reference 97 example 18 example 117 [00400] [00401] [00402] .sup.1H-NMR (CDCl.sub.3) δ: 1.00 (6H, d, J = 6.4 Hz), 1.22-1.48 (2H, m), 1.34 (3H, s), 1.49-1.60 (1H, m), 1.61-1.75 (2H, m), 1.75-1.87 (1H, m), 1.87-1.98 (1H, m), 1.98- 2.22 (3H, m), 2.22-2.33 (2H, m), 2.33-2.54 (11H, m), 2.54-2.64 (1H, m), 2.68-2.81 (2H, m), 3.14 (2H, dddd, J = 32.4, 14.0, 10.8, 3.2 Hz), 3.62-3.84 (3H, m), 4.16 (1H, dddd, J = 23.6, 11.2, 8.0, 3.6 Hz), 4.54 (1H, d, J = 8.0 Hz). Reference Reference 98 example 100 example 115 [00403] [00404] [00405] .sup.1H-NMR (CDCl.sub.3) δ: 1.00-1.11 (6H, m), 1.33 (3H, s), 1.36-1.84 (13H, m), 1.85-2.07 (4H, m), 2.07-2.20 (1H, m), 2.22-2.31 (2H, m), 2.31-2.41 (1H, m), 2.90 (1H, sep, J = 6.4 Hz), 3.03-3.26 (3H, m), 3.42-3.52 (2H, m), 3.59-3.78 (3H, m), 4.10-4.24 (1H, m), 4.50 (1H, d, J = 9.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 99 example 59 example 8 [00406] [00407] [00408] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-1.00 (6H, m), 1.13 (2H, d, J = 6.0 Hz), 1.17-1.24 (4H, m), 1.30 (3H, s), 1.32-1.50 (2H, m), 1.56-1.70 (2H, m), 1.70-1.86 (1H, m), 1.86- 1.97 (2H, m), 2.08 (3H, s), 2.11-2.26 (4H, m), 2.44 (1H, t, J = 7.6 Hz), 2.60-2.70 (2H, m), 2.76-2.86 (1H, m), 2.86-2.92 (2H, m), 2.92-3.17 (3H, m), 3.60- 3.77 (2H, m), 4.07-4.23 (1H, m), 4.53 (1H, d, J = 7.6 Hz). Reference Reference 100 example 101 example 115 [00409] [00410] [00411] .sup.1H-NMR (CDCl.sub.3) δ: 0.91-0.97 (6H, m), 1.32 (3H, s), 1.37-1.86 (11H, m), 1.90-2.04 (3H, m), 2.07-2.21 (2H, m), 2.21-2.41 (5H, m), 2.49 (1H, sep, J = 6.0 Hz), 2.62 (2H, dd, J = 15.6, 10.8 Hz), 3.02-3.16 (2H, m), 3.21-3.32 (1H, m), 3.59 (1H, t, J = 4.4 Hz), 3.63- 3.78 (2H, m), 4.22-4.37 (1H, m), 4.56 (1H, d, J = 8.8 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 4.0 Hz). Reference Reference 101 example 60 example 115 [00412] [00413] [00414] .sup.1H-NMR (CDCl.sub.3) δ: 1.11 (6H, d, J = 6.4 Hz), 1.20-1.54 (8H, m), 1.60-1.74 (2H, m), 1.74-1.85 (4H, m), 1.85- 2.04 (2H, m), 2.09-2.20 (2H, m), 2.21-2.30 (2H, m), 2.32-2.42 (1H, m), 2.46-2.63 (3H, m), 2.76-2.85 (1H, m), 3.01-3.17 (2H, m), 3.28 (1H, sep, J = 4.4 Hz), 3.61-3.82 (3H, m), 4.08-4.23 (1H, m), 4.56 (1H, d, J = 7.2 Hz), 4.92 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). Reference Reference 102 example 37 example 117 [00415] [00416] [00417] .sup.1H-NMR (CDCl.sub.3) δ: 1.05 (3H, d, J = 6.0 Hz), 1.06 (3H, d, J = 6.0 Hz), 1.33 (3H, s), 1.36-1.51 (2H, m), 1.59-1.86 (5H, m), 1.92-2.12 (5H, m), 2.69 (2H, d, J = 13.2 Hz), 2.31-2.40 (2H, m), 2.40-2.55 (5H, m), 2.61-2.73 (1H, m), 2.95-3.27 (4H, m), 3.62-3.80 (3H, m), 4.06-4.30 (2H, m), 4.54 (1H, d, J = 9.2 Hz). Reference Reference 103 example 37 example 118 [00418] [00419] [00420] .sup.1H-NMR (CDCl.sub.3) δ: 0.71 (3H, t, J = 7.2 Hz), 1.05 (3H, d, J = 6.0 Hz), 1.06 (3H, d, J = 6.0 Hz), 1.32-1.54 (3H, m), 1.54-1.87 (7H, m), 1.91-2.04 (2H, m), 2.04- 2.21 (2H, m), 2.30 (2H, d, J = 18.0 Hz), 2.33-2.42 (3H, m), 2.47 (1H, dd, J = 16.4, 8.0 Hz), 2.60-2.76 (1H, m), 2.88-3.11 (3H, m), 3.14-3.26 (1H, m), 3.79 (2H, d, J = 13.6 Hz), 4.06-4.29 (2H, m), 4.53 (1H, d, J = 9.2 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 104 example 102 example 115 [00421] [00422] [00423] .sup.1H-NMR (CDCl.sub.3) δ: 0.95 (6H, d, J = 6.1 Hz), 1.29-1.87 (12H, m), 1.33 (3H, s), 1.90-2.04 (1H, m), 2.04-2.31 (8H, m), 2.31-2.43 (1H, m), 2.52-2.67 (2H, m), 3.00- 3.31 (3H, m), 3.35-3.43 (1H, m), 3.63-3.79 (2H, m), 4.12-4.29 (1H, m), 4.49 (1H, d, J = 9.2 Hz), 4.80- 5.02 (1H, m). Reference Reference 105 example 103 example 115 [00424] [00425] [00426] .sup.1H-NMR (CDCl.sub.3) δ: 1.12 (6H, br s), 1.29-1.42 (2H, m), 1.33 (3H, s), 1.42-1.53 (2H, m), 1.54-1.85 (8H, m), 1.90-2.21 (6H, m), 2.21-2.30 (2H, m), 2.32-2.41 (1H, m), 2.59-2.71 (1H, m), 3.03-3.20 (3H, m), 3.25-3.60 (2H, m), 3.61-3.74 (3H, m), 4.17-4.30 (1H, m), 4.56 (1H, d, J = 9.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 106 example 104 example 115 [00427] [00428] [00429] .sup.1H-NMR (CDCl.sub.3) δ: 1.01 (6H, d, J = 5.5 Hz), 1.24-1.84 (8H, m), 1.33 (3H, s), 1.90-2.03 (1H, m), 2.07-2.30 (5H, m), 2.30-2.47 (4H, m), 2.96-3.77 (4H, m), 3.22- 3.30 (1H, m), 3.49-3.57 (1H, m), 3.66-3.75 (2H, m), 4.10-4.24 (1H, m), 4.56 (1H, d, J = 8.5 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 107 example 105 example 115 [00430] [00431] [00432] .sup.1H-NMR (CDCl.sub.3) δ: 0.92 (3H, d, J = 4.3 Hz), 0.94 (3H, d, J = 4.3 Hz), 1.34 (3H, s), 1.36-1.54 (3H, m), 1.58-1.84 (7H, m), 1.91-2.21 (4H, m), 2.22-2.46 (6H, m), 2.46-2.58 (1H, m), 2.97-3.24 (4H, m), 3.65-3.74 (2H, m), 4.15-4.25 (2H, m), 4.58 (1H, d, J = 9.2 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 108 example 106 example 115 [00433] [00434] [00435] .sup.1H-NMR (CDCl.sub.3) δ: 1.10 (6H, br s), 1.34 (3H, s), 1.39- 1.54 (3H, m), 1.54-1.85 (6H, m), 1.91-2.04 (1H, m), 2.04-2.21 (2H, m), 2.21-2.31 (2H, m), 2.32-2.58 (2H, m), 2.62-2.80 (1H, m), 3.05-3.19 (3H, m), 3.24-3.35 (1H, m), 3.29 (3H, s), 3.61-3.79 (3H, m), 3.92-4.01 (1H, m), 4.15-4.30 (1H, m), 4.65 (1H, d, J = 9.2 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 109 example 107 example 115 [00436] [00437] [00438] .sup.1H-NMR (CDCl.sub.3) δ: 0.94-1.29 (8H, m), 1.33 (3H, s), 1.38-1.86 (14H, m), 1.89-2.18 (2H, m), 2.18-2.31 (2H, m), 2.31-2.75 (4H, m), 2.98-3.51 (4H, m), 3.57-3.79 (2H, m), 4.08-4.26 (1H, m), 4.51 (1H, d, J = 8.4 Hz), 4.91 (1H, dddd, J = 63.6, 6.4, 6.4, 4.0 Hz). Reference Reference 110 example 61 example 115 [00439] [00440] [00441] .sup.1H-NMR (CDCl.sub.3) δ: 0.93-1.04 (9H, m), 1.23-1.53 (6H, m), 1.61-1.75 (2H, m), 1.75-1.87 (4H, m), 1.90-2.04 (2H, m), 2.10-2.22 (1H, m), 2.22-2.30 (2H, m), 2.30- 2.41 (2H, m), 2.54 (1H, sep, J = 6.4 Hz), 2.62-2.81 (4H, m), 2.88 (1H, t, J = 11.0 Hz), 3.02-3.12 (1H, m), 3.12-3.22 (1H, m), 3.62-3.72 (1H, m), 3.74-3.84 (1H, m), 4.10-4.24 (1H, m), 4.48 (1H, d, J = 7.4 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 111 example 62 example 115 [00442] [00443] [00444] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-1.00 (6H, m), 1.09 (3H, d, J = 6.0 Hz), 1.33 (3H, s), 1.42-1.54 (3H, m), 1.60-1.89 (5H, m), 1.90-2.22 (3H, m), 2.22-2.42 (4H, m), 2.42- 2.67 (4H, m), 2.68-2.79 (2H, m), 2.83-2.94 (1H, m), 3.03-3.18 (2H, m), 3.64-3.77 (2H, m), 4.10-4.27 (1H, m), 4.53 (1H, d, J = 8.4 Hz), 4.91 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). Reference Reference 112 example 82 example 115 [00445] [00446] [00447] .sup.1H-NMR (CDCl.sub.3) δ: 0.92-1.02 (6H, m), 1.33 (3H, s), 1.35-1.53 (3H, m), 1.54-1.85 (5H, m), 1.86-2.04 (3H, m), 2.08 (3H, s), 2.10-2.20 (1H, m), 2.20-2.28 (2H, m), 2.31-2.42 (1H, m), 2.56-2.68 (2H, m), 2.70-2.80 (3H, m), 2.85-2.97 (1H, m), 3.02-3.16 (3H, m), 3.66- 3.77 (2H, m), 4.05-4.20 (1H, m), 4.59 (1H, d, J = 7.2 Hz), 4.92 (1H, dddd, J = 64.0, 6.0, 6.0, 4.0 Hz). Reference Reference 113 example 83 example 115 [00448] [00449] [00450] .sup.1H-NMR (CDCl.sub.3) δ: 1.02-1.12 (6H, m), 1.30-1.54 (6H, m), 1.58-1.89 (6H, m), 1.89-2.04 (2H, m), 2.09-2.29 (7H, m), 2.29-2.41 (2H, m), 2.42-2.52 (1H, m), 2.52- 2.62 (1H, m), 2.72-2.87 (2H, m), 3.03-3.18 (2H, m), 3.23 (1H, quint, J = 7.6 Hz), 3.63-3.78 (2H, m), 4.07-4.22 (1H, m), 4.55 (1H, d, J = 7.2 Hz), 4.91 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). Reference Reference 114 example 84 example 115 [00451] [00452] [00453] .sup.1H-NMR (CDCl.sub.3) δ: 0.93-1.05 (6H, m), 1.19-1.30 (2H, m), 1.33 (3H, s), 1.37-1.53 (3H, m), 1.60-1.84 (6H, m), 1.85-2.04 (2H, m), 2.05-2.21 (5H, m), 2.21-2.30 (2H, m), 2.30-2.42 (2H, m), 2.46-2.58 (2H, m), 2.61- 2.69 (1H, m), 2.76-2.86 (1H, m), 2.91-3.03 (1H, m), 3.03-3.17 (2H, m), 3.68-3.80 (2H, m), 4.07-4.22 (1H, m), 4.55 (1H, d, J = 7.2 Hz), 4.91 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). Reference Reference 115 example 85 example 115 [00454] [00455] [00456] .sup.1H-NMR (CDCl.sub.3) δ: 0.36-0.43 (2H, m), 0.43-0.50 (2H, m), 1.33 (3H, s), 1.34-1.53 (3H, m), 1.55-1.77 (5H, m), 1.77-1.86 (1H, m), 1.86-2.04 (3H, m), 2.10-2.30 (6H, m), 2.31-2.42 (1H, m), 2.52-2.73 (3H, m), 2.81 (1H, td, J = 8.4, 4.4 Hz), 2.89 (1H, t, J = 7.6 Hz), 2.98-3.17 (3H, m), 3.62-3.77 (2H, m), 4.09-4.23 (1H, m), 4.54 (1H, d, J = 8.0 Hz), 4.91 (1H, dddd, J = 64.0 6.0, 6.0, 4.0 Hz). Reference Reference 116 example 105 example 8 [00457] [00458] [00459] .sup.1H-NMR (CDCl.sub.3) δ: 0.89 (3H, d, J = 6.8 Hz), 0.90 (3H, d, J = 6.8 Hz), 1.17-1.24 (4H, m), 1.30 (3H, s), 1.35-1.49 (2H, m), 1.56-1.85 (6H, m), 1.93-2.28 (8H, m), 2.28-2.37 (1H, m), 2.40-2.49 (1H, m), 2.56-2.68 (1H, m), 2.89-2.99 (1H, m), 3.02-3.24 (3H, m), 3.61- 3.76 (2H, m), 4.08-4.28 (2H, m), 4.55 (1H, d, J = 9.2 Hz). Reference Reference 117 example 95 example 115 [00460] [00461] [00462] .sup.1H-NMR (CDCl.sub.3) δ: 1.05 (6H, d, J = 6.7 Hz), 1.33 (3H, s), 1.43-1.54 (2H, m), 1.57-1.84 (7H, m), 1.88-2.03 (2H, m), 2.10-2.22 (2H, m), 2.22-2.30 (2H, m), 2.31- 2.71 (10H, m), 3.02-3.17 (2H, m), 3.64-3.79 (2H, m), 3.88-4.03 (1H, m), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz), 5.05 (1H, d, J = 7.3 Hz). Reference Reference 118 example 108 example 115 [00463] [00464] [00465] .sup.1H-NMR (CDCl.sub.3) δ: 0.13 (2H, d, J = 4.3 Hz), 0.50 (2H, d, J = 7.3 Hz), 0.84-0.95 (1H, m), 1.33 (3H, s), 1.36-1.54 (3H, m), 1.56-1.87 (7H, m), 1.91-2.21 (4H, m), 2.21-2.30 (2H, m), 2.31-2.46 (3H, m), 2.47-2.60 (1H, m), 2.95-3.27 (4H, m), 3.64-3.74 (2H, m), 4.10- 4.25 (2H, m), 4.56 (1H, d, J = 8.5 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 119 example 109 example 8 [00466] [00467] [00468] .sup.1H-NMR (CDCl.sub.3) δ: 0.86 (9H, s), 1.18-1.24 (4H, m), 1.30 (s, 3H), 1.35-1.50 (2H, m), 1.55-1.72 (3H, m), 1.72-1.86 (2H, m), 1.86-2.00 (1H, m), 2.00-2.29 (7H, m), 2.46 (1H, dd, J = 10.0, 4.0 Hz), 2.53-2.62 (1H, m), 2.62-2.71 (1H, m), 2.98 (1H, dd, J = 10.0, 6.4 Hz), 3.03-3.27 (313, m), 3.61-3.78 (2H, m), 4.03-4.12 (1H, m), 4.13-4.29 (1H, m), 4.53 (1H, d, J = 9.2 Hz). Reference Reference 120 example 109 example 115 [00469] [00470] [00471] .sup.1H-NMR (CDCl.sub.3) δ: 0.87 (9H, s), 1.33 (3H, s), 1.33- 1.54 (3H, m), 1.56-1.85 (6H, m), 1.86-2.31 (7H, m), 2.32-2.42 (1H, m), 2.43-2.52 (1H, m), 2.54-2.75 (2H, m), 2.89-3.26 (413, m), 3.63-3.80 (2H, m), 4.02-4.12 (1H, m), 4.13-4.29 (1H, m), 4.54 (1H, d, J = 9.2 Hz), 4.92 (1H, dddd, J = 63.6, 6.4, 6.4, 4.0 Hz). Reference Reference 121 example 110 example 115 [00472] [00473] [00474] .sup.1H-NMR (CDCl.sub.3) δ: 0.19-0.38 (4H, m), 1.03-1.17 (3H, m), 1.32-1.54 (4H, m), 1.34 (3H, s), 1.56-1.84 (6H, m), 1.90-2.56 (10H, m), 3.01-3.24 (4H, m), 3.63-3.75 (213, m), 4.10-4.27 (2H, m), 4.57 (1H, d, J = 9.2 Hz), 4.92 (1H, dddd, J = 63.5, 6.0, 6.0, 3.7 Hz). Reference Reference 122 example 108 example 8 [00475] [00476] [00477] .sup.1H-NMR (CDCl.sub.3) δ: 0.06-0.16 (2H, m), 0.44-0.52 (2H, m), 0.81-0.93 (1H, m), 1.09-1.23 (5H, m), 1.30 (3H, s), 1.34-1.49 (2H, m), 1.54-1.85 (4H, m), 1.94-2.26 (6H, m), 2.26-2.42 (3H, m), 2.46-2.54 (1H, m), 2.70- 2.79 (1H, m), 3.02-3.26 (4H, m), 3.61-3.74 (2H, m), 4.09-4.27 (2H, m), 4.56 (1H, d, J = 9.2 Hz). Reference Reference 123 example 63 example 115 [00478] [00479] [00480] .sup.1H-NMR (CDCl.sub.3) δ: 0.97-1.09 (6H, m), 1.32 (3H, s), 1.36-1.53 (4H, m), 1.53-1.69 (3H, m), 1.69-1.87 (4H, m), 1.91-2.04 (2H, m), 2.04-2.20 (3H, m), 2.20-2.28 (5H, m), 2.30-2.42 (2H, m), 2.62-2.77 (2H, m), 2.82- 2.95 (2H, m), 3.03-3.15 (2H, m), 3.63- 3.76 (2H, m), 4.03-4.18 (1H, m), 4.52 (1H, d, J = 7.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 124 example 64 example 115 [00481] [00482] [00483] .sup.1H-NMR (CDCl.sub.3) δ: 1.18-1.36 (5H, m), 1.36-1.54 (3H, m), 1.60-2.05 (13H, m), 2.06-2.20 (2H, m), 2.21-2.30 (2H, m), 2.34-2.43 (1H, m), 2.45-2.66 (7H, m), 2.74- 2.83 (1H, m), 3.01-3.16 (2H, m), 3.72-3.82 (1H, m), 3.72-3.82 (1H, m), 4.09-4.23 (1H, m), 4.57 (1H, d, J = 7.2 Hz), 4.92 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). Reference Reference 125 example 65 example 115 [00484] [00485] [00486] .sup.1H-NMR (CDCl.sub.3) δ: 0.97-1.10 (6H, m), 1.21-1.35 (4H, m), 1.35-1.52 (2H, m), 1.62-1.76 (4H, m), 1.76-1.87 (2H, m), 1.87-2.22 (4H, m), 2.22-2.31 (2H, m), 2.31- 2.42 (3H, m), 2.48-2.64 (3H, m), 2.64-2.80 (2H, m), 2.98-3.09 (1H, m), 3.09-3.24 (3H, m), 3.58-3.70 (1H, m), 3.76-3.88 (1H, m), 4.07-4.24 (1H, m), 4.52 (1H, d, J = 8.0 Hz), 4.91 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). Reference Reference 126 example 110 example 8 [00487] [00488] [00489] .sup.1H-NMR (CDCl.sub.3) δ: 0.22-0.34 (4H, m), 1.04-1.24 (8H, m), 1.31 (3H, s), 1.33-1.49 (2H, m), 1.54-1.84 (6H, m), 1.93-2.55 (9H, m), 3.02-3.24 (4H, m), 3.61-3.74 (2H, m), 4.11-4.27 (2H, m), 4.56 (1H, d, J = 9.2 Hz). Reference Reference 127 example 66 example 115 [00490] [00491] [00492] .sup.1H-NMR (CDCl.sub.3) δ: 1.00-1.12 (6H, m), 1.21-1.40 (5H, m), 1.40-1.59 (6H, m), 1.59-1.74 (4H, m), 1.74-1.84 (1H, m), 1.84-2.06 (2H, m), 2.08-2.22 (1H, m), 2.22- 2.43 (8H, m), 2.43-2.65 (5H, m), 3.03-3.12 (1H, m), 3.12-3.22 (1H, m), 3.63-3.73 (1H, m), 3.73-3.83 (1H, m), 4.07-4.23 (1H, m), 4.56 (1H, d, J = 8.0 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 128 example 86 example 115 [00493] [00494] [00495] .sup.1H-NMR (CDCl.sub.3) δ: 0.86 (6H, d, J = 6.8 Hz), 1.29-1.53 (6H, m), 1.53-1.76 (4H, m), 1.76-2.08 (7H, m), 2.08- 2.28 (6H, m), 2.32-2.41 (1H, m), 2.42-2.52 (1H, m), 2.52-2.63 (1H, m), 2.63--2.73 (1H, m), 2.76-2.90 (3H, m), 3.02-3.17 (2H, m), 3.70 (2H, tt, J = 14.8, 4.55 (1H, 4.0 Hz), 4.07-4.22 (1H, m), d, J = 8.0 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz) Reference Reference 129 example 67 example 115 [00496] [00497] [00498] .sup.1H-NMR (CDCl.sub.3) δ: 0.90-1.84 (20H, m), 1.84-2.04 (3H, m), 2.05-2.31 (5H, m), 2.32-2.43 (1H, m), 2.43-2.77 (6H, m), 2.79-2.95 (1H, m), 3.03-3.19 (2H, m), 3.65- 3.81 (2H, m), 4.08-4.24 (1H, m), 4.54 (1H, d, J = 7.9 Hz), 4.93 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Commercial 130 example 110 product [00499] [00500] [00501] .sup.1H-NMR (CDCl.sub.3) δ: 0.16-0.48 (4H, m), 0.98-1.28 (4H, m), 1.25 (3H, s), 1.30-1.50 (2H, m), 1.50-1.89 (7H, m), 1.95-2.21 (5H, m), 2.22-2.65 (2H, m), 2.33 (3H, s), 3.11-3.24 (1H, m), 3.25-3.41 (2H, m), 3.41-3.67 (3H, m), 4.10-4.27 (2H, m), 4.58 (1H, d, J = 7.9 Hz), 7.16 (2H, d, J = 7.9 Hz), 7.21 (2H, d, J = 7.9 Hz). Reference Reference 131 example 68 example 115 [00502] [00503] [00504] .sup.1H-NMR (CDCl.sub.3) δ: 0.88 (3H, s), 0.92-0.98 (6H, m), 1.22-1.52 (8H, m), 1.60-1.84 (6H, m), 1.89-2.03 (2H, m), 2.04 (3H, s), 2.09-2.31 (4H, m), 2.31-2.41 (1H, m), 2.41-2.55 (3H, m), 2.70-2.80 (1H, m), 3.00-3.23 (3H, m), 3.64-3.75 (1H, m), 3.75-3.85 (1H, m), 4.06- 4.22 (1H, m), 4.58 (1H, d, J = 7.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 132 example 94 example 115 [00505] [00506] [00507] .sup.1H-NMR (CDCl.sub.3) δ: 1.04 (6H, d, J = 6.7 Hz), 1.31 (3H, s), 1.41-2.05 (9H, m), 2.14-2.27 (3H, m), 2.31-2.59 (5H, m), 2.64-2.77 (1H, m), 2.85-2.96 (1H, m), 2.99- 3.10 (2H, m), 3.46-3.74 (6H, m), 4.46-4.53 (1H, m), 4.53-4.68 (1H, m), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 133 example 111 example 115 [00508] [00509] [00510] .sup.1H-NMR (CDCl.sub.3) δ: 0.57-0.69 (2H, m), 0.99-1.10 (2H, m), 1.33 (3H, s), 1.35-1.53 (3H, m), 1.58-1.89 (4H, m), 1.91-2.20 (5H, m), 2.20-2.30 (2H, m), 2.32-2.41 (1H, m), 2.41-2.49 (1H, m), 2.51-2.61 (1H, m), 2.75- 2.94 (3H, m), 3.04-3.26 (4H, m), 3.65-3.75 (2H, m), 4.13-4.27 (2H, m), 4.58 (1H, d, J = 9.2 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 134 example 69 example 115 [00511] [00512] [00513] .sup.1H-NMR (CDCl.sub.3) δ: 0.14-0.34 (4H, m), 0.98-1.10 (3H, m), 1.18-1.37 (6H, m), 1.37-1.54 (3H, m), 1.54-1.74 (2H, m), 1.74-1.84 (2H, m), 1.84-2.03 (2H, m), 2.03- 2.42 (12H, m), 2.46-2.57 (2H, m), 2.62-2.72 (1H, m), 2.79-2.90 (1H, m), 3.01-3.20 (2H, m), 3.65-3.74 (1H, m), 3.74-3.85 (1H, m), 4.07-4.21 (1H, m), 4.55 (1H, d, J = 7.3 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 135 example 112 example 115 [00514] [00515] [00516] .sup.1H-NMR (CDCl.sub.3) δ: 0.58-0.72 (2H, m), 0.93-1.02 (2H, m), 1.29-1.54 (4H, m), 1.33 (3H, s), 1.55-1.84 (4H, m), 1.90-2.03 (2H, m), 2.03-2.21 (2H, m), 2.21-2.30 (2H, m), 2.30-2.50 (3H, m), 2.55-2.82 (3H, m), 3.00- 3.24 (4H, m), 3.65-3.75 (2H, m), 4.08-4.27 (2H, m), 4.56 (1H, d, J = 9.2 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 136 example 70 example 115 [00517] [00518] [00519] .sup.1H-NMR (CDCl.sub.3) δ: 0.52-0.66 (2H, m), 0.99-1.09 (2H, m), 1.16-1.36 (3H, m), 1.33 (3H, s), 1.36-1.53 (3H, m), 1.53-1.84 (5H, m), 1.84-2.03 (2H, m), 2.04-2.20 (2H, m), 2.21-2.31 (2H, m), 2.31-2.47 (5H, m), 2.47- 2.60 (2H, m), 2.63-2.92 (4H, m), 3.04-3.19 (2H, m), 3.68-3.79 (2H, m), 4.08-4.23 (1H, m), 4.49-4.62 (1H, m), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 137 example 87 example 115 [00520] [00521] [00522] .sup.1H-NMR (CDCl.sub.3) δ: 0.13-0.33 (2H, m), 0.52-0.74 (2H, m), 0.90-1.14 (1H, m), 1.23-1.38 (5H, m), 1.38-1.55 (2H, m), 1.57-1.69 (2H, m), 1.69-1.87 (2H, m), 1.87- 2.05 (4H, m), 2.10-2.27 (4H, m), 2.32-2.41 (2H, m), 2.41-2.62 (4H, m), 2.62-2.73 (2H, m), 2.90-3.04 (2H, m), 3.04-3.17 (2H, m), 3.52-3.75 (2H, m), 4.06-4.23 (1H, m), 4.51-4.64 (1H, m), 4.92 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). Reference Reference 138 example 87 example 8 [00523] [00524] [00525] .sup.1H-NMR (CDCl.sub.3) δ: 0.05-0.24 (2H, m), 0.44-0.63 (2H, m), 0.80-1.00 (1H, m), 1.13 (4H, d, J = 6.0 Hz), 1.17-1.23 (4H, m), 1.24-1.50 (5H, m), 1.54-1.86 (4H, m), 1.86-1.99 (2H, m), 2.11-2.24 (4H, m), 2.24-2.45 (4H, m), 2.52-2.73 (2H, m), 2.82-2.96 (2H, m), 3.00- 3.16 (2H, m), 3.58-3.72 (2H, m), 4.06-4.22 (1H, m), 4.55 (1H, d, J = 8.0 Hz). Reference Reference 139 example 123 example 8 [00526] [00527] [00528] .sup.1H-NMR (CDCl.sub.3) δ: 1.01 (6H, d, J = 6.4 Hz), 1.16-1.24 (6H, m), 1.30 (3H, s), 1.54-1.70 (3H, m), 1.81-1.88 (2H, m), 2.09-2.31 (5H, m), 2.34-2.53 (6H, m), 2.53- 2.63 (1H, m), 2.67-2.76 (2H, m), 3.04-3.18 (2H, m), 3.62-3.72 (1H, m), 3.72-3.88 (2H, m), 4.19 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz), 4.68 (1H, d, J = 6.1 Hz). Reference Reference 140 example 71 example 115 [00529] [00530] [00531] .sup.1H-NMR (CDCl.sub.3) δ: 0.57-0.64 (2H, m), 0.87-0.93 (2H, m), 1.10-1.53 (9H, m), 1.54-1.73 (4H, m), 1.74-1.84 (1H, m), 1.84-1.91 (1H, m), 1.91-2.11 (2H, m), 2.11- 2.30 (7H, m), 2.31-2.40 (1H, m), 2.45-2.55 (2H, m), 2.55-2.69 (3H, m), 2.80-2.87 (1H, m), 3.02-3.19 (2H, m), 3.65-3.83 (2H, m), 4.06-4.21 (1H, m), 4.53 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz), 4.83-5.00 (1H, m). Reference Reference 141 example 72 example 115 [00532] [00533] [00534] .sup.1H-NMR (CDCl.sub.3) δ: 0.00-0.06 (2H, m), 0.42-0.49 (2H, m), 0.72-0.83 (1H, m), 1.19-1.42 (3H, m), 1.31 (3H, s), 1.42-1.82 (13H, m), 1.89-2.02 (1H, m), 2.05-2.16 (1H, m), 2.16-2.28 (7H, m), 2.30-2.40 (1H, m), 2.51- 2.60 (1H, m), 2.72-2.85 (1H, m), 2.99-3.09 (1H, m), 3.09-3.18 (1H, m), 3.20-3.26 (1H, m), 3.36-3.41 (1H, m), 3.65-3.74 (1H, m), 3.77-3.85 (1H, m), 3.97-4.10 (1H, m), 4.67 (1H, d, J = 7.3 Hz), 4.90 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 142 example 73 example 115 [00535] [00536] [00537] .sup.1H-NMR (CDCl.sub.3) δ: 0.01-0.22 (2H, m), 0.39-0.64 (2H, m), 0.77-0.97 (1H, m), 1.13-1.52 (6H, m), 1.52-1.87 (13H, m), 1.89-2.03 (1H, m), 2.03-2.72 (10H, m), 3.01-3.32 (4H, m), 3.33-3.50 (1H, m), 3.60-3.72 (1H, m), 3.74-3.87 (1H, m), 3.95-4.12 (1H, m), 4.65 (1H, d, J = 7.9 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 143 example 113 example 115 [00538] [00539] [00540] .sup.1H-NMR (CDCl.sub.3) δ: 1.17-1.86 (18H, m), 1.88-2.20 (5H, m), 2.20-2.30 (2H, m), 2.30-2.42 (1H, m), 2.44-3.03 (3H, m), 3.04-3.24 (4H, m), 3.61-3.75 (2H, m), 4.09- 4.28 (2H, m), 4.60 (1H, d, J = 9.2 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 144 example 74 example 115 [00541] [00542] [00543] .sup.1H-NMR (CDCl.sub.3) δ: 0.02-0.10 (2H, m), 0.44-0.52 (2H, m), 0.76-0.87 (1H, m), 1.24-1.52 (10H, m), 1.58-1.87 (5H, m), 1.89-2.01 (2H, m), 2.06-2.16 (1H, m), 2.16- 2.30 (8H, m), 2.30-2.40 (1H, m), 2.46-2.79 (6H, m), 3.03-3.19 (2H, m), 3.65-3.78 (2H, m), 4.02-4.16 (1H, m), 4.61 (1H, d, J = 7.3 Hz), 4.90 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 145 example 75 example 115 [00544] [00545] [00546] .sup.1H-NMR (CDCl.sub.3) δ: 0.05-0.19 (2H, m), 0.47-0.60 (2H, m), 0.83-0.98 (1H, m), 1.21-1.53 (10H, m), 1.53-2.03 (7H, m), 2.07-2.19 (1H, m), 2.19-2.66 (13H, m), 2.68- 2.83 (2H, m), 3.03-3.15 (2H, m), 3.62-3.80 (2H, m), 4.01-4.18 (1H, m), 4.59 (1H, d, J = 7.9 Hz), 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 146 example 120 example 115 [00547] [00548] [00549] .sup.1H-NMR (CDCl.sub.3) δ: 1.03 (6H, d, J = 6.7 Hz), 1.27-1.39 (5H, m), 1.39-1.51 (1H, m), 1.52-1.83 (4H, m), 1.89- 2.13 (3H, m), 2.17-2.28 (2H, m), 2.29-2.58 (7H, m), 2.58-2.69 (1H, m), 2.75-2.99 (7H, m), 2.99-3.09 (1H, m), 3.34-3.46 (2H, m), 4.35-4.49 (1H, m), 4.89 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 147 example 121 example 8 [00550] [00551] [00552] .sup.1H-NMR (CD.sub.3OD) δ: 0.86 (3H, s), 0.90 (3H, s), 1.01 (3H, d, J = 6.8 Hz), 1.02 (3H, d, J = 6.8 Hz), 1.10- 1.33 (6H, m), 1.31 (3H, s), 1.35-1.49 (2H, m), 1.55- 1.72 (3H, m), 1.84-1.93 (1H, m), 2.13-2.28 (3H, m), 2.30-2.59 (8H, m), 2.66-2.75 (2H, m), 3.09-3.18 (2H, m), 3.28-3.35 (1H, m), 3.53 (1H, d, J = 11.6 Hz), 3.67-3.79 (2H, m). Reference Reference 148 example 76 example 115 [00553] [00554] [00555] .sup.1H-NMR (CDCl.sub.3) δ: 1.15-1.30 (6H, m), 1.33 (3H, s), 1.37-1.57 (3H, m), 1.57-1.85 (6H, m), 1.85-2.03 (3H, m), 2.11-2.30 (3H, m), 2.30-2.61 (4H, m), 3.10-3.22 (2H, m), 3.22-3.42 (1H, m), 3.47-3.68 (4H, m), 3.68- 3.77 (1H, m), 3.77-3.84 (1H, m), 4.04-4.25 (1H, m) 4.91 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 149 example 77 example 115 [00556] [00557] [00558] .sup.1H-NMR (CDCl.sub.3) δ: 0.02-0.19 (2H, m), 0.44-0.59 (2H, m), 0.75-0.90 (1H, m), 1.12-1.28 (1H, m), 1.32 (3H, s), 1.40-1.55 (2H, m), 1.55-1.70 (3H, m), 1.70-1.82 (2H, m), 1.84-2.04 (4H, m), 2.08-2.29 (8H, m), 2.98- 3.20 (4H, m), 3.46-3.56 (2H, m), 3.66-3.76 (2H, m), 4.08-4.23 (1H, m), 4.59-4.73 (1H, m) 4.91 (1H, dddd, J = 64.0, 6.0, 6.0, 4.0 Hz). Reference Reference 150 example 114 example 115 [00559] [00560] [00561] .sup.1H-NMR (CDCl.sub.3) δ: 1.32-1.55 (6H, m), 1.35 (3H, s), 1.58-1.86 (6H, m), 1.91-2.11 (3H, m), 2.11-2.21 (1H, m), 2.22-2.31 (2H, m), 2.32-3.05 (6H, m), 3.06-3.24 (3H, m), 3.64-3.76 (2H, m), 4.08-4.28 (2H, m), 4.30- 4.35 (2H, m), 4.44-4.51 (2H, m), 4.60 (1H, d, J = 8.5 Hz), 4.93 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 151 example 122 example 115 [00562] [00563] [00564] .sup.1H-NMR (CDCl.sub.3) δ: 1.07 (6H, d, J = 5.5 Hz), 1.14-1.25 (6H, m), 1.31 (3H, s), 1.31-1.43 (2H, m), 1.43-1.79 (4H, m), 1.83-1.93 (1H, m), 2.13-2.26 (4H, m), 2.26- 2.82 (12H, m), 3.01-3.16 (2H, m), 3.29-3.42 (1H, m), 3.59-3.76 (2H, m), 5.80-6.06 (1H, brs). Reference Reference 152 example 78 example 115 [00565] [00566] [00567] .sup.1H-NMR (CDCl.sub.3) δ: 0.90-1.12 (6H, m), 1.22-1.53 (7H, m), 1.54-2.05 (7H, m), 2.08-2.20 (1H, m), 2.20-2.29 (2H, m), 2.30-2.40 (1H, m), 2.48-3.04 (10H, m), 3.04- 3.17 (2H, m), 3.66-3.80 (2H, m), 4.02-4.17 (1H, m), 4.72 (1H, s), 4.90 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 153 example 125 example 115 [00568] [00569] [00570] .sup.1H-NMR (CDCl.sub.3) δ: 0.89-1.17 (6H, m), 1.33 (3H, s), 1.42-1.69 (6H, m), 1.69-1.89 (2H, m), 1.91-2.04 (1H, m), 2.04-2.14 (1H, m), 2.14-2.82 (8H, m), 2.99-3.13 (2H, m), 3.28-3.77 (6H, m), 4.20-4.35 (1H, m), 4.68- 4.80 (1H, m), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz), 4.94 (1H, d, J = 8.5 Hz). Reference Reference 154 example 88 example 115 [00571] [00572] [00573] .sup.1H-NMR (CDCl.sub.3) δ: 1.03-1.21 (6H, m), 1.35 (3H, s), 1.41-1.90 (8H, m), 1.91-2.61 (11H, m), 2.61-2.71 (1H, m), 2.71-3.04 (4H, m), 3.05-3.21 (2H, m), 3.64-3.79 (2H, m), 4.11-4.27 (1H, m , 4.63 (1H, d, J = 9.8 Hz), 4.93 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). Reference Reference 155 example 126 example 115 [00574] [00575] [00576] .sup.1H-NMR (CDCl.sub.3) δ: 0.93-1.14 (6H, m), 1.33 (3H, s), 1.43-1.54 (1H, m), 1.54-1.81 (5H, m), 1.82-2.32 (11H, m), 2.32-2.45 (2H, m), 2 71-2.85 (1H, m), 2.96-3.24 (6H, m), 3.66-3.82 (2H, m), 4.67-4.80 (1H, m), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz), 4.93 (1H, d, J = 9.2 Hz). Reference Reference 156 example 124 example 115 [00577] [00578] [00579] .sup.1H-NMR (CDCl.sub.3) δ: 0.98-1.38 (10H, m), 1.40-1.78 (10H, m), 1.89-2.11 (3H, m), 2.16-2.32 (2H, m), 2.32-2.42 (1H, m), 2.43-3.44 (9H, m), 3.54-3.77 (2H, m), 4.89- 5.26 (2H, m), 4.93 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz).

[0537] The chemical names of Example 82 to Example 155 are listed below.

Example 82: N-{(1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1R,2R)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 83: N-[(1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)piperidin-4-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 84: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)piperidin-4-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 85: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[5-(propan-2-yl)-1,2,4-oxadiazol-3-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 86: N-{(1R,6S)-2,2-difluoro-6-[5-(propan-2-yl)-1,2,4-oxadiazol-3-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 87: N-[(1R,6S)-2,2-difluoro-6-{[3-(propan-2-yl)-1,2,4-thiadiazol-5-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 88: N-[(1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)-1H-pyrazol-4-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 89: N-[(1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)azetidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 90: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)-1H-pyrazol-4-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 91: N-[(1R,6S)-6-{benzyl[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]amino}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 92: N-[(1R,6S)-2,2-difluoro-6-{[2-(propan-2-yl)pyrimidin-4-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 93: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)-1H-1,2,3-triazol-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 94: N-{(1R,6S)-2,2-difluoro-6-[4-(2-methylpropyl)-1H-1,2,3-triazol-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 95: N-[(1R,6S)-2,2-difluoro-6-{methyl[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]amino}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 96: N-[(1R,6S)-2,2-difluoro-6-{(3S)-3-[methyl(propan-2-yl)amino]pyrrolidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 97: 4-(5-cyclobutyl-1,2,4-oxadiazol-3-yl)-N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 98: N-[(1R,6S)-2,2-difluoro-6-{[(1R,3S,5S)-8-(propan-2-yl)-8-azabicyclo[3.2.1]octan-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 99: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{(3S)-3-[methyl(propan-2-yl)amino]pyrrolidin-1-yl}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 100: N-[(1R,6S)-2,2-difluoro-6-{[(1R,5S,8R)-3-(propan-2-yl)-3-azabicyclo[3.2.1]octan-8-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 101: N-[(1R,6S)-2,2-difluoro-6-{4-[(propan-2-yl)oxy]piperidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 102: 4-(5-cyclobutyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 103: N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-ethyl-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine-1-carboxamide

Example 104: N-[(1R,6S)-2,2-difluoro-6-{[(1R,5S,8S)-3-(propan-2-yl)-3-azabicyclo[3.2.1]octan-8-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 105: N-[(1R,6S)-2,2-difluoro-6-{[(1R,3R,5S)-8-(propan-2-yl)-8-azabicyclo[3.2.1]octan-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 106: N-[(1R,6S)-2,2-difluoro-6-{[(1R,5S,6S)-3-(propan-2-yl)-3-azabicyclo[3.1.0]hexan-6-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 107: N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 108: N-[(1R,6S)-2,2-difluoro-6-{[(3R,4R)-4-methoxy-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 109: N-[(1R,6S)-2,2-difluoro-6-{[4-methyl-1-(propan-2-yl)piperidin-4-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 110: N-{(1R,6S)-2,2-difluoro-6-[(2S)-2-methyl-4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 111: N-{(1R,6S)-2,2-difluoro-6-[(2R)-2-methyl-4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 112: N-[(1R,6S)-2,2-difluoro-6-{(3R)-3-[methyl(propan-2-yl)amino]pyrrolidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 113: N-[(1R,6S)-2,2-difluoro-6-{methyl[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]amino}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 114: N-[(1R,6S)-2,2-difluoro-6-{4-[methyl(propan-2-yl)amino]piperidin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 115: N-[(1R,6S)-6-{(3S)-3-[cyclopropyl(methyl)amino]pyrrolidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 116: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 117: N-[(1R,6R)-2,2-difluoro-6-{[4-(propan-2-yl)piperazin-1-yl]methyl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 118: N-[(1R,6S)-6-{[(3S)-1-(cyclopropylmethyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 119: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-6-{[(3S)-1-(2,2-dimethylpropyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-methylpiperidine-1-carboxamide

Example 120: N-[(1R,6S)-6-{[(3S)-1-(2,2-dimethylpropyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 121: N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-methylcyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 122: N-[(1R,6S)-6-{[(3S)-1-(cyclopropylmethyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexyl]-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carboxamide

Example 123: N-[(1R,6S)-2,2-difluoro-6-{methyl[1-(propan-2-yl)piperidin-4-yl]amino}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 124: N-{(1R,6S)-2,2-difluoro-6-[4-(pyrrolidin-1-yl)piperidin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 125: N-{(1R,6S)-2,2-difluoro-6-[5-(propan-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 126: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-methylcyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-methylpiperidine-1-carboxamide

Example 127: N-{(1R,6S)-2,2-difluoro-6-[2-(propan-2-yl)-2,8-diazaspiro[4.5]decan-8-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 128: N-[(1R,6S)-2,2-difluoro-6-{(3S)-3-[methyl(2-methylpropyl)amino]pyrrolidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 129: N-{(1R,6S)-6-[4-(diethylamino)piperidin-1-yl]-2,2-difluorocyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 130: N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-methylcyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-methyl-4-(4-methylphenyl)piperidine-1-carboxamide

Example 131: N-[(1R,6S)-2,2-difluoro-6-{4-methyl-4-[methyl(propan-2-yl)amino]piperidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 132: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazine-1-carbonyl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 133: N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-fluorocyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 134: N-[(1R,6S)-2,2-difluoro-6-(4-{methyl[(1-methylcyclopropyl)methyl]amino}piperidin-1-yl)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 135: N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-{[1-(trifluoromethyl)cyclopropyl]methyl}pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 136: N-[(1R,6S)-2,2-difluoro-6-(4-{[(1-fluorocyclopropyl)methyl](methyl)amino}piperidin-1-yl)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 137: N-[(1R,6S)-6-{(3S)-3-[(cyclopropylmethyl)(methyl)amino]pyrrolidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 138: N-[(1R,6S)-6-{(3S)-3-[(cyclopropylmethyl)(methyl)amino]pyrrolidin-1-yl}-2,2-difluorocyclohexyl]-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carboxamide

Example 139: rac-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1R,2R,6S)-2-fluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 140: N-{(1R,6S)-2,2-difluoro-6-[4-(methyl{[1-(trifluoromethyl)cyclopropyl]methyl}amino)piperidin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 141: N-[(1R,6S)-6-{(1R,3R,5S)-3-[(cyclopropylmethyl)(methyl)amino]-8-azabicyclo[3.2.1]octan-8-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 142: N-[(1R,6S)-6-{(1R,3S,5S)-3-[(cyclopropylmethyl)(methyl)amino]-8-azabicyclo[3.2.1]octan-8-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 143: N-[(1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-fluoro-2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 144: N-[(1R,6S)-6-{(4S)-4-[(cyclopropylmethyl)(methyl)amino]azepan-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 145: N-[(1R,6S)-6-{(4R)-4-[(cyclopropylmethyl)(methyl)amino]azepan-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 146: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-N,4-dimethylpiperidine-1-carboxamide

Example 147: 4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-N-{(1S,6S)-2,2-dimethyl-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexyl}-4-methylpiperidine-1-carboxamide

Example 148: N-[(1R,6S)-2,2-difluoro-6-{3-[methyl(propan-2-yl)amino]azetidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 149: N-[(1R,6S)-6-{3-[(cyclopropylmethyl)(methyl)amino]azetidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 150: N-[(1R,6S)-2,2-difluoro-6-({(3S)-1-[(3-methyloxetan-3-yl)methyl]pyrrolidin-3-yl}oxy)cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 151: rac-4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methyl-N-{(1S,2S)-2-[4-(propan-2-yl)piperazin-1-yl]cycloheptyl}piperidine-1-carboxamide

Example 152: N-{(1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)-1,4-diazepan-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 153: (1S,2R)-3,3-difluoro-2-[(4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carbonyl)amino]cyclohexyl 4-(propan-2-yl)piperazine-1-carboxylate

Example 154: N-[(1S,6S)-2,2-difluoro-6-{[1-(propan-2-yl)piperidin-4-yl]sulfanyl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 155: N-{(1S,6S)-2,2-difluoro-6-[1-(propan-2-yl)piperidine-4-sulfonyl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

[0538] The compound of the above Reference example 124 which is a diastereomixture and its intermediates for preparing the compound can be obtained as a sole enantiomer by optical resolution with chiral column chromatography or by crystallization with an acid having a chiral center. In addition, the compound of Reference example 124 can be also prepared as a sole enantiomer by using optically-active epoxide as a starting material. Thus, when Reference example 124 as a starting Material A is further determined through separation or asymmetric synthesis, the diastereomixture of Example 156 can be prepared as each diastereomer.

[0539] In addition, the compound of Example 156 which is a diastereomixture can be obtained as a sole enantiomer by optical resolution with chiral column chromatography or by crystallization with an acid having a chiral center. Thus, the two diastereomers of Example 156 can be separated as each diastereomer.

[0540] The compound of Example 156 is a diastereomixture comprising two different diastereomers. These diastereomers can be separated through its process or by optical resolution with chiral column chromatography. It means that the two different diastereomers were substantially prepared.

TABLE-US-00006 Chemical structure of No. diastereomer Chemical name 156-A [00580] 4-{5-[(1S,2S)-2- fluorocyclopropyl]-1,2,4- oxadiazol-3-yl}-N- {(1R,2S,6S)-2-fluoro-6-[4- (propan-2-yl)piperazin-1- yl]cyclohexyl}-4- methylpiperidine-1- carboxamide 156-B [00581] 4-{5-[(1S,2S)-2- fluorocyclopropyl]-1,2,4- oxadiazol-3-yl}-N- {(1S,2R,6R)-2-fluoro-6-[4- (propan-2-yl)piperazin-1- yl]cyclohexyl}-4- methylpiperidine-1- carboxamide

Examples 157-160

[0541] The compounds of Examples 157-160 shown in the table below were prepared according to the process in Example 17 by using the compound of Reference example 80 and each appropriate commercial aldehyde or ketone compound.

TABLE-US-00007 Exam- ple Chemical structure Spectral data 157 [00582] .sup.1H-NMR (CDCl.sub.3) δ: 0.84 (6H, d, J = 6.0 Hz), 1.18-1.35 (4H, m), 1.35-1.54 (3H, m), 1.60-1.84 (8H, m), 1.83-2.04 (2H, m), 2.04-2.31 (11H, m), 2.31-2.41 (1H, m), 2.45-2.56 (1H, m), 2.61-2.71 (1H, m), 2.77-2.87 (1H, m), 3.01-3.20 (2H, m), 3.65-3.75 (1H, m), 3.75-3.86 (1H, m), 4.06-4.22 (1H, m), 4.55 (1H, d, J = 8.0 Hz), 4.91 (1H, ddd, J = 63.6, 6.0, 6.0, 3.6 Hz). 158 [00583] .sup.1H-NMR (CDCl.sub.3) δ: 0.06-0.13 (2H, m), 0.47-0.55 (2H, m), 0.80-0.91 (1H, m), 1.19-1.36 (6H, m), 1.36-1.53 (4H, m), 1.53-1.84 (3H, m), 1.84-2.03 (2H, m) , 2.04-2.21 (2H, m), 2.21-2.45 (10H, m), 2.46-2.58 (2H, m), 2.64-2.71 (1H, m), 2.81-2.89 (1H, m), 3.04-3.19 (2H, m), 3.67-3.79 (2H, m), 4.07-4.22 (1H, m), 4.55 (1H, d, J = 7.9 Hz), 4.92 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz). 159 [00584] .sup.1H-NMR (CDCl.sub.3) δ: 1.15-1.35 (5H, m), 1.35-1.53 (3H, m), 1.53-1.74 (4H, m), 1.74-2.21 (14H, m), 2.21-2.30 (2H, m), 2.30-2.43 (2H, m), 2.44-2.57 (2H, m, 2.61-2.72 (1H, m), 2.74-2.88 (1H, m), 3.00-3.20 (3H, m), 3.65-3.82 (2H, m), 4.05-4.21 (1H, m), 4.54 (1H, d, J = 8.0 Hz), 4.91 (1H, dddd, J = 64.0, 6.0, 6.0, 3.6 Hz). 160 [00585] .sup.1H-NMR (CDCl.sub.3) δ: 1.08-1.83 (16H, m), 1.84-2.03 (3H, m), 2.07-2.43 (9H, m), 2.45-2.76 (5H, m), 2.86-2.98 (1H, m), 3.06-3.20 (2H, m), 3.62-3.77 (2H, m), 4.08-4.23 (1H, m), 4.53 (1H, d, J = 7.9 H), 4.93 (1H, dddd, J = 63.6, 6.0, 6.0, 3.6 Hz).

[0542] The chemical names of Example 157 to Example 160 are listed below.

Example 157: N-[(1R,6S)-2,2-difluoro-6-{4-[methyl(2-methylpropyl)amino]piperidin-1-yl}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 158: N-[(1R,6S)-6-{4-[(cyclopropylmethyl)(methyl)amino]piperidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 159: N-[(1R,6S)-6-{4-[cyclobutyl(methyl)amino]piperidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 160: N-[(1R,6S)-6-{4-[ethyl(methyl)amino]piperidin-1-yl}-2,2-difluorocyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

Example 161

N-[(1R,6S)-2,2-Difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]amino}cyclohexyl]-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

[0543] ##STR00586##

[0544] To a mixture of Reference example 90 (175 mg) and ethanol (1.3 mL) was added palladium carbon (6.4 mg) at room temperature, and the mixture was stirred under hydrogen atmosphere. After the reaction was terminated as judged by LC-MS, the reaction mixture was filtrated with Celite, and concentrated in vacuo. Then, the obtained residue was purified by HPLC (eluate: acetonitrile/water/TFA) to give the title compound (44.1 mg).

[0545] .sup.1H-NMR (CDCl.sub.3) δ: 1.03-1.31 (2H, m), 1.13 (6H, d, J=6.0 Hz), 1.34 (3H, s), 1.38-1.88 (13H, m), 1.91-2.23 (3H, m), 2.27 (2H, d, J=13.2 Hz), 2.33-2.42 (1H, m), 2.42-2.54 (1H, m), 2.95-3.21 (2H, m), 3.32-3.54 (1H, brs), 3.58-3.80 (2H, m), 3.91-4.08 (1H, m), 4.65 (1H, d, J=9.2 Hz), 4.93 (1H, dddd, J=63.6, 6.4, 6.4, 4.0 Hz).

Reference Example 1

rac-(1S,2S)-2-[4-(Propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

[0546] ##STR00587##

Step (i):

[0547] To a mixture of Compound 1 (1.13 g) and dichloromethane (2 mL) was added 1-isopropylpiperazine (1.14 g) at room temperature, and the mixture was stirred for 17 hours. After the reaction was terminated as judged by the consumption of the starting material, diethyl ether was added to the reaction mixture. The precipitate was removed by filtration, and the filtrate was concentrated in vacuo to give a crude product. The obtained crude product was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 2 (1.82 g).

[0548] LCMS: [M+H].sup.+/Rt (min): 256/0.48

Step (ii):

[0549] To a mixture of Compound 2 (1.14 g), acetic acid (2.04 mL), and ethanol (15 mL) was added palladium/carbon (0.95 g) at room temperature, and the mixture was stirred under hydrogen atmosphere for 18 hours. After the reaction was terminated as judged by LC-MS, the reaction mixture was filtrated with Celite, and concentrated in vacuo. Then, the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform) to give the title compound 3 (0.370 g).

[0550] LCMS: [M+H].sup.+/Rt (min): 226/0.31

Reference Example 2

rac-4-(4-Methylphenyl)-N-[(1S,2S)-2-(piperazin-1-yl)cyclohexyl]piperidine-1-carboxamide dihydrochloride

[0551] ##STR00588##

Step (i):

[0552] The title compound 4 (1.28 g) was prepared in the same manner as Step (i) in Reference example 1 by using Compound 1 (1.17 g) and 1-Boc-piperazine (1.72 g).

Step (ii):

[0553] To a solution of Compound 4 (593 mg) in ethanol (9 mL) was added palladium hydroxide (266 mg) at room temperature, and the mixture was stirred under hydrogen atmosphere. After the reaction was terminated as judged by LC-MS, the reaction mixture was filtrated with Celite, and the filtrate was concentrated in vacuo to give the title compound 5 (560 mg).

Step (iii):

[0554] To a mixture of Compound 5 (370 mg), triethylamine (0.91 mL), and dichloromethane (5 mL) was added 4-nitrophenyl chloroformate (316 mg) at 0° C., and the mixture was stirred for 2 hours. Then, 4-(4-methylphenyl)piperidine (297 mg) was added to the reaction mixture at 0° C., and the stirring was continued at room temperature. After the reaction was terminated as judged by the consumption of the reaction intermediate, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 6 (435 mg).

Step (iv):

[0555] To a mixture of Compound 6 (430 mg) and chloroform (3 mL) was added hydrogen chloride/dioxane solution (4 M, 2.22 mL) at 0° C., and the mixture was stirred for 16 hours. Then, the reaction mixture was concentrated in vacuo to give the title compound 7 (310 mg).

[0556] LCMS: [M+H].sup.+/Rt (min): 385/0.71

Reference Example 3

rac-(1R,2S)-2-(4-Ethylpiperazin-1-yl)cyclohexan-1-amine

[0557] ##STR00589##

Step (i):

[0558] To a mixture of Compound 8 (312 mg) and acetic acid (5 mL) was added platinum(IV) oxide (86 mg), and mixture was stirred at 70° C. under hydrogen atmosphere for 6 hour. Then, the reaction mixture was filtrated with Celite, and the filtrate was concentrated in vacuo to give a crude product. The obtained crude product was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 9 (9 mg).

[0559] LCMS: [M+H].sup.+/Rt (min): 212/0.15

Reference Example 4

rac-(1R,2S,6S)-2-Methoxy-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine trihydrochloride

[0560] ##STR00590##

Step (i):

[0561] The title compound 11 (424 mg) was prepared in the same manner as Step (i) in Reference example 3 by using Compound (407 mg).

[0562] LCMS: [M+H].sup.+/Rt (min): 146/0.15

Step (ii):

[0563] To a mixture of Compound 11 (424 mg), triethylamine (1.22 mL), and acetonitrile (10 mL) was added Boc.sub.2O (765 mg) at room temperature, and the mixture was stirred at room temperature. After the reaction was terminated as judged by LC-MS, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 12 (310 mg).

[0564] LCMS: [M+H].sup.+/Rt (min): 246/0.78

Step (iii):

[0565] To a mixture of Compound 12 (141 mg), triethylamine (0.160 mL), and THF (3 mL) was added ethanesulfonyl chloride (0.160 mL) under ice temperature, and the mixture was warmed to room temperature and the stirring was continued. After the reaction was terminated as judged by LC-MS, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 13 (180 mg).

[0566] LCMS: [M+H].sup.+/Rt (min): 338/0.86

Step (iv):

[0567] To a mixture of Compound 13 (155 mg), 1-isopropylpiperazine (236 mg), and 1,4-dioxane (4 mL) was added potassium carbonate (76 mg) at room temperature, and the mixture was stirred for 13 hours heating at 150° C. with a microwave device. Then, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 14 (17 mg).

[0568] LCMS: [M+H].sup.+/Rt (min): 356/0.81

Step (v):

[0569] The title compound 15 (16.8 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 14 (16.3 mg).

[0570] LCMS: [M+H].sup.+/Rt (min): 256/0.32

Reference Example 5

rac-(1S,2S)-2-[4-(Propan-2-yl)piperazin-1-yl]cyclopentane-1-amine

[0571] ##STR00591##

Step (i):

[0572] To a mixture of Compound 16 (315 mg), triethylamine (0.289 mL), and THF (5 mL) was added ethanesulfonyl chloride (0.15 mL), and the mixture was stirred at room temperature for 15 hours. After the reaction was terminated as judged by the consumption of the starting material, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: ethyl acetate/hexane) to give the title compound 17 (140 mg).

[0573] LCMS: [M+H].sup.+/Rt (min): 230/0.44

Step (ii):

[0574] To a mixture of Compound 17 (136 mg) and DMF (4 mL) was added sodium azide (77 mg), and the mixture was stirred at 80° C. for 3.5 hours. After the reaction was terminated as judged by the consumption of the starting material, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo to give the title compound 18 (137 mg).

[0575] LCMS: [M+H].sup.+/Rt (min): 238/0.42

Step (iii):

[0576] To a mixture of Compound 18 (42.4 mg), hydrogen chloride/ethyl acetate solution (4.0 M, 0.711 mL), and ethanol (2.8 mL) was added palladium/carbon (202 mg), and the mixture was stirred under hydrogen atmosphere for 8 hours. After the reaction was terminated as judged by LC-MS, methanol and aqueous sodium bicarbonate were added to the reaction mixture, and the mixture was filtrated with Celite and extracted with chloroform/methanol (6/1). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 19 (98.7 mg).

[0577] LCMS: [M+H].sup.+/Rt (min): 212/0.15

Reference Example 6

rac-(1R,6S)-2,2-Difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-ol

[0578] ##STR00592##

Step (i):

[0579] To a mixture of Compound 20 (688 mg) and ethanol (20 mL) was added 1-isopropylpiperazine (723 mg) at room temperature, and the mixture was stirred for 9 hours heating at 80° C. The reaction mixture was cooled to room temperature, and then concentrated in vacuo. And, the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 21 (830 mg).

[0580] LCMS: [M+H].sup.+/Rt (min): 263/0.35

Reference Example 7

rac-(1R,2S)-3,3-Difluoro-2-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

[0581] ##STR00593##

Step (i):

[0582] To a mixture of DMSO (0.081 mL) and dichloromethane (2 mL) was added oxalyl chloride (0.075 mL) at −78° C., and the mixture was stirred for 20 minutes. Then, a solution of Compound 21 (150 mL) in dichloromethane (2 mL) was added to the reaction mixture, and the mixture was stirred at −78° C. further for 30 minutes. Triethylamine (0.398 mL) was added to the reaction mixture, and the the mixture was warmed to 0° C. Then, the mixture was stirred for 30 minutes, and sodium borohydride was added thereto. The mixture was stirred for 30 minutes. And, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 22 (27 mg).

[0583] LCMS: [M+H].sup.+/Rt (min): 263/0.38

Step (i):

[0584] To a mixture of Compound 22 (27 mg), triethylamine (0.029 mL), and THF (2 mL) was added ethanesulfonyl chloride (0.015 mL), and the mixture was stirred at room temperature. After the reaction was terminated as judged by the consumption of the starting material, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 23 (23 mg).

[0585] LCMS: [M+H].sup.+/Rt (min): 354/0.65

Step (iii):

[0586] The title compound 24 (16.0 mg) was prepared in the same manner as Step (ii) in Reference example 5 by using Compound 23 (23.4 mg).

[0587] LCMS: [M+H].sup.+/Rt (min): 288/0.60

Step (iv):

[0588] To a mixture of Compound 24 (14 mg), THF (1 mL), and water (1 mL) was added triphenylphosphine (25.6 mg) at room temperature, and the mixture was stirred for 4.5 hours heating at 50° C. Then, the reaction mixture was cooled to room temperature, and aqueous hydrochloric acid was added thereto. The mixture was washed with ethyl acetate, and aqueous sodium bicarbonate was added to the aqueous layer. The obtained mixture was extracted with chloroform/methanol (3/1). The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo to give the title compound 25 (7.8 mg).

[0589] LCMS: [M+H].sup.+/Rt (min): 262/0.31

Reference Example 8

4-(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine monohydrochloride

[0590] ##STR00594##

Step (i):

[0591] To a solution of Compound 26 (50.0 g) in ethanol (446 mL) was added 50% aqueous hydroxylamine (132 mL), and the mixture was stirred at 70° C. for 8 hours. The reaction mixture was cooled to room temperature, and water (892 mL) was added to the reaction mixture. The mixture was stirred at room temperature for 30 minutes. The precipitated white crystal was collected on a filter, the obtained crystal was suspended in water (344 mL) again, and the suspension was stirred at room temperature for 30 minutes. The precipitated white solid was collected on a filter and dried to give the title compound 27 (52.3 g).

[0592] LCMS: [M+H].sup.+/Rt (min): 258/0.52 (Method C)

Step (ii):

[0593] To a mixture of Compound 27 (52.3 g), cyclopropanecarboxylic acid (18.4 g), HATU (85 g), and THF (406 mL) in ice bath was added slowly dropwise triethylamine (142 mL), and the mixture was stirred at room temperature for 12 hours. To the reaction mixture was added ethyl acetate (406 mL), and the mixture was washed with water (406 mL) and brine (406 mL). The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 28 (59.1 g).

[0594] LCMS: [M+H].sup.+/Rt (min): 326/0.77 (Method C)

Step (iii):

[0595] A mixture of Compound 28 (59.1 g), DBU (54.2 mL), and toluene (727 mL) was stirred under reflux for one hour. The reaction mixture was cooled to room temperature, and washed with water (727 mL). The organic layer was concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 29 (54.5 g).

[0596] LCMS: [M+H].sup.+/Rt (min): 308/1.11

Step (iv):

[0597] The title compound 30 (35.3 g) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 29 (54.5 g).

[0598] LCMS: [M+H].sup.+/Rt (min): 208/0.30 (Method C)

Reference Examples 9 to 12′

[0599] The compounds of Reference examples 9 to 12′ shown in the table below were prepared according to the process in the above Reference example 8, by using each appropriate starting compound instead of cyclopropanecarboxylic acid at Step (ii) in Reference example 8.

TABLE-US-00008 Instrumental Reference Starting analytical example compound Chemical structure data  9 [00595] [00596] LCMS: [M + H].sup.+/Rt (min): 196/0.32 (Method C) 10 [00597] [00598] LCMS: [M + H].sup.+/Rt (min): 218/0.44 11 [00599] [00600] LCMS: [M + H].sup.+/Rt (min): 226/0.29 (Method C) 12 [00601] [00602] LCMS: [M + H].sup.+/Rt (min): 222/0.46 (Method C) 12′ [00603] [00604] LCMS: [M + H].sup.+/Rt (min): 222/0.46 (Method C)

Reference Example 9: 4-(5-ethyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine monohydrochloride

Reference Example 10: 4-[5-(difluoromethyl)-1,2,4-oxadiazol-3-yl]-4-methylpiperidine monohydrochloride

Reference Example 11: 4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine monohydrochloride

Reference Example 12: 4-methyl-4-{5-[(1R,2S)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine monohydrochloride

Reference Example 12′: 4-methyl-4-{5-[(1S,2R)-2-methylcyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine monohydrochloride

Reference Example 13

[0600] rac-tert-Butyl 4-(6-{[4-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine-1-carbonyl]amino}cyclohex-1-en-1-yl)-3,6-dihydropyridine-1(2H)-carboxylate

##STR00605##

Step (i):

[0601] To a mixture of Compound 35 (192 mg), cerium(III) chloride heptahydrate (309 mg), and methanol (3 mL) was added sodium borohydride (51.4 mg) under ice temperature, and the mixture was stirred at the same temperature for 3 hours. To the reaction mixture was added aqueous sodium bicarbonate, and the mixture was extracted with chloroform/methanol (6/1). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 36 (120 mg).

[0602] LCMS: [M+H].sup.+/Rt (min): 280/0.97

Step (ii):

[0603] To a mixture of Compound 36 (115 mg), triethylamine (0.143 mL), and THF (2 mL) was added ethanesulfonyl chloride (0.058 mL) under ice temperature, and the mixture was stirred for 30 minutes. Then, sodium azide (107 mg) was added to the reaction solution. The mixture was warmed to room temperature, and then the mixture was stirred. After the reaction was terminated as judged by the consumption of the reaction intermediate, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 37 (80 mg).

[0604] LCMS: [M+H].sup.+/Rt (min): 305/1.25

Step (iii)

[0605] The title compound 38 (35 mg) was prepared in the same manner as Step (iv) in Reference example 7 by using Compound (73 mg).

[0606] LCMS: [M+H].sup.+/Rt (min): 279/0.74

Step (iv)

[0607] The title compound 39 (14.0 mg) was prepared in the same manner as Step (iii) in Reference example 2 by using Compound 38 (14.4 mg).

[0608] LCMS: [M+H].sup.+/Rt (min): 512/1.14

Reference Example 14

rac-(1R,6S)-2,2-Difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine trihydrochloride

[0609] ##STR00606##

Step (i):

[0610] The title compound 41 (1.59 g) was prepared in the same manner as Step (ii) in Reference example 4 by using Compound 40 (1.69 g).

[0611] LCMS: [M+H].sup.+/Rt (min): 252/0.73

Step (ii):

[0612] To a mixture of Compound 41 (1.5 g) and THF (30 mL) was added potassium tert-butoxide (1.01 g) under ice temperature, and the mixture was stirred at the same temperature for 20 minutes. Then, tosyl chloride (1.37 g) was added to the reaction mixture under ice temperature, and the reaction mixture was stirred further for 2.5 hours. Water was added to the reaction mixture under ice temperature, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was dissolved in 1,4-dioxane (30 mL), and tosyl chloride (1.37 g) was added to the solution under ice temperature. The solution was heated to 100° C. and stirred for 30 minutes. The reaction solution was cooled to room temperature, and aqueous ammonium chloride was added to the reaction solution. The mixture was extracted with chloroform/ethanol (3/1). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 42 (1.09 g).

[0613] LCMS: [M+H].sup.+/Rt (min): 234/1.01

Step (iii):

[0614] A mixture of Compound 42 (1.09 g), 1-isopropylpiperazine (0.899 g), and ethanol (10 mL) was stirred for 8 hours heating at 120° C. with a microwave device. Then, the reaction solution was concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: ethyl acetate/hexane) to give the title compound 43 (1.32 g).

[0615] LCMS: [M+H].sup.+/Rt (min): 362/0.74

Step (iv):

[0616] The title compound 44 (1.40 g) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound (1.31 g).

[0617] LCMS: [M+H].sup.+/Rt (min): 262/0.19

Reference Examples 15 to 17

[0618] The compounds of Reference examples 15 to 17 shown in the table below were prepared according to the process in the above Reference example 14, by using an optically active isomer of Compound 40 (as Material A) instead of Compound 40 at Step (i) in Reference example 14 and each appropriate starting compound (as Material B) instead of 1-isopropylpiperazine at Step (iii) in Reference example 14.

TABLE-US-00009 Instrumental Reference Material Material Chemical analytical example A B structure data 15 [00607] [00608] [00609] LCMS: [M + H].sup.+/Rt (min): 262/0.19 15′ [00610] [00611] [00612] LCMS: [M + H].sup.+/Rt (min): 262/0.19 (Method C) 16 [00613] [00614] [00615] LCMS: [M + H].sup.+/Rt (min): 274/0.242 17 [00616] [00617] [00618] LCMS: [M + H].sup.+/Rt (min): 288/0.239

Reference Example 15: (1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine trihydrochloride

Reference Example 15′: (1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

Reference Example 16: (1R,6S)-2,2-difluoro-6-[6-(propan-2-yl)-3,6-diazabicyclo[3.1.1]heptan-3-yl]cyclohexan-1-amine

Reference Example 17: (1R,6S)-2,2-difluoro-6-[3-(propan-2-yl)-3,8-diazabicyclo[3.2.1]octan-8-yl]cyclohexan-1-amine

Reference Example 18

(1R,6S)-2,2-Difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

[0619] ##STR00619##

Step (i):

[0620] To a mixture of Compound 48 (5.94 g), sodium bicarbonate (13.2 g), and THF (131 mL) was added 2-nitrobenzenesulfonyl chloride (10.5 g) at room temperature, and the mixture was stirred at the same temperature for 16 hours. To the reaction mixture was added aqueous sodium bicarbonate, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The obtained residue was dissolved in THF (131 mL), and triethylamine (11 mL) and methanesulfonyl chloride (3.67 mL) were added to the solution under ice temperature. The mixture was stirred. After the reaction was terminated as judged by the consumption of the starting material, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was dissolved in acetonitrile (393 mL), and potassium carbonate (16.3 mg) was added to the solution. The mixture was stirred for one hour heating at 80° C. To the reaction mixture was added water, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 49 (9.25 g).

[0621] LCMS: [M+H].sup.+/Rt (min): 319/0.94

Step (ii):

[0622] A mixture of Compound 49 (7.1 g), 1-isopropylpiperazine (3.56 mL), and toluene (22.3 mL) was stirred for one hour heating at 110° C. After the reaction was terminated as judged by the consumption of the starting material, the reaction mixture was concentrated in vacuo, and the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 50 (9.79 g).

[0623] LCMS: [M+H].sup.+/Rt (min): 447/0.68

Step (iii):

[0624] To a mixture of benzenethiol (0.530 mL) and toluene (11.2 mL) was added sodium hydride (55%, 0.215 g) under ice temperature, and the mixture was warmed to room temperature and stirred for 10 minutes. Then, to the reaction mixture was added a solution of Compound 50 (1 g) in toluene (9 mL), and the mixture was stirred heating at 60° C. After the reaction was terminated as judged by the consumption of the starting material, the reaction solution was cooled to 0° C., and 40% aqueous sodium hydroxide was added to the reaction mixture. The mixture was extracted with toluene. To the organic layer was added 5 M hydrochloric acid under ice temperature, and the aqueous layer was extracted from the mixture. To the obtained aqueous layer was added 40% aqueous sodium hydroxide, and the obtained mixture was again extracted with toluene. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 51 (0.47 g).

[0625] LCMS: [M+H].sup.+/Rt (min): 262/0.17

Reference Example 19

2-(4-Methylpiperidin-4-yl)-4,5,6,7-tetrahydro-1,3-benzoxazole

[0626] ##STR00620##

Step (i):

[0627] A mixture of Compound 52 (120 mg), 2-chlorocyclohexanone (68.9 mg), and DMF (1.5 mL) was stirred for 11 hours heating at 130° C. with a microwave device. Then, to the reaction solution was added hydrogen chloride/1,4-dioxane solution (0.25 mL), and the mixture was stirred for hours heating at 130° C. with a microwave device. The reaction solution was concentrated in vacuo, and the obtained residue was dissolved in ethanol. 15% Aqueous sodium hydroxide (2 mL) was added to the solution, and the mixture was stirred for 3 hours heating at 150° C. with a microwave device. To the reaction mixture was added water, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 53 (14 mg).

[0628] LCMS: [M+H].sup.+/Rt (min): 221/0.57

Reference Example 20

4-(5-Cyclopropyl-1,2-oxazol-3-yl)-4-methylpiperidine monohydrochloride

[0629] ##STR00621##

Step (i):

[0630] To a mixture of Compound 54 (900 mg), sodium acetate (650 mg), and methanol (5 mL) was added hydroxylamine hydrochloride (550 mg), and the mixture was stirred at room temperature for 24 hours. The reaction solution was cooled to 0° C., and water was added thereto. The mixture was extracted with chloroform, and the organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound 55 (1.23 g).

Step (ii):

[0631] To a mixture of Compound 55 (416 mg) and DMF (4 mL) was added N-chlorosuccinimide (252 mg), and the mixture was stirred for 3 hours. The reaction solution was cooled to 0° C., and water (6 mL) was added thereto. The precipitated solid was collected on a filter, and dried to give the title compound 56 (326 mg).

Step (iii):

[0632] To a mixture of ethynylcyclopropane (117 mg) and toluene (5 mL) were added Compound 56 (326 mg) and sodium bicarbonate (198 mg), and the mixture was stirred at room temperature. After the reaction was terminated as judged by the consumption of the starting material, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo. Then, the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 57 (348 mg).

[0633] LCMS: [M+H].sup.+/Rt (min): 307/1.13

Step (iv):

[0634] The title compound 58 (307 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 57 (337 mg).

[0635] LCMS: [M+H].sup.+/Rt (min): 207/0.49

Reference Example 21

2-(4-Methylpiperidin-4-yl)-1,3-benzoxazole

[0636] ##STR00622##

Step (i):

[0637] To a solution of Compound 59 (1.46 g) in THF (30 mL) were added isobutyl chloroformate (819 mg) and diisopropylethylamine (3.88 g) under ice temperature, and the mixture was stirred for one hour. 2-Aminophenol (655 mg) was added to the reaction mixture under ice temperature, and the mixture was stirred for 6 hours heating at 70° C. The reaction solution was directly purified by amino silica gel column chromatography (eluate: ethyl acetate/hexane) to give the title compound 60 (710 mg).

[0638] LCMS: [M+H].sup.+/Rt (min): 335/2.28 (Method B)

Step (ii):

[0639] A mixture of Compound 60 (204 mg) and acetic acid (1.10 mL) was stirred for 2 hours heating at 90° C., and concentrated in vacuo. The obtained residue was dissolved in chloroform (2 mL), and trifluoromethanesulfonic acid (2.1 mL) was added to the solution. The mixture was stirred at room temperature for one hour. The reaction solution was concentrated in vacuo, ethyl acetate and aqueous sodium bicarbonate were added to the residue. The mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: ethyl acetate/hexane) to give the title compound 61 (99 mg).

[0640] LCMS: [M+H].sup.+/Rt (min): 217/1.36 (Method B)

Reference Example 22

4-Cyclopentyl-4-methylpiperidine monohydrochloride

[0641] ##STR00623##

Step (i):

[0642] To a mixture of Compound 62 (700 mg) and THF (14 mL) was added lithium diisopropylamide (2 M, 5.18 mL) at −78° C., and the mixture was stirred at the same temperature for 2 hours. To the reaction mixture were added bromocyclopentane (1.23 mL) and potassium iodide (478 mg), and the mixture was warmed to room temperature. The mixture was stirred overnight, and then water was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: ethyl acetate/hexane) to give the title compound 63 (468 mg).

[0643] LCMS: [M+H].sup.+/Rt (min): 312/1.26

Step (ii):

[0644] To a mixture of lithium aluminium hydride (104 mg) and THF (3 mL) were added Compound 63 (371 mg) and THF (6 mL) under ice temperature, and the mixture was stirred for 4 hours. After the reaction was terminated as judged by the consumption of the starting material, water (0.104 mL), 15% aqueous sodium hydroxide (0.104 mL), and then water (0.312 mL) were added to the reaction mixture at 0° C., and the mixture was stirred. The reaction mixture was filtrated. The filtrate was concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: ethyl acetate/hexane) to give the title compound 64 (320 mg).

[0645] LCMS: [M+H].sup.+/Rt (min): 284/1.06

Step (iii):

[0646] To a mixture of Compound 64 (314 mg), triethylamine (0.309 mL), and THF (5 mL) was added methanesulfonyl chloride (0.104 mL), and the mixture was stirred at room temperature. After the reaction was terminated as judged by the consumption of the starting material, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: ethyl acetate/hexane) to give the title compound 65 (290 mg).

[0647] LCMS: [M+H].sup.+/Rt (min): 362/1.15

Step (iv):

[0648] To a mixture of Compound 65 (278 mg) and THF (3 mL) was added lithium triethylborohydride (0.99 M, 1.55 mL), and the mixture was stirred at room temperature. Then, the reaction solution was heated to 70° C. After the reaction was terminated as judged by the consumption of the starting material, the reaction solution was cooled to 0° C., and aqueous ammonium chloride was added to the reaction solution. The mixture was extracted with chloroform, and the organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. Then, the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 66 (100 mg).

[0649] LCMS: [M+H].sup.+/Rt (min): 268/1.42

Step (v):

[0650] The title compound 67 (58.5 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 66 (90 mg).

[0651] LCMS: [M+H].sup.+/Rt (min): 168/0.62

Reference Example 23

4-(4,4-Difluorocyclohexyl)-4-methylpiperidine monohydrochloride

[0652] The compound of Reference example 23 shown in the table below was prepared according to the process in the above Reference example 22, by using 1,1-difluoro-4-iodocyclohexane instead of bromocyclopentane at Step (i) in Reference example 22.

TABLE-US-00010 Instrumental Reference analytical example Chemical structure data 23 [00624] LCMS: [M + H].sup.+/Rt (min): 218/0.57

Reference Example 24

4-(5-Cyclopropyl-1,3,4-thiadiazol-2-yl)-4-methylpiperidine monohydrochloride

[0653] ##STR00625##

Step (i):

[0654] To a mixture of Compound 59 (399 mg), cyclopropanecarbohydrazide hydrochloride (269 mg), and DMF (5 mL) were added HATU (686 mg) and diisopropylethylamine (1.15 mL), and the mixture was stirred at room temperature for 3 hours. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 69 (520 mg).

[0655] LCMS: [M+H].sup.+/Rt (min): 326/0.74

Step (ii):

[0656] To a mixture of Compound 69 (255 mg) and toluene (6 mL) was added Lawesson's reagent (349 mg), and the mixture was stirred under reflux for one hour. The reaction solution was cooled to 0° C., and aqueous sodium bicarbonate was added to the reaction solution. The mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) and then by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 70 (102 mg). LCMS: [M+H].sup.+/Rt (min): 324/1.08

Step (iii):

[0657] The title compound 71 (78 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound (92 mg).

[0658] LCMS: [M+H].sup.+/Rt (min): 224/0.45

Reference Example 25

4-(5-Cyclopropyl-1,3-thiazol-2-yl)-4-methylpiperidine monohydrochloride

[0659] ##STR00626##

Step (i):

[0660] The title compound 72 (796 mg) was prepared in the same manner as Step (i) in Reference example 24 by using Compound (718 mg) and 2-amino-1-cyclopropylethan-1-one hydrochloride (400 mg).

[0661] LCMS: [M+H].sup.+/Rt (min): 325/0.83

Step (ii):

[0662] To a mixture of Compound 72 (127 mg), pyridine (0.063 mL), and toluene (3 mL) was added Lawesson's reagent (205 mg), and the mixture was stirred under reflux for 14 hours. The reaction solution was cooled to room temperature, and then aqueous sodium bicarbonate was added to the reaction solution. The mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 73 (76.3 mg).

[0663] LCMS: [M+H].sup.+/Rt (min): 323/1.43

Step (iii):

[0664] The title compound 74 (66.5 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 73 (77 mg).

[0665] LCMS: [M+H].sup.+/Rt (min): 223/0.67

Reference Example 26

4-(2-Cyclopropyl-1,3-thiazol-4-yl)-4-methylpiperidine monohydrochloride

[0666] ##STR00627##

Step (i):

[0667] A solution of Compound 75 (532 mg) and cyclopropanecarbothioamide (168 mg) in methanol (6 mL) was stirred under reflux for 2.5 hours. The reaction mixture was allowed to cool to room temperature, and then saturated aqueous sodium bicarbonate was added to the reaction mixture. The mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 76 (119 mg).

Step (ii):

[0668] The title compound 77 (137 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 76 (119 mg).

[0669] LCMS: [M+H].sup.+/Rt (min): 223/0.572

Reference Example 27

4-(1-Cyclopropyl-1H-1,2,4-triazol-3-yl)-4-methylpiperidine dihydrochloride

[0670] ##STR00628##

Step (i):

[0671] The title compound 78 (648 mg) was prepared in the same manner as Step (i) in Reference example 24 by using Compound 59 (611 mg) and cyclopropylhydrazine hydrochloride (300 mg). LCMS: [M+H].sup.+/Rt (min): 298/0.80

Step (ii):

[0672] A mixture of Compound 78 (374 mg), ammonium formate (1.43 g), and trimethyl orthoformate (2.78 mL) was stirred heating at 100° C. After the reaction was completed, the reaction solution was concentrated. To the obtained residue was added water, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 79 (163 mg).

[0673] LCMS: [M+H].sup.+/Rt (min): 307/0.89

Step (iii):

[0674] The title compound 80 (142 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 79 (144 mg).

[0675] LCMS: [M+H].sup.+/Rt (min): 207/0.39

Reference Example 28

4-(5-Cyclopropyl-1,2,4-thiadiazol-3-yl)-4-methylpiperidine

[0676] ##STR00629##

Step (i):

[0677] To a solution of Compound 27 (1.04 g) in THF (15 mL) was added thiocarbonylimidazole (0.864 mg) under ice temperature, and the mixture was stirred at room temperature. After the reaction was terminated as judged by the consumption of the starting material, the reaction solution was cooled to 0° C., and water was added to the reaction solution. The mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated in vacuo.

[0678] The obtained residue was dissolved in THF (15 mL), and boron trifluoride-diethyl ether complex (1.52 mL) was added to the solution at 0° C. The mixture was warmed to room temperature under stirring. After the reaction was completed, aqueous sodium bicarbonate was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate).

[0679] To a solution of the purified compound in THF (15 mL) was added hydrogen chloride/dioxane solution (4 M, 5.05 mL) at 0° C., and the mixture was warmed to room temperature and stirred. After the reaction was completed, the reaction solution was concentrated in vacuo, and the obtained residue was dissolved in THF (15 mL). To the solution were added triethylamine (3.38 ml) and 2-nitrobenzenesulfonyl chloride (0.985 g), and the mixture was stirred at room temperature. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 81 (627 mg).

[0680] LCMS: [M+H].sup.+/Rt (min): 385/0.93

Step (ii):

[0681] To a mixture of Compound 81 (590 mg), pyridine (0.248 mL), and toluene (7 mL) was added phosphoryl chloride (0.572 mL), and the mixture was stirred under reflux. After the reaction was completed, the reaction solution was added to aqueous sodium bicarbonate at 0° C., and the mixture was filtrated. The filtrate was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 82 (432 mg).

[0682] LCMS: [M+H].sup.+/Rt (min): 403/1.21

Step (iii):

[0683] To a mixture of Compound 82 (210 mg), cyclopropylzinc(II) bromide (0.5 M, 3.13 mL), and THF (2 mL) was added tetrakis(triphenylphosphine)palladium(0) (30.1 mg), and the mixture was stirred at 60° C. for 1.5 hours. After the reaction was completed, aqueous sodium bicarbonate was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 83 (84 mg).

[0684] LCMS: [M+H].sup.+/Rt (min): 409/1.24

Step (iv):

[0685] To a mixture of Compound 83 (71.4 mg), 1-dodecanethiol (0.251 mL), and acetonitrile (3 mL) was added potassium carbonate (145 mg), and the mixture was stirred at 80° C. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with chloroform/methanol (6/1). The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate=>chloroform/methanol) to give the title compound 84 (38 mg). LCMS: [M+H].sup.+/Rt (min): 224/0.52

Reference Example 29

4-(5-Methoxy-1,2,4-thiadiazol-3-yl)-4-methylpiperidine

[0686] ##STR00630##

Step (i):

[0687] To a solution of Compound 82 (119 mg) in methanol (2 mL) was added sodium methoxide (28%, 285 mg), and the mixture was stirred at room temperature. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was concentrated in vacuo to give the title compound 85 (97.1 mg).

[0688] LCMS: [M+H].sup.+/Rt (min): 399/1.18

Step (ii):

[0689] The title compound 86 (14.9 mg) was prepared in the same manner as Step (iv) in Reference example 28 by using Compound 85 (91.6 mg).

[0690] LCMS: [M+H].sup.+/Rt (min): 214/0.48

Reference Example 30

4-[5-(Cyclopropyloxy)-1,2,4-thiadiazol-3-yl]-4-methylpiperidine

[0691] The compound of Reference example 30 shown in the table below was prepared according to the process in the above Reference example 29, by using cyclopropyl alcohol and sodium hydride instead of sodium methoxide at Step (i) in Reference example 29.

TABLE-US-00011 Instrumental Reference analytical example Chemical structure data 30 [00631] LCMS: [M + H].sup.+/Rt (min): 240/0.56

Reference Example 31

2-[(4-Methylpiperidin-4-yl)oxy]pyridine monohydrochloride

[0692] ##STR00632##

Step (i):

[0693] To a solution of Compound 88 (183 mg) in DMF (2 mL) was added sodium hydride (55%, 48.2 mg) under ice temperature, and the mixture was stirred for 20 minutes. To the reaction mixture was added 2-fluoropyridine (0.109 mL), and the mixture was stirred at room temperature. After the reaction was completed, the reaction mixture was cooled to 0° C. To the reaction mixture was added water, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 89 (18 mg).

[0694] LCMS: [M+H].sup.+/Rt (min): 293/1.29

Step (ii):

[0695] The title compound 90 (13.2 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 89 (14.7 mg).

[0696] LCMS: [M+H].sup.+/Rt (min): 193/0.48

Reference Example 32

4-(2-Fluoro-4-methylphenyl)-4-methylpiperidine

[0697] ##STR00633##

Step (i):

[0698] To a mixture of Compound 91 (211 mg), 1-methyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester (274 mg), potassium carbonate (386 mg), 1,2-dimethoxymethane (4 mL), and water (1 mL) was added dichloro(1,1′-bis(diphenylphosphino)ferrocene)palladium (45.6 mg) at room temperature, and then the mixture was heated under reflux. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 92 (32 mg). LCMS: [M+H].sup.+/Rt (min): 206/0.51

Step (ii):

[0699] To a solution of Compound 92 (137 mg) in THF (3 mL) was added n-butyllithium solution (1.57 M, 0.68 mL) at −18° C., and the mixture was further cooled to −50° C. Dimethyl sulfate was added dropwise to the reaction solution, and the mixture was stirred at −50° C. for one hour. To the reaction solution was added aqueous ammonia, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, and concentrated in vacuo to give a residue.

[0700] The obtained residue was dissolved in methanol (3 mL), and sodium borohydride (80 mg) was added to the solution under ice temperature. After the reaction was completed, aqueous sodium bicarbonate was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 93 (32 mg).

[0701] LCMS: [M+H].sup.+/Rt (min): 222/0.63

Step (iii):

[0702] To a solution of Compound 93 (30.4 mg) in 1,2-dichloroethane (3 mL) was added 1-chloroethyl chloroformate (0.045 mL) at room temperature, and the mixture was heated under reflux. The reaction solution was concentrated in vacuo, and chloroform and aqueous sodium hydroxide were added to the obtained residue. The mixture was stirred at room temperature, and then extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 94 (22 mg). LCMS: [M+H].sup.+/Rt (min): 208/0.66

Reference Example 33

4-[4-(Difluoromethyl)phenyl]-4-methylpiperidine monohydrochloride

[0703] ##STR00634##

Step (i):

[0704] To a solution of Compound 95 (490 mg) in THF (6 mL) was added n-butyllithium solution (1.57 M, 1.15 mL) at −78° C., and the mixture was stirred for 30 minutes. To the reaction solution was added DMF (0.535 mL), and the mixture was warmed to 0° C. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 96 (256 mg).

[0705] LCMS: [M+H]′/Rt (min): 304/1.10

Step (ii):

[0706] To a solution of Compound 96 (157 mg) in dichloromethane (2 mL) was added Deoxo-Fluor® (0.285 mL) under ice temperature, and then the mixture was stirred at room temperature. After the reaction was completed, the reaction solution was added to aqueous sodium bicarbonate in ice bath, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 97 (110 mg).

[0707] LCMS: [M+H].sup.+/Rt (min): 326/1.20

Step (iii):

[0708] The title compound 98 (84.5 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 97 (104.8 mg).

[0709] LCMS: [M+H].sup.+/Rt (min): 226/0.60

Reference Example 34

5-Methyl-2-(4-methylpiperidin-4-yl)benzonitrile

[0710] ##STR00635##

Step (i):

[0711] To a mixture of Compound 99 (267 mg) and m-cresol (1.20 mL) was added trifluoromethanesulfonic acid (1.01 mL), and the mixture was stirred at room temperature. After the reaction was completed, the reaction solution was added to aqueous sodium bicarbonate at 0° C., and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 100 (388 mg).

[0712] LCMS: [M+H].sup.+/Rt (min): 278/1.01

Step (ii):

[0713] To a mixture of Compound 100 (113 mg), potassium carbonate (169 mg), and THF (4 mL) was added N-phenylbis(trifluoromethanesulfonimide) (175 mg), and the mixture was stirred heating at 120° C. with a microwave device. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 101 (138 mg).

[0714] LCMS: [M+H].sup.+/Rt (min): 410/1.26

Step (iii):

[0715] The title compound 102 (40.8 mg) was prepared in the same manner as Step (iii) in Reference example 28 by using Compound 101 (130 mg) and zinc cyanide (55.8 mg).

[0716] LCMS: [M+H].sup.+/Rt (min): 287/1.07

Step (iv):

[0717] To a solution of Compound 102 (40 mg) in 2-propanol (3 ml) was added potassium hydroxide (78 mg) at room temperature, and then the mixture was stirred heating at 110° C. with a microwave device. After the reaction was completed, water was added to the reaction solution. The mixture was extracted with chloroform/ethanol (4/1). The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 103 (20.6 mg).

[0718] LCMS: [M+H].sup.+/Rt (min): 215/0.57

Reference Example 35

(3S,4S)-4-Fluoro-1-(propan-2-yl)pyrrolidin-3-ol

[0719] ##STR00636##

Step (i):

[0720] To a solution of Compound 104 (500 mg) in chloroform (2 mL) was added hydrogen chloride/1,4-dioxane (4 M, 6 mL) at 0° C., and the mixture was warmed to room temperature and stirred. After the reaction was terminated as judged by the consumption of the starting material, the reaction solution was concentrated in vacuo. The obtained residue was dissolved in chloroform (2 mL). To the solution were added acetone (1.79 mL), sodium acetate (200 mg), and sodium triacetoxyborohydride (1.03 g) at 0° C., and the mixture was warmed to room temperature and stirred. After the reaction was completed, aqueous sodium bicarbonate was added to the reaction mixture at 0° C., and the mixture was extracted with chloroform/methanol (5/1). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 105 (348 mg).

[0721] LCMS: [M+H].sup.+/Rt (min): 148/0.17

Reference Example 36

(3R)-4,4-Difluoro-1-(propan-2-yl)pyrrolidin-3-ol

[0722] The compound of Reference example 36 shown in the table below was prepared according to the process in the above

Reference Example 35, by using the appropriate starting compound instead of Compound 104 at Step (i) in Reference example 35

[0723]

TABLE-US-00012 Instrumental Reference analytical example Chemical structure data 36 [00637] LCMS: [M + H].sup.+/Rt (min): 166/0.19

Reference Example 37

(1R,6S)-2,2-Difluoro-6-{[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexan-1-amine

[0724] ##STR00638##

Step (i):

[0725] A mixture of Compound 49 (1.5 g), (S)-1-isopropylpyrrolidin-3-ol (0.792 mg), and NMP (1 mL) was stirred heating at 150° C. After the reaction was terminated as judged by the consumption of the starting material, the reaction solution was directly purified by silica gel column chromatography (eluate: chloroform/methanol/triethylamine) and then by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 106 (1.03 g).

[0726] LCMS: [M+H].sup.+/Rt (min): 448/0.78

Step (ii):

[0727] The title compound 107 (43 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 106 (100 mg).

[0728] LCMS: [M+H].sup.+/Rt (min): 263/0.22

Reference Examples 38 to 40

[0729] The compounds of Reference examples 38 to 40 shown in the table below were prepared according to the process in the above Reference example 37, by using each appropriate starting compound instead of (S)-1-isopropylpyrrolidin-3-ol at Step (i) in Reference example 37.

TABLE-US-00013 Instrumental Reference analytical example Chemical structure data 38 [00639] LCMS: [M + H].sup.+/Rt (min): 263/0.151 39 [00640] LCMS: [M + H].sup.+/Rt (min): 281/0.18 40 [00641] LCMS: [M + H].sup.+/Rt (min): 299/0.35

Reference Example 38: (1R,6S)-2,2-difluoro-6-{[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexan-1-amine

Reference Example 39: (1R,6S)-2,2-difluoro-6-{[(3S,4S)-4-fluoro-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexan-1-amine

Reference Example 40: (1R,6S)-6-{[(3R)-4,4-difluoro-1-(propan-2-yl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexan-1-amine

Reference Example 41

3-Fluoro-5-methyl-2-(piperidin-4-yl)pyridine

[0730] ##STR00642##

Step (i):

[0731] The title compound 109 (90.5 mg) was prepared in the same manner as Step (i) in Reference example 32 by using Compound 108 (72.4 mg) and 1-carbobenzoxy-1,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaboran-2-yl)pyridine.

[0732] LCMS: [M+H].sup.+/Rt (min): 327/1.04 (Method C)

Step (ii):

[0733] To a solution of Compound 109 (88.0 mg) in ethyl acetate (1.5 mL) was added palladium/carbon (88.0 mg), and the mixture was stirred under hydrogen atmosphere for 8 hours. The reaction solution was filtrated with Celite, and the filtrate was concentrated in vacuo to give the title compound 110 (22.2 mg).

[0734] LCMS: [M+H].sup.+/Rt (min): 195/0.35 (Method C)

Reference Example 42

(1R,6S)-2,2-Difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-ol

[0735] ##STR00643##

Step (i):

[0736] To a solution of Compound 111 (300 mg) and sodium bicarbonate (634 mg) in ethanol (10 mL) was added N-benzyl-N,N-bis(2-chloroethyl)amine hydrochloride (586 mg), and the mixture was stirred heating at 120° C. with a microwave device. After the reaction was completed, water was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 112 (398 mg).

[0737] LCMS: [M+H].sup.+/Rt (min): 311/0.46

Step (ii):

[0738] The title compound 113 (289 mg) was prepared in the same manner as Step (ii) in Reference example 2 by using Compound 112 (389 mg).

[0739] LCMS: [M+H].sup.+/Rt (min): 221/0.16

Step (iii):

[0740] To a mixture of Compound 113 (389 mg), acetone (1.73 mL), and dichloromethane (6 mL) was added sodium triacetoxyborohydride (1.5 g) at 0° C., and the mixture was warmed to room temperature and the stirring was continued for 1.5 hours. To the reaction mixture was added water at 0° C., and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 114 (255 mg).

[0741] LCMS: [M+H].sup.+/Rt (min): 263/0.36

Reference Example 43

tert-Butyl [(1S,4R)-3-{[4-(propan-2-yl)piperazin-1-yl]methyl}bicyclo[2.2.1]heptan-2-yl]carbamate

[0742] ##STR00644##

Step (i):

[0743] To a mixture of Compound 115 (239 mg), 1-isopropylaziridine (128 mg), acetic acid (0.086 mL), and THF (2.5 mL) was added sodium triacetoxyborohydride (635 mg) at room temperature, and the mixture was stirred at the same temperature for 3 hours. To the reaction mixture was added aqueous sodium bicarbonate at 0° C., and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 116 (310 mg).

[0744] LCMS: [M+H].sup.+/Rt (min): 352/1.35 (Method B)

Reference Example 44

rac-2-[6-(Propan-2-yl)pyridin-3-yl]cyclohex-2-en-1-amine

[0745] ##STR00645##

Step (i):

[0746] To a mixture of Compound 117 (350 mg), 6-isopropylpyridin-3-yl boronate (273 mg), cesium carbonate (1.28 g), 1,4-dioxane (5 mL), and water (1 mL) was added [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloride dichloromethane adduct (129 mg) at room temperature, and the mixture was stirred at 90° C. for 3 hours. To the reaction mixture was added water at 0° C., and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 118 (168 mg).

Step (ii) to Step (iv):

[0747] The title compound 121 (29.7 mg) was prepared in the same manner as Steps (i) to (iii) in Reference example 13 by using Compound 118 (68.2 mg).

[0748] LCMS: [M+H].sup.+/Rt (min): 217/0.39

Reference Example 45

N-Methyl-N-[(1-methylcyclopropyl)methyl]piperidin-4-amine

[0749] ##STR00646##

Step (i):

[0750] To a solution of Cert-butyl 4-(methylamino)piperidine-1-carboxylate (584 mg), 1-methylcyclopropane-1-carboxylic acid (300 mg), and triethylamine (0.76 mL) in DMF (4 mL) was added HATU (1.24 g), and the mixture was stirred at room temperature. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 123 (926 mg).

Step (ii):

[0751] To a solution of Compound 123 (806 mg) in chloroform (4.5 mL) was added hydrochloric acid (in CPME, 5 M, 2.7 mL) at 0° C., and the reaction solution was warmed to room temperature and stirred. After the reaction was completed, the reaction mixture was concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 124 (477 mg).

Step (iii):

[0752] The title compound 125 (203 mg) was prepared in the same manner as Step (ii) in Reference example 22 by using Compound 124 (413 mg).

[0753] LCMS: [M+H].sup.+/Rt (min):183/0.15

Reference Examples 46-47

[0754] The compounds of Reference examples 46-47 shown in the table below was prepared according to the process in the above Reference example 45, by using each appropriate starting compound instead of 1-methylcyclopropane-1-carboxylic acid at Step (i) in Reference example 45.

TABLE-US-00014 Instrumental Reference analytical example Chemical structure data 46 [00647] LCMS: [M + H].sup.+/Rt (min): 187/0.14 47 [00648] LCMS: [M + H]+/Rt (min): 237/0.19

Reference Example 46: N-[(1-fluorocyclopropyl)methyl]-N-methylpiperidin-4-amine

Reference Example 47: N-methyl-N-{[1-(trifluoromethyl)cyclopropyl]methyl}piperidin-4-amine

Reference Example 48: (3S)-1-{[1-(trifluoromethyl)cyclopropyl]methyl}pyrrolidin-3-ol

[0755] ##STR00649##

Step (i):

[0756] The title compound 127 (196 mg) was prepared in the same manner as Step (i) in Reference example 45 by using (S)-3-pyrrolidinol (103 mg) and 1-(trifluoromethyl)cyclopropane-1-carboxylic acid (200 mg).

Step (ii):

[0757] The title compound 128 (87.2 mg) was prepared in the same manner as Step (iii) in Reference example 45 by using Compound 127 (184 mg).

[0758] LCMS: [M+H].sup.+/Rt (min):210/0.30

Reference Example 49

(1R,3S,5S)—N-(Cyclopropylmethyl)-N-methyl-8-azabicyclo[3.2.1]oxtan-3-amine

[0759] ##STR00650##

Step (i):

[0760] The title compound 130 (178 mg) was prepared in the same manner as Step (iii) in Reference example 42 by using Compound 129 (146 mg) and cyclopropane-carbaldehyde (170 mg).

Step (ii):

[0761] The title compound 131 (106 mg) was prepared in the same manner as Step (ii) in Reference example 45 by using Compound 130 (166 mg).

[0762] LCMS: [M+H].sup.+/Rt (min): 195/0.14

Reference Examples 50-52

[0763] The compounds of Reference examples 50-52 shown in the table below were prepared according to the process in the above Reference example 49, by using each appropriate starting compound instead of Compound 129 at Step (i) in Reference example 49.

TABLE-US-00015 Instrumental Reference analytical example Chemical structure data 50 [00651] LCMS: [M + H].sup.+/Rt (min): 195/0.14 51 [00652] LCMS: [M + H].sup.+/Rt (min): 183/0.14 52 [00653] LCMS: [M + H].sup.+/Rt (min): 183/0.14

Reference Example 50: (1R,3R,5S)—N-(cyclopropylmethyl)-N-methyl-8-azabicyclo[3.2.1]octan-3-amine

Reference Example 51: (4S)—N-(cyclopropylmethyl)-N-methylazepan-4-amine

Reference Example 52: (4R)—N-(cyclopropylmethyl)-N-methylazepan-4-amine

Reference Example 53

(1R,3S,5S)-8-(Propan-2-yl)-8-azabicyclo[3.2.1]octan-3-ol

[0764] ##STR00654##

Step (i):

[0765] The title compound was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 132 (3 g).

Step (ii):

[0766] The title compound 134 (1.98 g) was prepared in the same manner as Step (iii) in Reference example 42 by using Compound 133 and acetone (1.3 g).

[0767] LCMS: [M+H].sup.+/Rt (min): 170/0.15

Reference Examples 54-57

[0768] The compounds of Reference examples 54-57 shown in the table below were prepared according to the process in the above Reference example 53, by using each appropriate starting compound instead of Compound 132 at Step (i) in Reference example 53.

TABLE-US-00016 Instrumental Reference analytical example Chemical structure data 54 [00655] LCMS: [M + H].sup.+/Rt (min): 170/0.25 55 [00656] LCMS: [M + H].sup.+/Rt (min): 170/0.15 56 [00657] LCMS: [M + H].sup.+/Rt (min): 170/0.24 57 [00658] LCMS: [M + H].sup.+/Rt (min): 142/0.15

Reference Example 54: (1R,5S,8R)-3-(propan-2-yl)-3-azabicyclo[3.2.1]octan-8-ol

Reference Example 55: (1R,5S,8S)-3-(propan-2-yl)-3-azabicyclo[3.2.1]octan-8-ol

Reference Example 56: (1R,3R,5S)-8-(propan-2-yl)-8-azabicyclo[3.2.1]octan-3-ol

Reference Example 57: (1R,5S,6S)-3-(propan-2-yl)-3-azabicyclo[3.1.0]hexan-6-ol

Reference Examples 58-79

[0769] The compounds of Reference examples 58-79 shown in the table below were prepared according to the process in the above Reference example 18, by using each appropriate starting compound instead of 1-isopropylpiperazine at Step (ii) in Reference example 18.

TABLE-US-00017 Instrumental Reference analytical example Chemical structure data 58 [00659] LCMS: [M + H].sup.+/Rt (min): 262/0.17 59 [00660] LCMS: [M + H].sup.+/Rt (min): 276/0.28 60 [00661] LCMS: [M + H].sup.+/Rt (min): 277/0.55 61 [00662] LCMS: [M + H].sup.+/Rt (min): 276/0.20 62 [00663] LCMS: [M + H].sup.+/Rt (min): 276/0.20 63 [00664] LCMS: [M + H].sup.+/Rt (min): 290/0.24 64 [00665] LCMS: [M + H].sup.+/Rt (min): 288/0.31 65 [00666] LCMS: [M + H].sup.+/Rt (min): 288/0.32 66 [00667] LCMS: [M + H].sup.+/Rt (min): 316/0.35 67 [00668] LCMS: [M + H].sup.+/Rt (min): 290/0.38 68 [00669] LCMS: [M + H].sup.+/Rt (min): 304/0.32 69 [00670] LCMS: [M + H].sup.+/Rt (min): 316/0.36 70 [00671] LCMS: [M + H].sup.+/Rt (min): 320/0.36 71 [00672] LCMS: [M + H].sup.+/Rt (min): 370/0.48 72 [00673] LCMS: [M + H].sup.+/Rt (min): 328/0.51 73 [00674] LCMS: [M + H].sup.+/Rt (min): 328/0.39 74 [00675] LCMS: [M + H].sup.+/Rt (min): 316/0.49 75 [00676] LCMS: [M + H].sup.+/Rt (min): 316/0.46 76 [00677] LCMS: [M + H].sup.+/Rt (min): 262/0.15 77 [00678] LCMS: [M + H].sup.+/Rt (min): 274/0.15 78 [00679] LCMS: [M + H].sup.+/Rt (min): 276/0.24 79 [00680] LCMS: [M + H].sup.+/Rt (min): 348/0.66

Reference Example 58: (1S,6R)-2,2-difluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

Reference Example 59: (3S)-1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-methyl-N-(propan-2-yl)pyrrolidin-1-amine

Reference Example 60: (1R,6S)-2,2-difluoro-6-{4-[(propan-2-yl)oxy]piperidin-1-yl}cyclohexan-1-amine

Reference Example 61: (1R,6S)-2,2-difluoro-6-[(2S)-2-methyl-4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

Reference Example 62: (1R,6S)-2,2-difluoro-6-[(2R)-2-methyl-4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

Reference Example 63: (1S,2R)-3,3-difluoro-N.SUP.1.-methyl-N.SUP.1.-[1-(propan-2-yl)piperidin-4-yl]cyclohexan-1,2-diamine

Reference Example 64: (1R,6S)-2,2-difluoro-6-[4-(pyrrolidin-1-yl)piperidin-1-yl]cyclohexan-1-amine

Reference Example 65: (1R,6S)-2,2-difluoro-6-[5-(propan-2-yl)hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]cyclohexan-1-amine

Reference Example 66: (1R,6S)-2,2-difluoro-6-[2-(propan-2-yl)-2,8-diazaspiro[4.5]decan-8-yl]cyclohexan-1-amine

Reference Example 67: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N,N-diethylpiperidin-4-amine

Reference Example 68: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N,4-dimethyl-N-(propan-2-yl)piperidin-4-amine

Reference Example 69: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-methyl-N-[(1-methylcyclopropyl)methyl]piperidin-4-amine

Reference Example 70: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-[(1-fluorocyclopropyl)methyl]-N-methylpiperidin-4-amine

Reference Example 71: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-methyl-N-{[1-(trifluoromethyl)cyclopropyl]methyl}piperidin-4-amine

Reference Example 72: (1R,3R,5S)-8-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-(cyclopropylmethyl)-N-methyl-8-azabicyclo[3.2.1]octan-3-amine

Reference Example 73: (1R,3S,5S)-8-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-(cyclopropylmethyl)-N-methyl-8-azabicyclo[3.2.1]octan-3-amine

Reference Example 74: (4S)-1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-(cyclopropylmethyl)-N-methylazepan-4-amine

Reference Example 75: (4R)-1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-(cyclopropylmethyl)-N-methylazepan-4-amine

Reference Example 76: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-methyl-N-(propan-2-yl)azetidin-3-amine

Reference Example 77: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-(cyclopropylmethyl)-N-methylazetidin-3-amine

Reference Example 78: (1R,6S)-2,2-difluoro-6-[4-(propan-2-yl)-1,4-diazepan-1-yl]cyclohexan-1-amine

Reference Example 79: tert-butyl {1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]piperidin-4-yl}methylcarbamate

Reference Example 80

N-{(1R,6S)-2,2-Difluoro-6-[4-(methylamino)piperidin-1-yl]cyclohexyl}-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carboxamide

[0770] ##STR00681##

Step (i):

[0771] The title compound 136 (2.92 g) was prepared in the same manner as Example 19 by using the compound of Reference example 79 (2.61 g).

Step (ii):

[0772] To a solution of Compound 136 (2.92 g) in toluene (24 ml) was added TFA (5.56 g), and the mixture was stirred at room temperature for 3.5 hours. The reaction solution was concentrated in vacuo, the obtained residue was dissolved in water, and aqueous sodium bicarbonate was added to the solution. The mixture was extracted with chloroform, and the organic layer was concentrated in vacuo to give the title compound 137 (2.38 g).

[0773] LCMS: [M+H].sup.+/Rt (min):499/0.49 (Method C)

Reference Example 81

(1S,2R)-3,3-Difluoro-N.SUP.1.-methyl-N.SUP.1.-[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]cyclohexan-1,2-diamine

[0774] ##STR00682##

Step (i):

[0775] Compound 138 (2.61 g) was prepared in the same manner as Step (ii) in Reference example 18, by using Cert-butyl (3S)-3-(methylamino)pyrrolidine-1-carboxylate instead of 1-isopropylpiperazine at Step (ii) in Reference example 18.

Step (ii):

[0776] The title compound 139 (2.59 g) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 138 (2.61 g).

Step (ii):

[0777] The title compound 140 (1.97 g) was prepared in the same manner as Step (iii) in Reference example 42 by using Compound 139 (2.59 g) and acetone (3.87 mL).

Step (iv):

[0778] The title compound 141 (925 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 140 (1.97 g).

[0779] LCMS: [M+H].sup.+/Rt (min): 276/0.15

Reference Examples 82-88

[0780] The compounds of Reference examples 82-88 shown in the table below were prepared in the same manner as Reference example 81, by using the appropriate starting compound (Material A) instead of Cert-butyl (3S)-3-(methylamino)pyrrolidine-1-carboxylate at Step (i) in Reference example 81, and each appropriate starting compound (Material B) instead of acetone at Step (iii) in Reference example 81.

TABLE-US-00018 Instrumental Reference Chemical analytical example Material A Material B structure data 82 [00683] [00684] [00685] LCMS: [M + H].sup.+/Rt (min): 276/0.28 83 [00686] [00687] [00688] LCMS: [M + H].sup.+/Rt (min): 276/0.16 84 [00689] [00690] [00691] LCMS: [M + H].sup.+/Rt (min): 290/0.34 85 [00692] [00693] [00694] LCMS: [M + H].sup.+/Rt (min): 274/0.30 86 [00695] [00696] [00697] LCMS: [M + H]+/Rt (min): 290/0.37 87 [00698] [00699] [00700] LCMS: [M + H]+/Rt (min): 288/0.36 88 [00701] [00702] [00703] LCMS: [M + H]+/Rt (min): 293/0.33

Reference Example 82: (3R)-1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-methyl-N-(propan-2-yl)pyrrolidin-1-amine

Reference Example 83: (1S,2R)-3,3-difluoro-N.SUP.1.-methyl-N.SUP.1.-[(3R)-1-(propan-2-yl)pyrrolidin-3-yl]cyclohexan-1,2-diamine

Reference Example 84: 1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-methyl-N-(propan-2-yl)piperidin-4-amine

Reference Example 85: (3S)-1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-cyclopropyl-N-methylpyrrolidin-1-amine

Reference Example 86: (3S)-1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-methyl-N-(2-methylpropyl)pyrrolidin-1-amine

Reference Example 87: (3S)-1-[(1S,2R)-2-amino-3,3-difluorocyclohexyl]-N-(cyclopropylmethyl)-N-methylpyrrolidin-1-amine

Reference Example 88: (1S,6S)-2,2-difluoro-6-{[1-(propan-2-yl)piperidin-4-yl]sulfanyl}oyclohexan-1-amine

Reference Example 89

(1S,2R)—N.SUP.1.-Benzyl-3,3-difluoro-N.SUP.1.-[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]cyclohexan-1,2-diamine

[0781] ##STR00704##

Step (i):

[0782] Compound 142 (2.19 g) was prepared in the same manner as Step (ii) in Reference example 18, by using Cert-butyl (3S)-3-aminopyrrolidine-1-carboxylate instead of 1-isopropylpiperazine at Step (ii) in Reference example 18.

Step (ii):

[0783] The title compound 143 (240 mg) was prepared in the same manner as Step (iii) in Reference example 42 by using Compound 142 (990 mg) and benzaldehyde (312 mg).

Step (iii):

[0784] The title compound 144 (161 mg) was prepared in the same manner as Step (ii) and Step (iii) in Reference example 81 by using Compound 143 (235 mg).

Step (iv):

[0785] The title compound 145 (87.4 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 144 (158 mg).

[0786] LCMS: [M+H].sup.+/Rt (min): 352/0.42 (Method C)

Reference Example 90

Benzyl {(1S,2R)-3,3-difluoro-2-[(4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine-1-carbonyl)amino]cyclohexyl}[(3S)-1-(propan-2-yl)pyrrolidin-3-yl]carbamate

[0787] ##STR00705## ##STR00706##

Step (i):

[0788] To a solution of Compound 142 (680 mg) in a mixture of dioxane and water (10 mL/3.3 mL) were added benzyl chloroformate (345 mg) and sodium acetate (116 mg) at 0° C., and the reaction solution was refluxed for 2 hours. After the reaction was completed, the reaction solution was extracted with chloroform. The organic layer was concentrated in vacuo to give the title compound 146 (530 mg).

Step (ii):

[0789] The title compound 147 (256 mg) was prepared in the same manner as Step (ii) and Step (iii) in Reference example 81 by using Compound 146 (530 mg).

Step (iii):

[0790] The title compound 148 (137 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 147 (254 mg).

Step (iv):

[0791] The title compound 149 (175 mg) was prepared in the same manner as Example 19 by using Compound 148 (135 mg).

[0792] LCMS: [M+H].sup.+/Rt (min): 647/0.79 (Method C)

Reference Example 91

(1R,6S)-2,2-Difluoro-6-[5-(propan-2-yl)-1,2,4-oxadiazol-3-yl]cyclohexan-1-amine

[0793] ##STR00707##

Step (i):

[0794] To a solution of Compound 49 (2.01 g) in acetonitrile (12.6 ml) were added sodium cyanide (495 mg) and lithium perchlorate (67 mg), and the reaction solution was refluxed for 3 hours. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 150 (2.05 g).

Step (ii):

[0795] The title compound 151 (1.88 g) was prepared in the same manner as Step (i) in Reference example 8 by using Compound 150 (2.04 g).

Step (iii):

[0796] The title compound 152 (89.7 mg) was prepared in the same manner as Step (ii) and Step (iii) in Reference example 8 by using Compound 151 (200 mg) and isobutyric acid (53.6 mg).

Step (iv):

[0797] The title compound 153 (41.5 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 152 (87.7 mg).

[0798] LCMS: [M+H].sup.+/Rt (min): 246/0.37 (Method C)

Reference Example 92

(1R,6S)-2,2-Difluoro-6-[4-(propan-2-yl)-1H-1,2,3-triazol-1-yl]cyclohexan-1-amine

[0799] ##STR00708##

Step (i):

[0800] To a solution of Compound 49 (1.6 g) in a mixture of acetonitrile and water (23 mL/2.5 mL) was added sodium azide (490 mg), and the reaction solution was heated at 70° C. for 1.5 hours. After the reaction was completed, saturated aqueous sodium bicarbonate was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 154 (1.78 g).

Step (ii):

[0801] To a solution of Compound 154 (550 mg) in a mixture of methanol and THF (11.4 mL/2.3 mL/4 mL) were added sodium ascorbate (30.2 mg), tris(2-benzimidazolylmethyl)amine (46.5 mg), and 3-methylbut-1-yne (156 mg). A solution of copper sulfate (18.2 mg) in water (3.8 mL) was added to the reaction solution, and the reaction mixture was stirred at room temperature. After the reaction was completed, the reaction mixture was filtrated with Celite, and concentrated in vacuo. Then, the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 155 (353 mg).

Step (iii):

[0802] The title compound 156 (168 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 155 (353 mg).

[0803] LCMS: [M+H].sup.+/Rt (min): 245/0.42

Reference Example 93

(1R,6S)-2,2-Difluoro-6-[4-(2-methylpropyl)-1H-1,2,3-triazol-1-yl]cyclohexan-1-amine

[0804] The compound of Reference example 93 shown in the table below was prepared according to the process in the above Reference example 92 by using 4-methylpent-1-yne instead of 3-methylbut-1-yne at Step (ii) in Reference example 92.

TABLE-US-00019 Instrumental Reference analytical example Chemical structure data 93 [00709] LCMS: [M + H].sup.+/Rt (min): 259/0.51

Reference Example 94

[(1S,2R)-2-Amino-3,3-difluorocyclohexyl][4-(propan-2-yl)piperazin-1-yl]methanone

[0805] ##STR00710##

Step (i):

[0806] To a solution of Compound 150 (555 mg) in DMSO (6 mL) was added aqueous hydrochloric acid (9 mL), and the reaction solution was heated at 120° C. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and concentrated in vacuo to give the title compound 157 (600 mg).

Step (ii):

[0807] To a solution of Compound 157 (476 mg) in DMF (1.5 mL) were added 1-isopropylpiperazine (234 mg), triethylamine (308 mg), and HATU (753 mg), and the reaction solution was stirred at room temperature. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 158 (610 mg).

[0808] LCMS: [M+H].sup.+/Rt (min): 475/0.59

Step (iii):

[0809] The title compound 159 (180 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 158 (605 mg).

[0810] LCMS: [M+H].sup.+/Rt (min): 290/0.16

Reference Example 95

(1R,6R)-2,2-Difluoro-6-{[4-(propan-2-yl)piperazin-1-yl]methyl}cyclohexan-1-amine

[0811] ##STR00711##

Step (i):

[0812] The title compound 160 (112 mg) was prepared in the same manner as Step (ii) in Reference example 22 by using Compound 159 (171 mg).

[0813] LCMS: [M+H].sup.+/Rt (min): 276/0.24

Reference Examples 96-114

[0814] The compounds of Reference examples shown in the table below were prepared according to the process in the above Reference example 37, by using each appropriate starting compound instead of (S)-1-isopropylpyrrolidin-3-ol at Step (i) in Reference example 37.

TABLE-US-00020 Instrumental Reference analytical example Chemical structure data  96 [00712] LCMS: [M + H].sup.+/Rt (min): 277/0.30  97 [00713] LCMS: [M + H].sup.+/Rt (min): 278/0.57  98 [00714] LCMS: [M + H].sup.+/Rt (min): 260/0.45  99 [00715] LCMS: [M + H].sup.+/Rt (min): 249/0.16 100 [00716] LCMS: [M + H].sup.+/Rt (min): 303/0.32 101 [00717] LCMS: [M + H].sup.+/Rt (min): 303/0.33 102 [00718] LCMS: [M + H].sup.+/Rt (min): 303/0.31 103 [00719] LCMS: [M + H].sup.+/Rt (min): 303/0.32 104 [00720] LCMS: [M + H].sup.+/Rt (min): 275/0.43 105 [00721] LCMS: [M + H].sup.+/Rt (min): 277/0.38 106 [00722] LCMS: [M + H].sup.+/Rt (min): 293/0.36 107 [00723] LCMS: [M + H].sup.+/Rt (min): 291/0.16 (Method C) 108 [00724] LCMS: [M + H].sup.+/Rt (min): 275/0.49 109 [00725] LCMS: [M + H].sup.+/Rt (min): 291/0.20 (Method C) 110 [00726] LCMS: [M + H].sup.+/Rt (min): 289/0.32 111 [00727] LCMS: [M + H].sup.+/Rt (min): 293/0.26 112 [00728] LCMS: [M + H].sup.+/Rt (min): 343/0.37 113 [00729] LCMS: [M + H].sup.+/Rt (min): 295/0.37 114 [00730] LCMS: [M + H].sup.+/Rt (min): 305/0.15

Reference Example 96: (1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)piperidin-4-yl]oxy}cyclohexan-1-amine

Reference Example 97: (1R,6S)-2,2-difluoro-6-{[3-(propan-2-yl)-1,2,4-thiadiazol-5-yl]oxy}cyclohexan-1-amine

Reference Example 98: (1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)-1H-pyrazol-4-yl]oxy}cyclohexan-1-amine

Reference Example 99: (1R,6S)-2,2-difluoro-6-{[1-(propan-2-yl)azetidin-3-yl]oxy}cyclohexan-1-amine

Reference Example 100: (1R,6S)-2,2-difluoro-6-{[(1R,3S,5S)-8-(propan-2-yl)-8-azabicyclo[3.2.1]octan-3-yl]oxy}cyclohexan-1-amine

Reference Example 101: (1R,6S)-2,2-difluoro-6-{[(1R,5S,8R)-3-(propan-2-yl)-3-azabicyclo[3.2.1]octan-8-yl]oxy}cyclohexan-1-amine

Reference Example 102: (1R,6S)-2,2-difluoro-6-{[(1R,5S,8S)-3-(propan-2-yl)-3-azabicyclo[3.2.1]octan-8-yl]oxy}cyclohexan-1-amine

Reference Example 103: (1R,6S)-2,2-difluoro-6-{[(1R,3R,5S)-8-(propan-2-yl)-8-azabicyclo[3.2.1]octan-3-yl]oxy}cyclohexan-1-amine

Reference Example 104: (1R,6S)-2,2-difluoro-6-{[(1R,5S,6S)-3-(propan-2-yl)-3-azabicyclo[3.1.0]hexan-6-yl]oxy}cyclohexan-1-amine

Reference Example 105: (1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexan-1-amine

Reference Example 106: (1R,6S)-2,2-difluoro-6-{[(3R,4R)-4-methoxy-1-(propan-2-yl)pyrrolidin-3-yl]oxy}cyclohexan-1-amine

Reference Example 107: (1R,6S)-2,2-difluoro-6-{[4-methyl-1-(propan-2-yl)piperidin-4-yl]oxy}cyclohexan-1-amine

Reference Example 108: (1R,6S)-6-{[(3S)-1-(cyclopropylmethyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexan-1-amine

Reference Example 109: (1R,6S)-6-{[(3S)-1-(2,2-dimethylpropyl)pyrrolidin-3-yl]oxy}-2,2-difluorocyclohexan-1-amine

Reference Example 110: (1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-methylcyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexan-1-amine

Reference Example 111: (1R,6S)-2,2-difluoro-6-({(3S)-1-[(1-fluorocyclopropyl)methyl]pyrrolidin-3-yl}oxy)cyclohexan-1-amine

Reference Example 112: (1R,6S)-2,2-difluoro-6-{[(3S)-1-{[1-(trifluoromethyl)cyclopropyl]methyl}pyrrolidin-3-yl]oxy}cyclohexan-1-amine

Reference Example 113: (1R,6S)-2,2-difluoro-6-{[(3S)-1-(2-fluoro-2-methylpropyl)pyrrolidin-3-yl]oxy}cyclohexan-1-amine

Reference Example 114: (1R,6S)-2,2-difluoro-6-({(3S)-1-[(3-methyloxetan-3-yl)methyl]pyrrolidin-3-yl}oxy)cyclohexan-1-amine

Reference Examples 115-118

[0815] The compounds of Reference examples 115-118 shown in the table below were prepared in the same manner as Reference example 8, by using the appropriate starting compound (Material A) instead of Compound 26 at Step (i) in Reference example 8, and each appropriate starting compound (Material B) instead of cyclopropane-carboxylic acid at Step (iii) in Reference example 8.

TABLE-US-00021 Instrumental Reference Chemical analytical example Material A Material B structure data 115 [00731] [00732] [00733] LCMS: [M + H].sup.+/Rt (min): 226/0.29 (Method C) 116 [00734] [00735] [00736] LCMS: [M + H].sup.+/Rt (min): 226/0.29 (Method C) 117 [00737] [00738] [00739] LCMS: [M + H].sup.+/Rt (min): 220/0.43 (Method C) 118 [00740] [00741] [00742] LCMS: [M + H].sup.+/Rt (min): 240/0.39 (Method C)

Reference Example 115: 4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine

Reference Example 116: 4-{5-[(1R,2R)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}-4-methylpiperidine

Reference Example 117: 4-(5-cyclobutyl-1,2,4-oxadiazol-3-yl)-4-methylpiperidine monohydrochloride

Reference Example 118: 4-ethyl-4-{5-[(1S,2S)-2-fluorocyclopropyl]-1,2,4-oxadiazol-3-yl}piperidine

Reference Example 119

(1R,6S)-2,2-Difluoro-6-{[2-(propan-2-yl)pyrimidin-4-yl]oxy}cyclohexan-1-amine

[0816] ##STR00743##

Step (i):

[0817] To a solution of Compound 161 (148 mg) known in literature in THF (3 ml) were added sodium hydride (55%, 30 mg) at 0° C., and then 4-chloro-2-(propan-2-yl)pyrimidine. The reaction solution was warmed to room temperature and stirred. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 162 (209 mg).

Step (ii):

[0818] To a solution of Compound 162 (113 mg) in ethyl acetate (2 mL) was added palladium hydroxide (17 mg) at room temperature, and the mixture was stirred under hydrogen atmosphere. After the reaction was terminated as judged by LC-MS, the reaction mixture was filtrated with Celite, and the filtrate was concentrated in vacuo to give the title compound 163 (33.5 mg).

[0819] LCMS: [M+H].sup.+/Rt (min): 272/0.47

Reference Example 120

(1R,6S)-2,2-Difluoro-N-methyl-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

[0820] ##STR00744##

Step (i):

[0821] To a solution of Compound 50 (173 mg) in DMF (3 mL) were added cesium carbonate (253 mg) and methyl iodide (72 mg) at 0° C., and then the reaction mixture was warmed to room temperature and stirred. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 164 (159 mg).

Step (ii):

[0822] The title compound 165 (71 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 164 (134 mg).

[0823] LCMS: [M+H].sup.+/Rt (min): 276/0.15

Reference Example 121

rac-(1S,6S)-2,2-Dimethyl-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

[0824] ##STR00745##

Step (i):

[0825] To a solution of Compound 166 (283 mg) in 2-propanol (8 ml) was added aqueous ammonia (6 g), and the reaction mixture was refluxed. After the reaction was terminated as judged by the consumption of the starting material, the reaction solution was concentrated in vacuo to be used in the next step.

Step (ii):

[0826] The title compound 168 (64.3 mg) was prepared in the same manner as Step (i) in Reference example 18 by using Compound 167.

Step (iii):

[0827] The title compound 169 (102 mg) was prepared in the same manner as Step (ii) in Reference example 18 by using Compound 168 (60.8 mg).

Step (iv):

[0828] The title compound 170 (40.2 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 169 (102 mg).

[0829] LCMS: [M+H].sup.+/Rt (min): 254/0.43

Reference Example 122

rac-(1S,2S)-2-[4-(Propan-2-yl)piperazin-1-yl]cycloheptan-1-amine

[0830] The compounds of Reference examples shown in the table below were prepared according to the process in the above Reference example 120, by using 8-oxabicyclo[5.1.0]octane instead of Compound 166 at Step (i) in Reference example 120.

TABLE-US-00022 Instrumental Reference analytical example Chemical structure data 122 [00746] LCMS: [M + H].sup.+/Rt (min): 240/0.24

Reference Example 123

rac-(1R,2R,6S)-2-Fluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

[0831] ##STR00747##

Step (i):

[0832] A solution of Compound 171 (403 mg) and tetrabutylammonium dihydrogen trifluoride (1.78 g) in toluene (1 mL) was heated at 150° C. with a microwave device. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 172 (323 mg).

Step (ii):

[0833] Compound 172 (457 mg) was dissolved in THF (4.1 mL). To the solution were added triethylamine (1.13 mL) and methanesulfonyl chloride (0.318 mL) under ice temperature, and the reaction mixture was stirred. After the reaction was terminated as judged by the consumption of the starting material, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 173 (578 mg).

Step (iii):

[0834] To a solution of Compound 173 (571 mg) in ethanol (3.5 mL) was added palladium hydroxide (20%, 133 mg) at room temperature, and the mixture was stirred under hydrogen atmosphere. After the reaction was completed, the reaction mixture was filtrated with Celite, and the filtrate was concentrated in vacuo. The obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 174 (400 mg).

Step (iv):

[0835] Compound 174 (176 mg) was dissolved in 1,4-dioxane (3.5 mL). To the solution was added DBU (0.25 mL), and the reaction mixture was stirred at 85° C. After the reaction was terminated as judged by the consumption of the starting material, the reaction mixture was subsequently reacted in the same manner as Step (i) in Reference example 121, and methanesulfonylated in the same manner as the present Step (ii). Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound 175 (86 mg).

Step (v):

[0836] The title compound 176 (92.8 mg) was prepared according to the cyclization condition of Step (ii) in Reference example 121 followed by the same manner as Step (ii) in Reference example 18 by using Compound 175 (86 mg).

Step (vi):

[0837] The title compound 177 (35.1 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 176 (86.1 mg).

[0838] LCMS: [M+H].sup.+/Rt (min): 244/0.19

Reference Example 124

rac-(1R,2S,6S)-2-Fluoro-6-[4-(propan-2-yl)piperazin-1-yl]cyclohexan-1-amine

[0839] ##STR00748##

Step (i):

[0840] The title compound 179 (953 mg) was prepared in the same manner as Step (i) in Reference example 123 by using Compound 178 (929 mg).

Step (ii):

[0841] Compound 179 (283 mg) was dissolved in chloroform (6 mL). To the solution were added pyridine (0.51 mL) and trifluoromethanesulfonic anhydride (0.256 mL) under ice temperature, and the reaction mixture was stirred. After the reaction was terminated as judged by the consumption of the starting material, aqueous sodium bicarbonate was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 180 (424 mg).

Step (iii):

[0842] To a solution of Compound 180 (418 mg) in DMF (4 mL) was added sodium azide (229 mg), and the reaction solution was stirred at room temperature. After the reaction was completed, water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 181 (102 mg).

Step (iv):

[0843] To a solution of Compound 181 (102 mg) in ethanol (2 mL) was added palladium hydroxide (20%, 58 mg) at room temperature, and the mixture was stirred under hydrogen atmosphere. The reaction mixture was filtrated with Celite, and the filtrate was concentrated in vacuo. The obtained residue was dissolved in ethanol (2 mL) again, and aqueous hydrogen chloride (cyclopentylmethyl solution, 5 M, 0.327 mL) and palladium carbon (10%, 71 mg) were added thereto. The mixture was stirred under hydrogen atmosphere. After the reaction was completed, the reaction mixture was filtrated with Celite, and the filtrate was concentrated in vacuo to give the title compound 182 (76.8 mg).

Step (v):

[0844] The title compound 183 (69 mg) was prepared in the same manner as Step (i) and Step (ii) in Reference example 18 by using Compound 182 (103 mg).

Step (vi):

[0845] The title compound 184 (34.3 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 183 (72 mg).

[0846] LCMS: [M+H].sup.+/Rt (min): 244/0.14

Reference Example 125

(1S,2R)-2-Amino-3,3-difluorocyclohexyl 4-(propan-2-yl)piperazine-1-carboxylate

[0847] ##STR00749##

Step (i):

[0848] To a solution of Compound 185 known in literature in acetonitrile (3 mL) was added Boc.sub.2O (238 mg), and the reaction solution was stirred at room temperature. After the reaction was completed, the reaction mixture was concentrated in vacuo, and the obtained residue was purified by silica gel column chromatography (eluate: hexane/ethyl acetate) to give the title compound 186 (216 mg).

Step (ii):

[0849] The title compound 187 (118 mg) was prepared in the same manner as Step (iii) in Reference example 2 by using Compound 186 (95.7 mg).

Step (iii):

[0850] The title compound 188 (99.7 mg) was prepared in the same manner as Step (iv) in Reference example 2 by using Compound 187 (118 mg).

[0851] LCMS: [M+H].sup.+/Rt (min): 306/0.25

Reference Example 126

N-{(1S,6S)-2,2-Difluoro-6-[1-(propan-2-yl)piperidine-4-sulfonyl]cyclohexyl}-4-nitrobenzene-1-sulfonamide

[0852] ##STR00750##

Step (i):

[0853] The title compound 189 (402 mg) was prepared in the same manner as Step (ii) in Reference example 18 by using Compound 49 (399 mg) and Cert-butyl 4-sulfanylpiperidine-1-carboxylate (300 mg).

Step (ii):

[0854] To a solution of Compound 189 (210 mg) in chloroform (2 mL) was added m-CPBA (242 mg), and the reaction solution was stirred at room temperature. After the reaction was completed, aqueous sodium thiosulfate was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, concentrated in vacuo, and then the obtained residue was purified by amino silica gel column chromatography (eluate: chloroform/methanol) to give the title compound 190 (250 mg).

Step (iii):

[0855] The title compound 191 (223 mg) was prepared in the same manner as Step (i) and Step (ii) in Reference example 53 by using Compound 190 (250 mg).

Step (iv):

[0856] The title compound 192 (102 mg) was prepared in the same manner as Step (iii) in Reference example 18 by using Compound 191 (223 mg).

[0857] LCMS: [M+H].sup.+/Rt (min): 325/0.21

Test 1: Evaluation of Agonist Activity for Orexin Receptor Type 2

[0858] Human orexin receptor type 2 and apoaequorin were transiently expressed in CHO cells, and the agonist activity was evaluated based on intracellular calcium mobilization with ligand stimulation. The CHO cells transiently-expressed human orexin receptor type 2 and apoaequorin were seeded on a 384-well plate by 2,000 cells/well, and then incubated for 16-22 hours. After the plate was returned to room temperature, Coelenterazine hcp (final concentration: 1 μM) was added to the plate, and the plate was allowed to stand at room temperature for 2 hours. And then, Orexin A (PEPTIDE INSTITUTE, INC., Lot. 641114) or each test compound was added to the plate, and the luminescence of the cells was measured with FDSS7000 (Hamamatsu Photonics K.K.), wherein Orexin A and each test compound were dissolved in DMSO (final concentration: 0.1%), and diluted with a buffer (Hanks, 20 mM HEPES, 0.1% BSA). The agonist activity of each test compound for orexin receptor type 2 was calculated as relative percentage of luminescence for the luminescence (100%) of Orexin A (100 pM).

Result:

[0859] The results that each compound obtained in Examples was evaluated about the agonist activity for orexin receptor type 2 showed that the present compounds have agonist activity for orexin receptor type 2. Each agonist activity of the example compounds is shown in the table below as relative percentage of luminescence for the luminescence (100%) of Orexin A (100 pM).

TABLE-US-00023 Example agonist activity (%) 1 137 2 58 3 67 4 62 5 103 6 43 7 75 8 207 9 207 10 213 11 211 12 178 13 56 14 178 15 62 16 39 17 72 18 73 19 167 20 160 21 153 22 163 23 104 24 210 25 165 26 198 27 162 28 190 29 109 30 128 31 168 32 176 33 123 34 183 35 165 36 114 37 45 38 142 39 157 41 23 42 141 43 146 44 148 45 150 46 136 47 163 48 156 49 151 50 154 51 149 52 113 53 143 54 146 55 95 56 140 57 155 58 150 59 164 60 151 61 169 62 174 63 149 64 204 65 155 66 144 67 175 68 156 69 161 70 141 71 199 72 146 73 185 74 174 75 141 76 145 77 158 78 36 79 191 80 178 81 57

Test 2: Evaluation of Agonist Activity for Orexin Receptor Type 2

[0860] Human orexin receptor type 2 and apoaequorin were transiently expressed in CHO cells, and the agonist activity was evaluated based on intracellular calcium mobilization with ligand stimulation. The CHO cells transiently-expressed human orexin receptor type 2 and apoaequorin were seeded on a 384-well plate by 2,000 cells/well, and then incubated for 16-22 hours. After the plate was returned to room temperature, Coelenterazine hcp (final concentration: 1 μM) was added to the plate, and the plate was allowed to stand at room temperature for 2 hours. And then, Orexin A (PEPTIDE INSTITUTE, INC., Lot. 671009) or each test compound was added to the plate, and the luminescence of the cells was measured with FDSS7000 (Hamamatsu Photonics K.K.), wherein Orexin A and each test compound were dissolved in DMSO (final concentration: 0.1%), and diluted with a buffer (Hanks, 20 mM HEPES, 0.1% BSA). The agonist activity of each test compound for orexin receptor type 2 was calculated as relative percentage of luminescence for the luminescence (100%) of Orexin A (100 pM).

Result:

[0861] The results that each compound obtained in Examples was evaluated about the agonist activity for orexin receptor type 2 showed that the present compounds have agonist activity for orexin receptor type 2. Each agonist activity of the example compounds is shown in the table below as relative percentage of luminescence for the luminescence (100%) of Orexin A (100 pM).

TABLE-US-00024 Example agonist activity (%) 82 69 83 371 84 372 85 360 86 367 87 226 88 201 89 0 90 112 91 243 92 16 93 365 94 382 95 447 96 493 97 486 98 271 99 499 100 340 101 326 102 374 103 369 104 289 105 359 106 220 107 363 108 292 109 359 110 380 111 382 112 376 113 374 114 438 115 403 116 488 117 465 118 524 119 378 120 387 121 379 122 369 123 366 124 391 125 402 126 394 127 367 128 402 129 435 130 450 131 461 132 166 133 506 134 456 135 396 136 346 137 376 138 385 139 351 140 249 141 405 142 407 143 444 144 399 145 403 146 23 147 373 148 391 149 419 150 437 151 368 152 470 153 350 154 493 155 167 156 323 157 392 158 389 159 392 160 410 161 374

INDUSTRIAL APPLICABILITY

[0862] The compounds of the present invention exhibit a potent agonist activity for orexin receptor, thereby they are useful as a medicament for treating or preventing narcolepsy, idiopathic hypersomnia, hypersomnia, sleep apnea syndrome, narcolepsy syndrome involving narcolepsy-like symptom, hypersomnia associated with Parkinson's disease, hypersomnia associated with dementia with Lewy body, etc.