COMPOUNDS FOR INHIBITION OF FIBROBLAST ACTIVATION PROTEIN
20230192647 · 2023-06-22
Assignee
Inventors
- Adela SIMKOVA (Praha 8, CZ)
- Pavel SACHA (Praha 6, CZ)
- Natan SIDEJ (Praha 8, CZ)
- Tereza ORMSBY (Praha 1, CZ)
- Jan KONVALINKA (Praha 6, CZ)
Cpc classification
C07K5/06026
CHEMISTRY; METALLURGY
A61K51/0478
HUMAN NECESSITIES
A61K51/0497
HUMAN NECESSITIES
A61P35/00
HUMAN NECESSITIES
International classification
C07D401/12
CHEMISTRY; METALLURGY
A61P35/00
HUMAN NECESSITIES
Abstract
Quinolinecarboxamide compounds of general formula I exceed the previously known FAP inhibitors in affinity and inhibitory effect. These agents can be used to specifically target tumours for diagnostic and therapeutic purposes, or for laboratory purposes in the study of endogenous FAP expression.
Claims
1. Quinolinecarboxamide compounds of general formula I ##STR00038## wherein R.sub.1 and R.sub.2 are independently selected from the group consisting of H, D, and F, R.sub.3 is selected from the group consisting of H, D, and C1-C5 alkyl, R.sub.4 and R.sub.5 are independently selected from the group consisting of H, D, —OH, C1-C3 alkoxy and a structure -X-Y-Z, wherein X is oxygen or —NH—, Y is ##STR00039## wherein k is an integer from 5 to 15 and m is an integer from 1 to 3, and Z is ##STR00040## R.sub.6 is selected from the group consisting of H, D, C1-C10 alkyl, C3-C10 cycloalkyl, adamantyl, and substituted or unsubstituted aryl or C7-C20 alkylaryl, wherein the aryl is ##STR00041## wherein R.sub.7 and R.sub.11 are independently selected from the group consisting of H, D, halogen, C1-C3 alkyl, C1-C3 alkoxy, —CF.sub.3, and —C(═O)—OR.sub.12, wherein R.sub.12 is selected from the group consisting of H, D, halogen, and C1-C4 alkyl or C1-C2 alkyl, R.sub.8, R.sub.9 and R.sub.10 are independently selected from the group consisting of H, D, halogen, —OMe, C1-C3 alkyl, C1-C3 alkoxy or C1-C2 alkoxy, —CF.sub.3, and —C(═O)—OR.sub.12, or R.sub.6 is ##STR00042## wherein R.sub.13 is selected from the group consisting of —OR.sub.12, —NHR.sub.12, —N(—CH.sub.3)R.sub.12, pyrrolidine, and morpholine, R.sub.14 and R.sub.15 are independently selected from the group consisting of H, D, C1-C5 alkyl, phenyl, 3,4-dimethoxyphenyl, benzyl, 3,4-dimethoxybenzyl, and unsubstituted C3-C8 heteroalkylaryl, R16 and R17 are independently selected from the group consisting of H, D, C1-C6 alkyl, phenyl, benzyl, 4-hydroxybenzyl, unsubstituted C3-C8 heteroalkylaryl, —(CH.sub.2).sub.n—C(═O)—OR.sub.18, —(CH.sub.2).sub.n—C(═O)—NR.sub.19R.sub.20, and —(CH.sub.2).sub.n—NR.sub.21R.sub.22, wherein n is an integer from 1 to 4, R.sub.18 is selected from the group consisting of H, D, C1-C3 alkyl, and benzyl, R.sub.19 and R.sub.20 are independently selected from the group consisting of H, D, C1-C3 alkyl, benzyl, and 3,4-dimethoxybenzyl, and R.sub.21 and R.sub.22 are independently selected from the group consisting of H, D, and (benzyloxy)carbonyl.
2. Quinolinecarboxamide compounds of the general formula I according to claim 1, selected from the group consisting of (S)-N-(2-(2-(2-(Benzylamino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-(2-(2-((3,4-Dimethoxybenzyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)-quinoline-4-carboxamide, (S)-N-(2-(2-(2-((4-Fluorobenzyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-Oxo-2-(2-(2-oxo-2-(phenethylamino)acetyl)pyrrolidine-1-yl)ethyl)quinoline-4-carboxamide, (S)-N-(2-(2-(2-((3,4-Dimethoxyphenethyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-(2-(2-((4-Methoxyphenyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, Methyl(S)-4-(2-oxo-2-(1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetamido)benzoate, (S)-N-(2-(2-(2-(Cyclopropylamino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-(2-(2-(Isopropylamino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-Oxo-2-(2-(2-oxo-2-(pentylamino)acetyl)pyrrolidine-1-yl)ethyl)quinoline-4-carboxamide, Methyl (S)-(2-oxo-2-(1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetyl)glycinate, tert-Butyl (S)-(2-oxo-2-(1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetyl)glycinate, Methyl (2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetyl)alaninate, (S)-N-(2-(2-(2-((2-(Dimethylamino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-(2-(2-((2-(Ethyl(propyl)amino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-(2-(2-((2-(Isopropylamino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, (S)-N-(2-(2-(2-((2-(Benzylamino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)quinoline-4-carboxamide, Methyl (2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetyl)glycyl-L-leucinate, Methyl(2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetyl)glycyl-L-phenylalaninate, Methyl(2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetyl)glycyl-L-glutaminate, 5-Benzyl 1-methyl (2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidine-2-yl)acetyl)-glycyl-L-glutamate, Benzyl N.sup.6-((benzyloxy)carbonyl)-N.sup.2-(2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)-pyrrolidine-2-yl)acetyl)glycyl)-L-lysinate, (S)-S-(62-((4-((2-(2-(2-((3,4-dimethoxybenzyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl) carbamoyl)quinoline-7-yl)oxy)-2,5,8,11,61-pentaoxo-15,18,21,24,27,30,33,36,39,42,45,48,51, 54,57-pentadekaoxa-3,6,9,12,60-pentaaza-dohexacontyl)-ethanethioate, and (S)-N-(2-(2-(2-((3,4-dimethoxybenzyl)amino)-2-oxoacetyl)pyrrolidine-1-yl)-2-oxoethyl)-7-(2-(6-hydrazinylnicotinamido)ethoxy)quinoline-4-carboxamide.
3. A method of administering a medicament, comprising the step of administering quinolinecarboxamide compounds of the general formula I according to claim 1 to a subject in need thereof.
4. A method of administering a medicament, comprising the step of administering quinolinecarboxamide compounds of the general formula I according to claim 1 in treatment of cancer to a subject in need thereof.
5. A method of administering a medicament, comprising the step of administering quinolinecarboxamide compounds of the general formula I according to claim 1 in treatment of epithelial tumours to a subject in need thereof.
6. A method of administering a diagnostic composition comprising the step of administering quinolinecarboxamide compounds of the general formula I according to claim 1 in targeted diagnostics of tumour tissue.
7. A method of administering a diagnostic composition comprising the step of administering quinolinecarboxamide compounds of the general formula I according to claim 1 in targeted diagnostics of epithelial tumours.
8. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the general formula I according to claim 1 and optionally at least one pharmaceutically acceptable carrier, excipient and/or diluent.
9. A method of treating epithelia tumours comprising administering an effective amount of the composition according to claim 8 in the treatment of cancer.
10. A diagnostic composition comprising a therapeutically effective amount of a compound of the general formula I according to claim 1 and optionally at least one pharmaceutically acceptable carrier, filler and/or diluent.
11. The diagnostic composition comprising a therapeutically effective amount of a compound of the general formula I according to claim 10 in targeted diagnostics of tumour tissue.
12. The diagnostic composition comprising a therapeutically effective amount of a compound of the general formula I according to claim 10 in targeted diagnostics of epithelial tumours.
Description
EXAMPLES
[0073] List of abbreviations: [0074] bd broad dublet [0075] Bn benzyl [0076] Boc terc-butyloxycarbonyl [0077] bt broad triplet [0078] Cbz benzyloxycarbonyl [0079] CCRF-CEM human lymphoblastoid leukemia tumour cell line [0080] Cp cyclopropyl [0081] CT computed tomography [0082] d doublet [0083] DCM dichloromethane [0084] dd doublet of doublets [0085] ddd doublet of doublets of doublets [0086] DIPEA diisopropylethylamine [0087] DMF dimethylformamide [0088] DMSO dimethyl sulfoxide [0089] DOTA 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid [0090] DPPIV dipeptidyl peptidase IV [0091] ekv. molar equivalent [0092] FAP fibroblast activation protein [0093] FDG (18F)-fluorodeoxyglucose [0094] Gly glycine [0095] Hela human cervical carcinoma cell line [0096] HepG2 human liver carcinoma cell line [0097] HL-60 human myeloid leukemia cell line [0098] HPLC high-performance liquid chromatography [0099] HR MS high-resolution mass spectrum [0100] HYNIC hydrazinonicotinic acid [0101] IBX iodoxybenzoic acid [0102] IC.sub.50 mean inhibitory concentration [0103] LC-MS tandem of liquid chromatography and mass spectrometry [0104] m multiplet [0105] MAG3 mercaptoacetyltriglycine [0106] MeOH methanol [0107] NMR nuclear magnetic resonance [0108] PDA light detector with diode array [0109] PET positron emission tomography [0110] Ph phenyl [0111] PREP prolyl endopeptidase [0112] Pro proline [0113] QDA mass detector with Dalton quadrupole [0114] R.sub.t retention time [0115] s singlet [0116] SPECT single-photon emission computed tomography [0117] TFA trifluoroacetic acid [0118] TSTU N,N,N′,N′-Tetramethyl-O-(N-succinimidypuronium tetrafluoroborate [0119] UHPLC-MS tandem of ultra-high performance liquid chromatography and mass spectrometry [0120] UV ultraviolet rays [0121] vol./vol. proportion of volume units [0122] wt./wt. proportion of weight units
[0123] Instruments Used in the Synthesis of Compounds Prepared in the Examples Below
[0124] NMR spectra were measured in a Bruker Avance III 500 MHz spectrometer (.sup.1H at 500 MHz and .sup.13C at 125.7 MHz). High-resolution mass spectra (HR MS) were measured in an LTQ Orbitrap XL hybrid mass spectrometer (Thermo Fisher Scientific, Waltham, Mass., USA) using electrospray ionization. During the synthesis, the substances were purified by reversed-phase FLASH chromatography (silica gel C18 230-400 mesh) in a Teledyne ISCO CombiFLASH Rf+ with a dual UV detector (210 and 254 nm) using a gradient of 0.1% (vol./vol.) aqueous solution of trifluoroacetic acid.fwdarw.acetonitrile. Purity and conversion during the reactions were monitored by UHPLC-MS in a Waters Acquity H-class UPLC with PDA (diode array, 190-800 nm) and QDA (100-1250 m/z) detectors using a Bischoff ProntoSIL HPLC column (100×2.0 mm, Prontopearl TPP 120-2.2-C18 SH, 2.2 μm) and a gradient of water.fwdarw.acetonitrile with the addition of 0.1% (vol./vol.) formic acid at a flow rate of 0.5 ml/min.
[0125] Overview of the Compounds Prepared in the Examples Below
TABLE-US-00001 Com- Example pound Structure Systematic name 1 3a
[0126] General Procedure 1: Sequence of Passerini Reaction, Acid Deprotection and Basic Transacylation
[0127] Boc-L-prolinal (1 eq.), N-Cbz-glycine (1 eq.) and the corresponding isonitrile (1 eq.) were dissolved in anhydrous DCM, and the resulting mixture was stirred at room temperature for 4 hours. At full conversion (LC-MS), trifluoroacetic acid was added and the mixture was stirred for another hour. The mixture was concentrated under reduced vacuum and then redissolved in DCM. While stirring and cooling to 0° C., triethylamine was added dropwise to the mixture. The mixture was further stirred at room temperature until full conversion (LC-MS, maximum 3 hours). The liquid portions of the mixture were evaporated under reduced pressure and the residue was redissolved in DCM. The polar portions of the mixture were extracted into water (3×) and the organic phase was dried over brine and sodium sulfate. After evaporating the solvent, α-hydroxyamide 4 was obtained, which was used for the next reaction without purification. Reaction yields are calculated based on the amount of Boc-L-prolinal used. In General Procedure 1, a mixture of diastereomers was always obtained, the retention times of which are given as R.sub.t,1 and R.sub.t,2.
[0128] General Procedure 2: Debenzylation
[0129] The Cbz or Bn protected substance was dissolved in methanol, and palladium hydroxide on coal was added to the mixture. The mixture was placed in a hydrogen atmosphere and stirred for 3 hours. The catalyst was separated from the mixture by filtration, and the liquid portion was concentrated under reduced pressure. Residual solvent and water were removed from the mixture under high vacuum. The substance obtained in this way was used without further purification for the next reaction.
[0130] General Procedure 3: Peptide-Forming Condensation Using TSTU
[0131] The carboxylic acid (1 eq.), TSTU (1 eq.) and DIPEA were dissolved in anhydrous DMF. After stirring for 1 hour at room temperature, a solution of the amine (1.1 eq.) in anhydrous DMF was added to the mixture, and the resulting mixture was stirred overnight. The product was isolated from the crude mixture by reversed-phase FLASH chromatography. Its trifluoroacetate salt was obtained by lyophilization of the fractions containing the desired product. Reaction yields are calculated with respect to the amount of precursor 4 used. In General Procedure 3, a mixture of diastereomers was always obtained, the retention times of which are reported as R.sub.t,1 and R.sub.t,2.
[0132] General Procedure 4: Oxidation
[0133] A mixture of α-hydroxyamide (1 eq.) and IBX (1.5 eq.) in DMSO was stirred overnight. At full conversion (by LC-MS), the product was isolated from the crude mixture by reversed-phase FLASH chromatography. Its trifluoroacetate salt was obtained by lyophilization of the fractions containing the desired product. Reaction yields are calculated with respect to the amount of α-hydroxyamide 5 used. According to the NMR and LC-MS analyses, the products of General Procedure 4 are present as a mixture of rotamers. Only the set of signals belonging to the dominant rotamer is listed in the NMR reports. The retention times of both rotamers are given as R.sub.t,1 and R.sub.t,2.
[0134] Preparation of Precursor 7
[0135] Methylester 2k (500 mg, 926 μmop was dissolved in 9 ml of methanol and 1 ml of 10% (wt./wt.) aqueous KOH. After stirring at room temperature for 5 hours, the mixture was neutralized by the dropwise addition of 10% (wt./wt.) HCl to a pH between 7 and 8 and concentrated under reduced pressure. The product was isolated from the mixture directly by FLASH chromatography. Lyophilization of the fractions containing the desired product (LC-MS) gave the product trifluoroacetate as a white solid (350 mg, 72% yield; LC-MS R.sub.t,1 2.64 min, R.sub.t,2 2.71 min, m/z 415.30 [M+H].sup.+).
Example 1
(S)-N-(2-(2-(2-(Benzylamino)-2-oxoacetyl)pyrrolidin-1yl)-2-oxoethyl)quinoline-4-carboxamide
[0136] Precursor 1a (1163 mg, 79% yield; LC-MS R.sub.t,1 3.98 min, R.sub.t,2 4.03 min, m/z 426.36 [M+H].sup.+) was obtained from General Procedure 1. Precursor 1a was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give precursor 2a (825 mg, 71% yield; LC-MS R.sub.t,1 3.36 min, R.sub.t,2 3.45 min, m/z 447.26 [M+H].sup.+). Precursor 2a was oxidized to the final α-ketoamide 3a (107 mg, 47% yield) by General Procedure 4.
[0137] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.31 (bt, 1H, J.sub.NH,CH2=6.4 Hz, COCONH); 9.04 (m, 1H, NH-2′); 9.04 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 8.35 (bdd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.11 (bd, 1H, J.sub.8,7=8.5 Hz, H-8); 7.87 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.70 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.63 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 7.35-7.18 (m, 5H, H-o,m,p-Bn); 5.23 (dd, 1H, J.sub.1″,2″=9.1 and 4.7 Hz, H-1″); 4.36 and 4.32 (2×dd, 2×1H, J.sub.gem=14.8 Hz, J.sub.CH2,NH=6.4 Hz, CH.sub.2—Bn); 4.28 and 4.17 (2×dd, 2×1H, J.sub.gem=16.8 Hz, J.sub.2′,NH=6.0 Hz, H-2′); 3.74-3.62 (m, 2H, H-4″); 2.25 (m, 1H, H-2″b); 2.03 (m, 1H, H-3″b); 1.97-1.80 (m, 2H, H-3″a, 2″a);
[0138] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.57 (COCONH); 166.92 (CO-1′); 166.56 (CO-3′); 160.60 (COCONH); 149.80 (CH-2); 146.60 (C-8a); 143.79 (C-4); 138.75 (C-i-Bn); 130.85 (CH-7); 128.56 (CH-m-Bn); 128.32 (CH-8); 127.97 (CH-6); 127.57 (CH-o-Bn); 127.20 (CH-p-Bn); 126.24 (CH-5); 124.58 (C-4a); 119.41 (CH-3); 60.47 (CH-1″); 46.12 (CH.sub.2-4″); 42.31 (CH.sub.2—Bn); 41.56 (CH.sub.2-2′); 27.94 (CH.sub.2-2″); 24.81 (CH.sub.2-3″);
[0139] LC-MS R.sub.t,1 3.49 min, R.sub.t,2 3.60 min, m/z 445.27 [M+H].sup.+;
[0140] HR MS for C.sub.25H.sub.25N.sub.4O.sub.4 [M+H].sup.+ calculated 445.18703; found 445.18668.
Example 2
(S)-N-(2-(2-(2-((3,4-Dimethoxybenzyl)amino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)quinoline-4-carboxamide
[0141] Precursor 4d (1176 mg, 88% yield; LC-MS R.sub.t,1 3.79 min, R.sub.t,2 3.85 min, m/z 486.16 [M+H].sup.+) was obtained from General Procedure 1. Precursor 4d was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give precursor 2b (130 mg, 92% yield; LC-MS R.sub.t,1 3.00 min, R.sub.t,2 3.07 min, m/z 507.25 [M+H].sup.+). Precursor 2b was oxidized to the final α-ketoamide 3b by General Procedure 4 (20 mg, 53% yield).
[0142] .sup.1H NMR (500 MHz, DMSO-d6): 9.22 (bt, 1H, J.sub.NH,CH2=6.3 Hz, COCONH); 9.03-8.97 (m, 2H, NH-2′, H-2); 8.32 (dd, 1H, J.sub.5,6=8.4 Hz, J.sub.5,7=1.4 Hz, H-5); 8.09 (bd, 1H, J.sub.8,7=8.5 Hz, H-8); 7.83 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.4 Hz, H-7); 7.66 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.2 Hz, H-6); 7.57 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 6.91 (d, 1H, J.sub.2,6=2.0 Hz, H-2-Ph); 6.86 (d, 1H, J.sub.5,6=8.3 Hz, H-5-Ph); 6.79 (dd, 1H, J.sub.6.5=8.2 Hz, J.sub.6,2=2.0 Hz, H-6-Ph); 5.23 (dd, 1H, J.sub.1″,2″=9.2 and 4.7 Hz, H-1″); 4.33-4.21 (m, 3H, CH.sub.2-Ph, H-2′b); 4.15 (dd, 1H, J.sub.gem=16.7 Hz, J.sub.2′a,NH=5.9 Hz, H-2′a); 3.70 (s, 3H, CH.sub.3O-3-Ph); 3.69 (s, 3H, CH.sub.3O-4-Ph); 3.70-3.62 (m, 2H, H-4″); 2.24 (m, 1H, H-2″b); 2.01 (m, 1H, H-3″b); 1.90 (m, 1H, H-3″a); 1.84 (m, 1H, H-2″a);
[0143] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.66 (COCONH); 167.08 (CO-1); 166.56 (CO-3′); 160.48 (COCONH); 150.15 (CH-2); 148.75 (C-3-Ph); 148.05 (C-4-Ph); 147.42 (C-8a); 142.98 (C-4); 131.10 (C-1-Ph); 130.40 (CH-7); 128.89 (CH-8); 127.69 (CH-6); 126.14 (CH-5); 124.49 (C-4a); 119.75 (CH-6-Ph); 119.33 (CH-3); 111.84 (CH-5-Ph); 111.69 (CH-2-Ph); 60.40 (CH-1″); 55.70 and 55.58 (CH.sub.3O); 46.12 (CH.sub.2-4″); 42.08 (CH.sub.2-Ph); 41.54 (CH.sub.2-2′); 27.95 (CH.sub.2-2″); 24.81 (CH.sub.2-3″);
[0144] LC-MS R.sub.t,1 3.32 min, R.sub.t,2 3.44 min, m/z 505.22 [M+H].sup.+;
[0145] HR MS for C.sub.27H.sub.29N.sub.4O.sub.6 [M+H].sup.+ calculated 505.20816; found 505.20740.
Example 3
(S)-N-(2-(2-(2-((4-Fluorobenzyl)amino)-2-oxoacetyl)pyrrolidin-1yl)-2-oxoethyl)quinoline-4-carboxamide
[0146] Precursor 1c (113 mg, 51% yield; LC-MS R.sub.t,1 4.08 min, R.sub.t,2 4.14 min, m/z 444.06 [M+H].sup.+) was obtained from General Procedure 1. Precursor 1c was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give precursor 2c (70 mg, 74% yield; LC-MS R.sub.t,1 3.52 min, R.sub.t,2 3.61 min, m/z 465.01 [M+H].sup.+). Precursor 2c was oxidized to the final α-ketoamide 3c (37 mg, 65% yield) by General Procedure 4.
[0147] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.32 (bt, 1H, J.sub.NH,CH2=6.4 Hz, COCONH); 9.05 (t, 1H, J.sub.NH,2′=6.0 Hz, NH-2′); 9.04 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 8.34 (dd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.11 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.87 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.70 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.62 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 7.31 (m, 2H, H-o-Ph); 7.13 (m, 2H, H-m-Ph); 5.22 (dd, 1H, J.sub.1″,2″=9.2 and 4.7 Hz, H-1″); 4.32 (bd, 2H, J.sub.CH2,NH=6.5 Hz, CH.sub.2-Ph); 4.27 and 4.17 (2×dd, 2×1H, J.sub.gem=16.9 Hz, J.sub.2′,NH=6.0 Hz, H-2′); 3.71-3.62 (m, 2H, H-4″); 2.24 (m, 1H, H-2″b); 2.01 (m, 1H, H-3″b); 1.89 (m, 1H, H-3″a); 1.86 (m, 1H, H-2″a);
[0148] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.56 (COCONH); 166.98 (CO-1′); 166.61 (CO-3′); 161.50 (d, J.sub.C,F=242.6 Hz, C-p-Ph); 160.54 (COCONH); 149.87 (CH-2); 146.71 (C-8a); 143.72 (C-4); 134.99 (d, J.sub.C,F=3.0 Hz, C-i-Ph); 130.84 (CH-7); 129.69 (d, J.sub.C,F=8.2 Hz, CH-o-Ph); 128.33 (CH-8); 127.98 (CH-6); 126.25 (CH-5); 124.60 (C-4a); 119.43 (CH-3); 115.34 (d, J.sub.C,F=21.3 Hz, CH-m-Ph); 60.51 (CH-1″); 46.16 (CH.sub.2-4″); 41.66 (CH.sub.2-Ph); 41.59 (CH.sub.2-2′); 27.97 (CH.sub.2-2″); 24.85 (CH.sub.2-3″);
[0149] LC-MS R.sub.t,1 3.65 min, R.sub.t,2 3.78 min, m/z 462.99 [M+H].sup.+;
[0150] HR MS for C.sub.25H.sub.24FN.sub.4O.sub.4 [M+H].sup.+ calculated 463.17761; found 463.17741.
Example 4
(S)-N-(2-Oxo-2-(2-(2-oxo-2-(fenethylamino)acetyl)pyrrolidin-1ypethyl)quinoline-4-carboxamide
[0151] Precursor 1d (380 mg, 85% yield; LC-MS R.sub.t,1 4.08 min, R.sub.t,2 4.14 min, m/z 440.32 [M+H].sup.+) was obtained from General Procedure 1. Precursor 1d was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2d (286 mg, 68% yield; LC-MS R.sub.t,1 3.49 min, R.sub.t,2 3.59 min, m/z 461.30 [M+H].sup.+). Precursor 2d was oxidized to the final α-ketoamide 3d (74 mg, 67% yield) by General Procedure 4.
[0152] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.02 (t, 1H, J.sub.NH,2′=6.0 Hz, NH-2′); 9.01 (d, 1H, J.sub.2,3=4.4 Hz, H-2); 8.83 (t, 1H, J.sub.NH,CH2=6.0 Hz, COCONH); 8.34 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.09 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.84 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.68 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.58 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 7.28 (m, 2H, H-m-Ph); 7.23-7.16 (m, 3H, H-o,p-Ph); 5.20 (dd, 1H, J.sub.1″,2″=9.1 and 4.6 Hz, H-1″); 4.26 and 4.16 (2×dd, 2×1H, J.sub.gem=16.8 Hz, J.sub.2′,NH=6.0 Hz, H-2′); 3.70-3.62 (m, 2H, H-4″); 3.42-3.31 (m, 2H, CH.sub.2CH.sub.2-Ph); 2.78 (t, 2H, J.sub.CH2,CH2=7.7 Hz, CH.sub.2CH.sub.2-Ph); 2.21 (m, 1H, H-2″b); 2.00 (m, 1H, H-3″b); 1.87 (m, 1H, H-3″a); 1.77 (m, 1H, H-2″a);
[0153] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.54 (COCONH); 167.10 (CO-1′); 166.58 (CO-3′); 160.39 (COCONH); 150.12 (CH-2); 147.29 (C-8a); 143.21 (C-4); 139.27 (C-i-Ph); 130.53 (CH-7); 128.88 (CH-o-Ph); 128.78 (CH-8); 128.61 (CH-m-Ph); 127.76 (CH-6); 126.44 (CH-p-Ph); 126.19 (CH-5); 124.53 (C-4a); 119.35 (CH-3); 60.51 (CH-1″); 46.11 (CH.sub.2-4″); 41.58 (CH.sub.2-2′); 40.44 (CH.sub.2CH.sub.2-Ph); 34.83 (CH.sub.2CH.sub.2-Ph); 27.83 (CH.sub.2-2″); 24.72 (CH.sub.2-3″);
[0154] LC-MS R.sub.t,1 3.63 min, R.sub.t,2 3.73 min, m/z 459.25 [M+H].sup.+;
[0155] HR MS for C.sub.26H.sub.25N.sub.4O.sub.4 [M+H].sup.+calculated 459.20268; found 459.20258.
Example 5
(S)-N-(2-(2-(2-((3,4-Dimethoxyfenethyl)amino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)quinoline-4-carboxamide
[0156] Precursor 1e (LC-MS R.sub.t,1 3.85 min, R.sub.t,2 3.91 min, m/z 500.28 [M+H].sup.+) was obtained from General Procedure 1. Precursor 1e was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2e (260 mg, 59% yield; LC-MS R.sub.t,1 3.28 min, R.sub.t,2 3.38 min, m/z 521.27 [M+H].sup.+). Precursor 2e was oxidized to the final α-ketoamide 3e (88 mg, 88% yield) by General Procedure 4.
[0157] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.04 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 9.04 (m, 1H, NH-2′); 8.78 (bt, 1H, J.sub.NH,CH2=6.0 Hz, COCONH); 8.36 (bdd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.11 (bd, 1H, J.sub.8,7=8.4 Hz, H-8); 7.87 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.71 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.62 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 6.84 (d, 1H, J.sub.5,6=8.2 Hz, H-5-Ph); 6.78 (d, 1H, J.sub.2,6=2.0 Hz, H-2-Ph); 6.70 (dd, 1H, J.sub.6,5=8.2 Hz, J.sub.6,2=2.0 Hz, H-6-Ph); 5.21 (dd, 1H, J.sub.1″,2″=9.3 and 4.7 Hz, H-1″); 4.25 and 4.17 (2×dd, 2×1H, J.sub.gem=16.8 Hz, J.sub.2′,NH=6.1 Hz, H-2′); 3.71 (s, 3H, CH.sub.3O-3-Ph); 3.69 (s, 3H, CH.sub.3O-4-Ph); 3.70-3.60 (m, 2H, H-4″); 3.35 (m, 2H, CH.sub.2CH.sub.2-Ph); 2.72 (t, 2H, J.sub.CH2,CH2=7.4 Hz, CH.sub.2CH.sub.2-Ph); 2.21 (m, 1H, H-2″b); 2.00 (m, 1H, H-3″b); 1.85 (m, 1H, H-3″a); 1.77 (m, 1H, H-2″a);
[0158] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.57 (COCONH); 166.92 (CO-1′); 166.54 (CO-3′); 160.37 (COCONH); 149.80 (CH-2); 148.78 (C-3-Ph); 147.45 (C-4-Ph); 146.60 (C-8a); 143.82 (C-4); 131.67 (C-1-Ph); 130.86 (CH-7); 128.22 (CH-8); 127.97 (CH-6); 126.26 (CH-5); 124.59 (C-4a); 120.65 (CH-6-Ph); 119.40 (CH-3); 112.60 (CH-2-Ph); 112.03 (CH-5-Ph); 60.52 (CH-1″); 55.68 (CH.sub.3O-4-Ph); 55.54 (CH.sub.3O-3-Ph); 46.10 (CH.sub.2-4″); 41.58 (CH.sub.2-2′); 40.57 (CH.sub.2CH.sub.2-Ph); 34.33 (CH.sub.2CH.sub.2-Ph); 27.82 (CH.sub.2-2″); 24.70 (CH2-3″);
[0159] LC-MS R.sub.t,1 3.41 min, R.sub.t,2 3.52 min, m/z 519.23 [M+H].sup.+;
[0160] HR MS for C.sub.28H.sub.31N.sub.4O.sub.6 [M+H].sup.+ calculated 519.22381; found 519.22360.
Example 6
(S)-N-(2-(2-(2-((4-Methoxyphenyl)amino)-2-oxoacetyl)pyrrolidin-1yl)-2-oxoethyl)quinoline-4-carboxamide
[0161] Precursor 1f (325 mg, 79% yield; LC-MS R.sub.t,1 3.97 min, R.sub.t,2 4.04 min, m/z 464.26 [M+Na].sup.+) was obtained from General Procedure 1. Precursor if was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2f (171 mg, 40% yield; LC-MS R.sub.t,1 3.32 min, R.sub.t,2 3.45 min, m/z 463.25 [M+H].sup.+). Precursor 2f was oxidized to the final α-ketoamide 3f (77 mg, 63% yield) by General Procedure 4.
[0162] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 10.56 (s, 1H, NH-Ph); 9.04 (bt, 1H, J.sub.7NH,2′=6.0 Hz, NH-2′), 9.01 (d, 1H, J.sub.2,3=4.4 Hz, H-2); 8.33 (bdd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.09 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.83 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.74 (m, 2H, H-o-Ph); 7.68 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.58 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 6.93 (m, 2H, H-m-Ph); 5.30 (dd, 1H, J.sub.1″,2″=9.0 and 4.6 Hz, H-1″); 4.27 and 4.20 (2×dd, 2×1H, J.sub.gem=16.9 Hz, J.sub.2′,NH=6.0 Hz, H-2′); 3.73 (s, 3H, CH.sub.3O-Ph); 3.76-3.65 (m, 2H, H-4″); 2.29 (m, 1H, H-2″b); 2.04 (m, 1H, H-3″b); 2.00-1.89 (m, 2H, H-3″a, H-2″a);
[0163] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.68 (COCONH); 167.07 (CO-1′); 166.68 (CO-3′); 158.54 (COCONH); 156.35 (C-p-Ph); 150.06 (CH-2); 147.16 (C-8a); 143.28 (C-4); 130.75 (C-i-Ph); 130.57 (CH-7); 128.68 (CH-8); 127.79 (CH-6); 126.18 (CH-5); 124.52 (C-4a); 122.19 (CH-o-Ph); 119.36 (CH-3); 114.11 (CH-m-Ph); 60.38 (CH-1″); 55.42 (CH.sub.3O-Ph); 46.19 (CH.sub.2-4″); 41.56 (CH.sub.2-2′); 28.12 (CH.sub.2-2″); 24.94 (CH.sub.2-3″);
[0164] LC-MS R.sub.t,1 3.48 min, R.sub.t,2 3.62 min, m/z 461.24 [M+H].sup.+;
[0165] HR MS for C.sub.25H.sub.25N.sub.4O.sub.5 [M+H].sup.+ calculated 461.18195; found 461.18205.
Example 7
Methyl (S)-4-(2-oxo-2-(1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetamido)benzoate
[0166] Precursor 1g (LC-MS R.sub.t,1 4.03 min, R.sub.t,2 4.11 min, m/z 492.20 [M+Na].sup.+) was obtained from General Procedure 1. Precursor 1g was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2g (137 mg, 32% yield; LC-MS R.sub.t,1 3.42 min, R.sub.t,2 3.57 min, m/z 491.21 [M+H].sup.+). Precursor 2g was oxidized to the final α-ketoamide 3g (76 mg, 72% yield) by General Procedure 4.
[0167] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 10.98 (s, 1H, COCONH); 9.04 (t, 1H, J.sub.NH,CH2=6.0 Hz, NH-2′); 9.00 (d, 1H, J.sub.2,3=4.4 Hz, H-2); 8.30 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.08 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 8.00-7.93 (m, 4H, H-o,m-Ph); 7.82 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.4 Hz, H-7); 7.65 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.57 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 5.26 (dd, 1H, J.sub.1″,2″=8.9 and 4.7 Hz, H-1″); 4.27 (dd, 1H, J.sub.gem=16.9 Hz, J.sub.2′b,NH=5.9 Hz, H-2′b); 4.20 (dd, 1H, J.sub.gem=16.7 Hz, J.sub.2″a,NH=6.1 Hz, H-2′a); 3.83 (s, 3H, CH.sub.3COO); 3.78-3.67 (m, 2H, H-4″); 2.29 (m, 1H, H-2″b); 2.09-1.94 (m, 3H, H-3″, H-2″a);
[0168] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.08 (COCONH); 167.09 (CO-1′); 166.81 (CO-3′); 165.98 (CH.sub.3COO); 159.46 (COCONH); 150.08 (CH-2); 147.23 (C-8a); 143.14 (C-4); 142.16 (C-i-Ph); 130.51 (CH-7); 130.41 (CH-m-Ph); 128.74 (CH-8); 127.74 (CH-6); 126.15 (CH-5); 125.49 (C-p-Ph); 124.50 (C-4a); 120.32 (CH-o-Ph); 119.35 (CH-3); 60.36 (CH-1″); 52.28 (CH.sub.3COO); 46.21 (CH.sub.2-4″); 41.53 (CH.sub.2-2′); 28.16 (CH.sub.2-2″); 25.07 (CH.sub.2-3″);
[0169] LC-MS R.sub.t,1 3.60 min, R.sub.t,2 3.70 min, m/z 489.18 [M+H].sup.+;
[0170] HR MS for C.sub.26H.sub.25N.sub.4O.sub.6 [M+H].sup.+ calculated 489.17686; found 489.17664.
Example 8
(S)-N-(2-(2-(2-(Cyclopropylamino)-2-oxoacetyl)pyrrolidin-1yl)-2-oxoethyl)quinoline-4-carboxamide
[0171] Precursor 1h (1608 mg, 75% yield; LC-MS R.sub.t,1 3.51 min, R.sub.t,2 3.58 min, m/z 376.34 [M+H].sup.+) was obtained from General Procedure 1. Precursor 1h was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give precursor 2h (176 mg, 78% yield; LC-MS R.sub.t,1 2.85 min, R.sub.t,2 2.94 min, m/z 397.36 [M+H].sup.+). Precursor 2h was oxidized to the final α-ketoamide 3h (67 mg, 77% yield) by General Procedure 4.
[0172] .sup.1H NMR (500 MHz, CDCl.sub.3): 8.91 (d, 1H, J.sub.2,3=4.3 Hz, H-2); 8.26 (bd, 1H, J.sub.5,6=8.5 Hz, H-5); 8.12 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.74 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.4 Hz, H-7); 7.60 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.48 (d, 1H, J.sub.3,2=4.3 Hz, H-3); 7.14 (bt, 1H, J.sub.NH,2′=4.3 Hz, NH-2′); 7.00 (bd, 1H, J.sub.NH,CH=3.9 Hz, NH-cp); 5.33 (dd, 1H, J.sub.1″,2−=9.0 and 5.5 Hz, H-1″); 4.39 (dd, 1H, J.sub.gem=17.7 Hz, J.sub.2′b,NH=4.6 Hz, H-2′b); 4.29 (dd, 1H, J.sub.gem=17.7 Hz, J.sub.2′a,NH=4.0 Hz, H-2′a); 3.72-3.57 (m, 2H, H-4″); 2.76 (m, 1H, CH-cp); 2.39 (m, 1H, H-2″b); 2.16-1.92 (m, 3H, H-2″a, H-3″); 0.86-0.76 and 0.64-0.51 (2×m, 2×2H, CH.sub.2-cp);
[0173] .sup.13C NMR (125.7 MHz, CDCl.sub.3): 194.42 (CO-1″); 167.15 (CO-1′); 166.11 (CO-3′); 160.47 (CONH-cp); 149.73 (CH-2); 148.58 (C-8a); 141.07 (C-4); 129.99 (CH-7); 129.77 (CH-8); 127.73 (CH-6); 125.26 (CH-5); 124.36 (C-4a); 118.78 (CH-3); 60.85 (CH-1″); 46.35 (CH.sub.2-4″); 42.30 (CH.sub.2-2′);28.33 (CH.sub.2-2″); 24.93 (CH.sub.2-3″); 22.38 (CH-cp); 6.37 and 6.34 (CH2-cp);
[0174] LC-MS R.sub.t,1 2.91 min, R.sub.t,2 3.04 min, m/z 395.34 [M+H].sup.+;
[0175] HR MS for C.sub.21H.sub.23N.sub.4O.sub.4 [M+H].sup.+ calculated 395.17138; found 395.17106.
Example 9
(S)-N-(2-(2-(2-(Isopropylamino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)quinoline-4-carboxamide
[0176] Precursor 1i (225 mg, 60% yield; LC-MS R.sub.t,1 3.66 min, R.sub.t,2 3.73 min, m/z 378.38 [M+H].sup.+) was obtained from General procedure 1. Precursor 1i was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2i (80 mg, 48% yield; LC-MS R.sub.t,1 3.00 min, R.sub.t,2 3.10 min, m/z 399.36 [M+H].sup.+). Precursor 2i was oxidized to the final α-ketoamide 3i (27 mg, 39% yield) by General Procedure 4.
[0177] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.06 (m, 1H, NH-2′); 9.05 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 8.58 (bd, 1H, J.sub.NH,CH=8.2 Hz, COCONH); 8.35 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.12 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.89 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.7,6=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.73 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.64 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 5.21 (dd, 1H, J.sub.1″,2″=9.2 and 4.3 Hz, H-1″); 4.25 (dd, 1H, J.sub.gem=16.9 Hz, J.sub.2′b,NH=5.9 Hz, H-2′b); 4.17 (dd, 1H, J.sub.gem=16.9 Hz, J.sub.2′a,NH=6.0 Hz, H-2′a); 3.98-3.87 (m, 1H, (CH.sub.3).sub.2CH); 3.72-3.61 (m, 2H, H-4″); 2.23 (m, 1H, H-2″b); 2.00 (m, 1H, H-3″b); 1.91-1.77 (m, 2H, H-2″a, H-3″a); 1.11 and 1.10 (2×d, 2×3H, (CH.sub.3).sub.2CH);
[0178] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.80 (COCONH); 166.94 (CO-1′); 166.54 (CO-3′); 159.66 (COCONH); 149.82 (CH-2); 146.58 (C-8a); 143.89 (C-4); 130.92 (CH-7); 128.21 (CH-8); 128.00 (CH-6); 126.28 (CH-5); 124.61 (C-4a); 119.42 (CH-3); 60.56 (CH-1″); 46.13 (CH.sub.2-4″); 41.60 (CH.sub.2-2′); 41.02 ((CH.sub.3).sub.2CH); 27.95 (CH.sub.2-2″); 24.74 (CH.sub.2-3″); 22.07 ((CH.sub.3).sub.2CH);
[0179] LC-MS R.sub.t,1 3.11 min, R.sub.t,2 3.22 min, m/z 397.35 [M+H].sup.+;
[0180] HR MS for C.sub.21H.sub.25N.sub.4O.sub.4 [M+H].sup.+ calculated 397.18703; found 397.18665.
Example 10
(S)-N-(2-Oxo-2-(2-(2-oxo-2-(pentylamino)acetyl)pyrrolidin-1-ypethyl)quinoline-4-carboxamide
[0181] Precursor 1j was obtained from General Procedure 1 (370 mg, 90% yield; LC-MS R.sub.t,1 4.11 min, R.sub.t,2 4.17 min, m/z 406.39 [M+H].sup.+). Precursor 1j was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2j (291 mg, 64% yield; LC-MS R.sub.t,1 3.50 min, R.sub.t,2 3.61 min, m/z 427.39 [M+H].sup.+). Precursor 2j was oxidized to the final α-ketoamide 3j (98 mg, 70% yield) by General Procedure 4.
[0182] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.03 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 9.03 (m, 1H, NH-2′); 8.74 (bt, 1H, J.sub.NH,CH2=6.0 Hz, COCONH); 8.35 (bdd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.11 (bd, 1H, J.sub.8,7=8.5 Hz, H-8); 7.86 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.71 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.61 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 5.23 (bdd, 1H, J.sub.1″,2″=9.3 and 4.5 Hz, H-1″); 4.26 and 4.22 (2×dd, 2×1H, J.sub.gem=16.8 Hz, J.sub.2′,NH=6.0 Hz, H-2′); 3.70-3.62 (m, 2H, H-4″); 3.19-3.06 (m, 2H, CH.sub.2(CH.sub.2).sub.3CH.sub.3); 2.24 (m, 1H, H-2″b); 2.00 (m, 1H, H-3″b); 1.92-1.74 (m, 2H, H-3″a,2″a); 1.46 (m, 2H, CH.sub.2CH.sub.2(CH.sub.2).sub.2CH.sub.3); 1.32-1.17 (m, 4H, (CH.sub.2).sub.2CH.sub.2CH.sub.2CH.sub.3); 0.84 (t, 3H, J.sub.CH3,CH2=7.1 Hz, (CH.sub.2).sub.4CH.sub.3);
[0183] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.66 (COCONH); 166.96 (CO-1′); 166.52 (CO-3′); 160.42 (COCONH); 149.89 (CH-2); 146.81 (C-8a); 143.61 (C-4); 130.74 (CH-7); 128.39 (CH-8); 127.88 (CH-6); 126.23 (CH-5); 124.57 (C-4a); 119.38 (CH-3); 60.46 (CH-1″); 46.11 (CH.sub.2-4″); 41.57 (CH.sub.2-2′); 38.79 (CH.sub.2(CH.sub.2).sub.3CH.sub.3); 28.75 ((CH.sub.2).sub.2CH.sub.2CH.sub.2CH.sub.3); 28.58 (CH.sub.2CH.sub.2(CH.sub.2).sub.2CH.sub.3); 27.91(CH.sub.2-2″); 24.73 (CH.sub.2-3″); 22.00 ((CH.sub.2).sub.3CH.sub.2CH.sub.3); 14.12 ((CH.sub.2).sub.4CH.sub.3);
[0184] LC-MS R.sub.t,1 3.63 min, R.sub.t,2 3.76 min, m/z 425.34 [M+H].sup.+;
[0185] HR MS for C.sub.23H.sub.29N.sub.4O.sub.4 [M+H].sup.+ calculated 425.21833; found 425.21812.
Example 11
Methyl (S)-(2-oxo-2-(1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)glycinate
[0186] Precursor 1k (800 mg, 95% yield; LC-MS R.sub.t,1 3.46 min, R.sub.t,2 3.51 min, m/z 408.32 [M+H].sup.+) was obtained from General Procedure 1. Precursor 1k was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2k (500 mg, 75% yield; LC-MS R.sub.t,1 2.84 min, R.sub.t,2 2.91 min, m/z 429.30 [M+H].sup.+). Precursor 2k was oxidized to the final α-ketoamide 3k (15 mg, 46% yield) by General Procedure 4.
[0187] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.10 (bt, 1H, J.sub.NH,CH2=6.1 Hz, COCONH); 9.03 (t, 1H, J.sub.NH,2′=6.1 Hz, NH-2′); 9.02 (d, 1H, J.sub.2,3=4.4 Hz, H-2); 8.34 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.10 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.85 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.4 Hz, H-7); 7.71 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.60 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 5.22 (dd, 1H, J.sub.1″,2″=9.2 and 4.5 Hz, H-1″); 4.28 (dd, 1H, J.sub.gem=16.9 Hz, J.sub.2′b,NH=6.1 Hz, H-2′b); 4.17 (dd, 1H, J.sub.gem=16.9 Hz, J.sub.2′a,NH=6.0 Hz, H-2′a); 3.99-3.87 (m, 2H, CH.sub.3COOCH.sub.2); 3.72-3.60 (m, 2H, H-4″); 3.65 (s, 3H, CH.sub.3COOCH.sub.2); 2.25 (m, 1H, H-2″b); 2.02 (m, 1H, H-3″b); 1.88 (m, 1H, H-3″a); 1.84 (m, 1H, H-2″a);
[0188] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 194.92 (COCONH). 169.62 (CH.sub.3COO); 167.05 (CO-1′); 166.63 (CO-3′); 160.80 (COCONH); 150.02 (CH-2); 147.12 (C-8a); 143.31 (C-4); 130.58 (CH-7); 128.63 (CH-8); 127.82 (CH-6); 126.19 (CH-5); 124.53 (C-4a); 119.37 (CH-3); 60.52 (CH-1″); 52.18 (CH.sub.3COO); 46.10 (CH.sub.2-4″); 41.57 (CH.sub.2-2′); 40.78 (CH3COOCH2); 27.79 (CH.sub.2-2″); 24.72 (CH2-3″);
[0189] LC-MS R.sub.t,1 2.90 min, R.sub.t,2 3.00 min, m/z 427.29 [M+H].sup.+;
[0190] HR MS for C.sub.21H.sub.23N.sub.4O.sub.6 [M+H].sup.+ calculated 427.16121; found 427.16096.
Example 12
terc-Butyl (S)-(2-oxo-2-(1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)glycinate
[0191] Precursor 11 (212 mg, 46% yield; LC-MS R.sub.t,1 3.51 min, R.sub.t,2 3.57 min, m/z 472.28 [M+Na].sup.+) was obtained from General Procedure 1. Precursor 11 was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 21 (140 mg, 62% yield; LC-MS R.sub.t,1 3.40 min, R.sub.t,2 3.48 min, m/z 471.30 [M+H].sup.+). Precursor 21 was oxidized to the final α-ketoamide 3l (55 mg, 50% yield) by General Procedure 4.
[0192] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.07 (m, 1H, NH-2′); 9.06 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 9.00 (bt, 1H, J.sub.NH,CH2=6.2 Hz, COCONH); 8.37 (bdd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.12 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.88 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.74 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.65 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 5.23 (dd, 1H, J.sub.1″,2″=9.2 and 4.3 Hz, H-1″); 4.29 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′b,NH=6.1 Hz, H-2′b); 4.17 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.9 Hz, H-2′a); 3.86-3.74 (m, 2H, CH.sub.2COO); 3.72-3.62 (m, 2H, H-4″); 2.26 (m, 1H, H-2″b); 2.02 (m, 1H, H-3″b); 1.92-1.78 (m, 2H, H-3″a,2″a); 1.41 (s, 9H, (CH.sub.3).sub.3C);
[0193] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.02 (COCONH). 168.18 (CH.sub.2COO); 166.90 (CO-1′); 166.59 (CO-3′); 160.76 (COCONH); 149.67 (CH-2); 146.27 (C-8a); 144.14 (C-4); 131.05 (CH-7); 128.13 (CH-6); 127.95 (CH-8); 126.32 (CH-5); 124.65 (C-4a); 119.46 (CH-3); 81.31 ((CH.sub.3).sub.3C); 60.52 (CH-1″); 46.12 (CH.sub.2-4″); 41.61 (CH.sub.2-2′); 41.52 (CH.sub.2COO); 27.92 ((CH.sub.3).sub.3C); 27.83 (CH.sub.2-2″); 24.71 (CH.sub.2-3′');
[0194] LC-MS R.sub.t,1 3.53 min, R.sub.t,2 3.62 min, m/z 469.29 [M+H].sup.+;
[0195] HR MS for C.sub.24H.sub.29N.sub.4O.sub.6 [M+H].sup.+ calculated 469.20816; found 469.20798.
Example 13
Methyl (2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)alaninate
[0196] General Procedure 1 gave precursor 1ma ((2-((S)-1-(((benzyloxy)carbonyl)glycyl)pyrrolidin-2-yl)-2-hydroxyacetyl)alanine; 237 mg, 82% yield; LC-MS R.sub.t,1 3.24 min, R.sub.t,2 3.34 min, m/z 408.27 [M+H].sup.+), which was converted to the methyl ester by an esterification corresponding to General Procedure 3 using an excess of methanol instead of an amine (Precursor 1m; 100 mg, 44% yield; LC-MS R.sub.t,1 3.60 min, R.sub.t,2 3.66 min, m/z 422.36 [M+H].sup.+). Precursor 1m was subsequently debenzylated by General Procedure 2, and the resulting amine was condensed with quinoline-4-carboxylic acid by General Procedure 3 to give Precursor 2m (76 mg, 58% yield; LC-MS R.sub.t,1 2.95 min, R.sub.t,2 3.03 min, R.sub.t,2 3.05 min, m/z 443.28 [M+H].sup.+). Precursor 2m was oxidized to the final α-ketoamide 3m (49 mg, 87% yield) by General Procedure 4.
[0197] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.13 and 9.12 (2×bd, 2×1H, J.sub.NH,CH=7.5 Hz, COCONH); 9.06 (m, 2H, NH-2′); 9.06 (2×d, 2×1H, J.sub.2,3=4.5 Hz, H-2); 8.38 and 8.36 (2×dm, 2×1H, J.sub.5,6=8.6 Hz, H-5); 8.12 (2×dm, 2×1H, J.sub.8,7=8.5 Hz, H-8); 7.89 and 7.88 (2×ddd, 2×1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.75 and 7.73 (2×ddd, 2×1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.65 and 7.64 (2×bd, 2×1H, J.sub.3,2=4.5 Hz, H-3); 5.24 (dd, 1H, J.sub.1,2=9.2 and 4.5 Hz, H-1″); 5.20 (dd, 1H, J.sub.1″,2″=9.3 and 4.2 Hz, H-1″); 4.40 and 4.39 (2×pent, 2×1H, J.sub.CH,NH=J.sub.CH,CH3=7.4 Hz, CH.sub.3CH); 4.28 and 4.27 (2×dd, 2×1H, J.sub.gem=16.8 Hz, J.sub.2′b,NH=6.0 Hz, H-2′b); 4.19 (2×dd, 2×1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.9 Hz, H-2′a); 3.75-3.60 (2×m, 2×2H, H-4″); 3.64 (2×s, 2×3H, CH.sub.3COO); 2.30-2.20 (m, 2×1H, H-2″b); 2.06-1.96 (m, 2×1H, H-3″b); 1.93-1.77 (m, 4×1H, H-3″a, H-2″a); 1.36 and 1.34 (2×d, 2×3H, J.sub.CH3,CH=7.3 Hz, CH.sub.3CH);
[0198] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.25 and 195.17 (COCONH); 172.49 (CH.sub.3COO); 167.10 (CO-1′); 166.86 and 166.79 (CO-3′); 160.85 and 160.48 (COCONH); 149.90 and 149.88 (CH-2); 146.54 and 146.50 (C-8a); 144.39 and 144.29 (C-4); 131.27 and 131.24 (CH-7); 128.32 and 128.29 (CH-6); 128.22 and 128.16 (CH-8); 126.55 and 126.50 (CH-5); 124.86 and 124.85 (C-4a); 119.66 (CH-3); 61.10 and 60.62 (CH-1″); 52.59 and 52.56 (CH.sub.3COO); 48.10 and 48.04 (CH.sub.3CH); 46.32 (CH.sub.2-4″); 41.84 and 41.80 (CH.sub.2-2′); 28.03 and 27.96 (CH.sub.2-2″); 24.94 and 24.88 (CH.sub.2-3″); 16.95 and 16.84 (CH.sub.3CH);
[0199] LC-MS R.sub.t,1 3.07 min, R.sub.t,2 3.15 min, m/z 441.25[M+H].sup.+;
Example 14
(S)-N-(2-(2-(2-((2-(Dimethylamino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)quinoline-4-carboxamide
[0200] In successive General Procedures 3 and 4, α-ketoamide 5a (29 mg, 69% yield) was prepared from Precursor 7 and an ethanolic solution of dimethylamine (5.6 mol.Math.l.sup.−1).
[0201] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.04 (m, 1H, NH-2′); 9.02 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 8.50 (bt, 1H, J.sub.NH,CH2=5.5 Hz, COCONH); 8.34 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.10 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.85 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.71 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.4,7=6.9 Hz, J.sub.4,8=1.3 Hz, H-6); 7.61 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 5.24 (dd, 1H, J.sub.1″,2″=9.2 and 4.2 Hz, H-1″); 4.29 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′b,NH=6.2 Hz, H-2′b); 4.16 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.8 Hz, H-2′a); 4.03 and 3.98 (2×dd, 2×1H, J.sub.gem=17.0 Hz, J.sub.CH2,NH=5.7 Hz; CH.sub.2CON); 3.72-3.61 (m, 2H, H-4″); 2.96 and 2.83 (2×s, 2×3H, (CH.sub.3).sub.2N); 2.25 (m, 1H, H-2″b); 2.02 (m, 1H, H-3″b); 1.93-1.81 (m, 2H, H-3″a,2″a);
[0202] .sup.13C NMR (125.7 MHz, DMSO-d6): 195.18 (COCONH). 167.25 (CH.sub.2CON); 167.05 (CO-1′); 166.64 (CO-3′); 160.26 (COCONH); 149.98 (CH-2); 146.99 (C-8a); 143.45 (C-4); 130.68 (CH-7); 128.53 (CH-8); 127.90 (CH-6); 126.22 (CH-5); 124.56 (C-4a); 119.41 (CH-3); 60.46 (CH-1″); 46.13 (CH.sub.2-4″); 41.59 (CH.sub.2-2′); 40.68 (CH.sub.2CON); 35.86 and 35.34 ((CH.sub.3).sub.2N); 27.77 (CH.sub.2-2″); 24.72 (CH.sub.2-3″);
[0203] LC-MS R.sub.t,1 2.79 min, R.sub.t,2 2.88 min, m/z 440.26 [M+H].sup.+;
[0204] HR MS for C.sub.22H.sub.26N.sub.5O.sub.5 [M+H].sup.+ calculated 440.19285; found 440.19275.
Example 15
(S)-N-(2-(2-(2-((2-(Ethyl(propyl)amino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)quinoline-4-carboxamide
[0205] In successive General Procedures 3 and 4, α-ketoamide 5b (18 mg, 50% yield) was prepared from Precursor 7 and pyrrolidine.
[0206] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.02 (m, 1H, NH-2′); 9.00 (d, 1H, J.sub.2,3=4.4 Hz, H-2); 8.56 (bt, 1H, J.sub.NH,CH2=5.7 Hz, COCONH); 8.33 (bdd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.09 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.84 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.70 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.58 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 5.23 (dd, 1H, J.sub.1″,2″=9.2 and 4.3 Hz, H-1″); 4.28 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′b,NH=6.1 Hz, H-2′b); 4.15 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.8 Hz, H-2′a); 3.98-3.87 (m, 2H, CH.sub.2CONH); 3.72-3.62 (m, 2H, H-4″); 3.41 and 3.29 (2×t, 2×2H, J.sub.CH2,CH2=6.9 Hz; CH.sub.2-2,5-C.sub.4H.sub.8N); 2.24 (m, 1H, H-2″b); 2.01 (m, 1H, H-3″b); 1.92-1.71 (m, 6H, H-3″a,2″a, H-3,4-C.sub.4H.sub.8N);
[0207] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.21 (COCONH), 167.14 (CO-1′); 166.66 (CO-3′); 165.62 (CH.sub.2CONH); 160.35 (COCONH); 150.17 (CH-2); 147.39 (C-8a); 143.06 (C-4); 130.47 (CH-7); 128.86 (CH-8); 127.77 (CH-6); 126.17 (CH-5); 124.51 (C-4a); 119.38 (CH-3); 60.52 (CH-1″); 46.14 (CH.sub.2-4″); 45.89 and 45.15 (CH.sub.2-2,5-C.sub.4H.sub.8N); 41.59 (CH.sub.2-2′); 41.41 (CH.sub.2CON); 27.78 (CH.sub.2-2″); 25.81 (CH.sub.2-3-C.sub.4H.sub.8N or CH.sub.2-4-C.sub.4H.sub.8N); 24.73 (CH.sub.2-3″); 23.94 81 (CH.sub.2-3-C.sub.4H.sub.8N or CH.sub.2-4-C.sub.4H.sub.8N);
[0208] LC-MS R.sub.t,1 2.98 min, R.sub.t,2 3.03 min, m/z 466.26 [M+H].sup.+;
Example 16
(S)-N-(2-(2-(2-((2-(Isopropylamino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)quinoline-4-carboxamide
[0209] In successive General Procedures 3 and 4, α-ketoamide 5c (21 mg, 66% yield) was prepared from Precursor 7 and isopropylamine.
[0210] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.02 (t, 1H, J.sub.NH,2′=6.0 Hz, NH-2′); 9.00 (d, 1H, J.sub.2,3=4.4 Hz, H-2); 8.67 (t, 1H, J.sub.NH,CH2=6.0 Hz, COCONH); 8.33 (ddd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, J.sub.5,8=0.6 Hz, H-5); 8.09 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.84 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.83 (m, 1H, (CH.sub.3).sub.2CHNH); 7.69 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.58 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 5.23 (dd, 1H, J.sub.1″,2″=9.2 and 4.2 Hz, H-1″); 4.28 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′b,NH=6.1 Hz, H-2′b); 4.17 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.9 Hz, H-2′a); 3.81 (m, 1H, (CH.sub.3).sub.2CHNH); 3.76-3.62 (m, 4H, CH.sub.2CONH, H-4″); 2.23 (m, 1H, H-2″b); 2.01 (m, 1H, H-3″b); 1.90 -1.83 (m, 2H, H-3″a,2″a); 1.04 and 1.03 (2×d, 2×3H, J.sub.CH3,CH=6.6 Hz, (CH.sub.3).sub.2CHNH);
[0211] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 195.05 (COCONH), 167.13 (CO-1′); 166.72 and 166.62 (CO-3′, CH.sub.2CONH); 160.47 (COCONH); 150.16 (CH-2); 147.44 (C-8a); 143.01 (C-4); 130.42 (CH-7); 128.89 (CH-8); 127.73 (CH-6); 126.17 (CH-5); 124.50 (C-4a); 119.35 (CH-3); 60.40 (CH-1″); 46.12 (CH.sub.2-4″); 41.94 (CH.sub.2CONH); 41.57 (CH.sub.2-2′); 40.81 ((CH.sub.3).sub.2CH); 27.75 (CH.sub.2-2″); 24.72 (CH.sub.2-3″); 22.58 ((CH.sub.3).sub.2CH);
[0212] LC-MS R.sub.t,1 3.05 min, R.sub.t,2 3.11 min, m/z 454.24 [M+H].sup.+;
[0213] HR MS for C.sub.23H.sub.27N.sub.5O.sub.5 [M+H].sup.+ calculated 454.20850; found 454.20844.
Example 17
(S)-N-(2-(2-(2-((2-(Benzylamino)-2-oxoethyl)amino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)quinoline-4-carboxamide
[0214] In successive General Procedures 3 and 4, α-ketoamide 5d (10 mg, 19% yield) was prepared from Precursor 7 and benzylamine.
[0215] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.01 (m, 1H, NH-2′); 8.99 (d, 1H, J.sub.2,3=4.4 Hz, H-2); 8.85 (bt, 1H, J.sub.NH,CH2=6.0 Hz, COCONH); 8.48 (bt, 1H, J.sub.NH,CH2=6.0 Hz, NH—CH.sub.2Bn); 8.33 (bdd, 1H, J.sub.5,6=8.5 Hz, J.sub.5,7=1.5 Hz, H-5); 8.09 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.83 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.69 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.57 (d, 1H, J.sub.3,2=4.4 Hz, H-3); 7.31 (m, 2H, H-m-Bn); 7.27-7.20 (m, 3H, H-o,p-Bn); 5.25 (dd, 1H, J.sub.1″,2″=9.2 and 4.2 Hz, H-1″); 4.28 (m, 2H, CH.sub.2-Bn); 4.27 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2°b,NH=6.0 Hz, H-2′b); 4.16 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.9 Hz, H-2′a); 3.86 (dd, 1H, J.sub.gem=16.4 Hz, J.sub.CH2,NH=6.3 Hz, CH.sub.2CONH-b); 3.78 (dd, 1H, J.sub.gem=16.4 Hz, J.sub.CH2,NH=6.0 Hz, CH.sub.2CONH-a); 3.71-3.62 (m, 2H, H-4″); 2.24 (m, 1H, H-2″b); 2.01 (m, 1H, H-3″b); 1.94-1.84 (m, 2H, H-3″a,2″a);
[0216] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 194.85 (COCONH); 168.01 (CH.sub.2CONH); 167.13 (CO-1′); 166.62 (CO-3′); 160.56 (COCONH); 150.19 (CH-2); 147.49 (C-8a); 142.97 (C-4); 139.44 (C-i-Bn); 130.39 (CH-7); 128.94 (CH-8); 128.49 (CH-m-Bn); 127.70 (CH-6); 127.40 (CH-o-Bn); 127.02 (CH-p-Bn); 126.14 (CH-5); 124.49 (C-4a); 119.33 (CH-3); 60.44 (CH-1″); 46.11 (CH.sub.2-4″); 42.28 (CH.sub.2-Bn); 41.19 (CH.sub.2CONH); 41.57 (CH.sub.2-2′); 27.70 (CH.sub.2-2″); 24.70 (CH.sub.2-3″);
[0217] LC-MS R.sub.t,1 3.26 min, R.sub.t,2 3.35 min, m/z 502.21 [M+H].sup.+;
[0218] HR MS for C.sub.27H.sub.28N.sub.5O.sub.5 [M+H].sup.+ calculated 502.20850; found 502.20825.
Example 18
Methyl(2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)glycyl-L-leucinate
[0219] In successive General Procedures 3 and 4, α-ketoamide 5e (33 mg, 77% yield) was prepared from Precursor 7 and methyl-L-leucinate.
[0220] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.05 (m, 1H, NH-2′); 9.05 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 8.77 (bt, 1H, J.sub.NH,CH2=6.2 Hz, COCONH); 8.40 (bd, 1H, J.sub.NH,CH=7.9 Hz, CH.sub.3COOCHNH); 8.36 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.12 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.87 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.74 (ddd, 1H, J.sub.6,5=8.4 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.64 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 5.25 (dd, 1H, J.sub.1″,2″=9.3 and 4.0 Hz, H-1″); 4.31 (m, 1H, CH.sub.3COOCHNH); 4.28 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′b,NH=6.1 Hz, H-2′b); 4.17 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.8 Hz, H-2′a); 3.86-3.75 (m, 2H, CH.sub.2CONH); 3.72-3.62 (m, 2H, H-4″); 3.62 (s, 3H, CH.sub.3COOCH); 2.23 (m, 1H, H-2″b); 2.01 (m, 1H, H-3″b); 1.92-1.83 (m, 2H, H-3″a,2″a); 1.60 (m, 1H, CH.sub.2CH(CH.sub.3).sub.2); 1.55 and 1.48 (2×m, 2×1H, CH.sub.2CH(CH.sub.3).sub.2); 0.87 and 0.83 (2×d, 2×3H, J.sub.CH3,CH=6.5 Hz, CH.sub.2CH(CH.sub.3).sub.2);
[0221] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 194.80 (COCONH); 173.16 (CH.sub.3COOCH); 168.13 (CH.sub.2CONH); 166.92 (CO-1′); 166.57 (CO-3′); 160.48 (COCONH); 149.74 (CH-2); 146.46 (C-8a); 143.96 (C-4); 130.93 (CH-7); 128.06 (CH-6); 128.00 (CH-8); 126.28 (CH-5); 124.62 (C-4a); 119.43 (CH-3); 60.47 (CH-1″); 52.14 (CH.sub.3COOCH); 50.45 (CH.sub.3COOCH); 46.12 (CH.sub.2-4″); 41.75 (CH.sub.2CONH); 41.60 (CH.sub.2-2′); 40.12 (CH.sub.2CH(CH.sub.3).sub.2); 27.64 (CH.sub.2-2″); 24.65 (CH.sub.2-3″), 24.35 (CH.sub.2CH(CH.sub.3).sub.2); 22.98 and 21.49 (CH.sub.2CH(CH.sub.3).sub.2);
[0222] LC-MS R.sub.t,1 3.46 min, R.sub.t,2 3.52 min, m/z 540.26 [M+H].sup.+;
[0223] HR MS for C.sub.27H.sub.34N.sub.5O.sub.7 [M+H].sup.+ calculated 540.24527; found 540.24499.
Example 19
Methyl(2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)glycyl-L-phenylalaninate
[0224] In successive General Procedures 3 and 4, α-ketoamide 5f (45 mg, 79% yield) was prepared from Precursor 7 and methyl-L-phenylalaninate.
[0225] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.04 (m, 1H, NH-2′); 9.04 (d, 1H, J.sub.2,3=4,5 Hz, H-2); 8.74 (bt, 1H, J.sub.NH,CH2=6.2 Hz, COCONH); 8.50 (bd, 1H, J.sub.NH,CH=7.7 Hz, CH.sub.3COOCHNH); 8.35 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.11 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.87 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1.5 Hz, H-7); 7.73 (ddd, 1H, J.sub.6,5=8.5 Hz, J.sub.6,7=6.9 Hz, J.sub.6,8=1.3 Hz, H-6); 7.63 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 7.27 (m, 2H, H-m-Bn); 7.23-7.18 (m, 3H, H-o,p-Bn); 5.24 (dd, 1H, J.sub.1″,2″=9.2 and 4.1 Hz, H-1″); 4.47 (m, 1H, CH.sub.3COOCH); 4.28 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.240 b,NH=6.1 Hz, H-2′b); 4.17 (dd, 1H, J.sub.gem=16.8 Hz, J.sub.2′a,NH=5.9 Hz, H-2′a); 3.82 (dd, 1H, J.sub.gem=16.6 Hz, J.sub.CH2,NH=6.3 Hz, CH.sub.2CONH-b); 3.72 (dd, 1H, J.sub.gem=16.6 Hz, J.sub.CH2,NH=6.1 Hz, CH.sub.2CONH-a); 3.71-3.61 (m, 2H, H-4″); 3.60 (s, 3H, CH.sub.3COO); 3.02 (dd, 1H, J.sub.gem=13.7 Hz, J.sub.CH2,CH=5.7 Hz, CH.sub.2-Bn-b); 2.91 (dd, 1H, J.sub.gem=13.7 Hz, J.sub.CH2,CH=9.0 Hz, CH.sub.2-Bn-a); 2.24 (m, 1H, H-2″b); 2.01 (m, 1H, H-3″b); 1.90-1.82 (m, 2H, H-3″a,2″a);
[0226] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 194.88 (COCONH); 172.09 (CH.sub.3COO); 168.08 (CH.sub.2CONH); 166.92 (CO-1′); 166.56 (CO-3′); 160.41 (COCONH); 149.75 (CH-2); 146.50 (C-8a); 143.89 (C-4); 137.21 (C-i-Bn); 130.90 (CH-7); 129.34 (CH-o-Bn); 128.53 (CH-m-Bn); 128.13 (CH-8); 128.03 (CH-6); 126.86 (CH-p-Bn); 126.27 (CH-5); 124.60 (C-4a); 119.42 (CH-3); 60.44 (CH-1″); 53.94 (CH.sub.3COOCH); 52.16 (CH.sub.3COO); 46.10 (CH.sub.2-4″); 41.67 (CH.sub.2CONH); 41.59 (CH.sub.2-2′); 36.85 (CH.sub.2-Bn); 27.70 (CH.sub.2-2″); 24.68 (CH.sub.2-3″);
[0227] LC-MS R.sub.t,1 3.52 min, R.sub.t,2 3.59 min, m/z 574.28 [M+H].sup.+;
[0228] HR MS for C.sub.30H.sub.32N.sub.5O.sub.7 [M+H].sup.+ calculated 574.22962; found 574.22949.
Example 20
Methyl(2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)glycyl-L-glutaminate
[0229] In successive General Procedures 3 and 4, α-ketoamide 5g (13 mg, 47% yield; LC-MS R.sub.t,1 2.69 min, R.sub.t,2 2.78 min, m/z 555.25 [M+H].sup.+) was prepared from Precursor 7 and methyl-L-glutaminate.
Example 21
5-Benzyl 1-methyl (2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)glycyl-L-glutamate
[0230] In successive General Procedures 3 and 4, α-ketoamide 5h (5 mg, 43% yield; LC-MS R.sub.t,1 3.68 min, R.sub.t,2 3.78 min, m/z 646.28 [M+H].sup.+) was prepared from Precursor 7 and 5-benzyl-1-methyl-L-glutamate.
Example 22
Benzyl N.SUP.6.-((benzyloxy)carbonyl)-N.SUP.2.-((2-oxo-2-((S)-1-((quinoline-4-carbonyl)glycyl)pyrrolidin-2-yl)acetyl)glycyl)-L-lysinate
[0231] In successive General Procedures 3 and 4, α-ketoamide 5i (15 mg, 60% yield) was prepared from Precursor 7 and methyl N6-Cbz-L-lysinate.
[0232] .sup.1H NMR (500 MHz, DMSO-d.sub.6): 9.02 (m, 1H, NH-2′); 9.01 (d, 1H, J.sub.2,3=4.5 Hz, H-2); 8.76 (bt, 1H, J.sub.NH,CH2=6.2 Hz, COCONH); 8.39 (bd, 1H, J.sub.NH,CH=7.5 Hz, CH.sub.3COOCHNH); 8.33 (dm, 1H, J.sub.5,6=8.5 Hz, H-5); 8.09 (dm, 1H, J.sub.8,7=8.5 Hz, H-8); 7.84 (ddd, 1H, J.sub.7,8=8.5 Hz, J.sub.8,7=6.9 Hz, J.sub.7,5=1,5 Hz, H-7); 7.70 (m, 1H, H-6); 7.59 (d, 1H, J.sub.3,2=4.5 Hz, H-3); 7.39-7.27 (m, 5H, H-o,m,p-Ph); 7.26 (m, 1H, NH-5′″); 5.24 (dd, 1H, J.sub.1″,2″=9.2 and 4.0 Hz, H-1″); 5.00 (s, 2H, COOCH.sub.2Ph); 4.28 (dd, 1H, J.sub.gem=16.9 Hz, J.sub.2′b,NH=6.1 Hz, H-2′b); 4.22 (m, 1H, CH-1′″); 4.16 (dd, 1H, J.sub.gem=16.9 Hz, J.sub.2′a,NH=6.0 Hz, H-2′a); 3.86-3.76 (m, 2H, CH.sub.2CONH); 3.70-3.61 (m, 2H, H-4″); 3.62 (s, 3H, CH.sub.3COO); 2.97 (m, 2H, H-5′″); 2.22 (m, 1H, H-2″b); 2.00 (m, 1H, H-3″b); 1.92-1.83 (m, 2H, H-3″a,2″a); 1.59 (m, 2H, CH.sub.2-2′″); 1.38 (m, 2H, CH.sub.2-4′″); 1.26 (m, 2H, CH.sub.2-3′″);
[0233] .sup.13C NMR (125.7 MHz, DMSO-d.sub.6): 194.84 (COCONH); 172.74 (CH.sub.3COO); 168.12 (CH.sub.2CONH); 167.05 (CO-1′); 166.57 (CO-3′); 160.46 (COCONH); 156.30 (COOCH.sub.2Ph); 150.07 (CH-2); 147.17 (C-8a); 143.25 (C-4); 137.48 (C-i-Ph); 130.53 (CH-7); 128.67 (CH-8); 128.57 (CH-m-Ph); 127.97 (CH-o,p-Ph); 127.79 (CH-6); 126.18 (CH-5); 124.51 (C-4a); 119.34 (CH-3); 65.33 (COOCH.sub.2Ph); 60.43 (CH-1″); 52.12 and 52.09 (CH.sub.3COO, CH-1′″); 46.09 (CH.sub.2-4″); 41.71 (CH.sub.2CONH); 41.57 (CH.sub.2-2′); 40.25 (CH.sub.2-5′″); 30.82 (CH.sub.2-2′″); 29.14 (CH.sub.2-4′″); 27.65 (CH.sub.2-2″); 24.65 (CH.sub.2-3″), 22.75 (CH.sub.2-3′″);
[0234] LC-MS R.sub.t,1 3.72 min, R.sub.t,2 3.79 min, m/z 689.29 [M+H].sup.+;
[0235] HR MS for C.sub.35H.sub.41N.sub.6O.sub.9 [M+H].sup.+ calculated 689.29295; found 689.29276.
Example 23
(S)-S-(62-((4-((2-(2-(2-((3,4-dimethoxybenzyl)amino)-2-oxoacetyl)pyrrolidin-1yl)-2-oxoethyl)carbamoyl)quinoline-7-yl)oxy)-2,5,8,11,61-pentaoxo-15,18,21,24,27,30,33,36,39,42,45,48,51,54,57-pentadecaoxa-3,6,9,12,60-pentaazadohexacontyl) ethanthioate
[0236] Precursor 1b was debenzylated by General Procedure 2, and the resulting amine was condensed by General Procedure 3 with quinoline-4-carboxylic acid derivative 10 to give Precursor 11 (417 mg, 65% yield; LC-MS R.sub.t,1 3.76 min, R.sub.t,2 3.82 min, m/z 642.59 [½(M−COOtBu)+H].sup.+). Precursor 11 was oxidized to α-ketoamide (229 mg, 55% yield; LC-MS R.sub.t,1 3.81 min, R.sub.t,2 3.87 min, m/z 641.57 [½(M−COOtBu)+H].sup.+) by General Procedure 4. The product was then deprotected in 10 ml of 30% TFA in DCM. The liquid components were evaporated under reduced pressure, and the resulting amine was isolated by FLASH chromatography. After lyophilization of the product-containing fractions, this amine was condensed by General Procedure 3 with Boc-Gly-Gly-Gly (41 mg, 22% yield; LC-MS R.sub.t,1 3.51 min, R.sub.t,2 3.57 min, m/z 727.06 [½(M−COOtBu)+H].sup.+). The deprotection step under TFA/DCM conditions mentioned above was repeated, and the resulting amine was condensed by General Procedure 3 with S-acetyl-2-thioacetic acid to give the final Product 12. (2.2 mg, 28% yield; LC-MS R.sub.t,1 3.42 min, R.sub.t,2 3.47 min, m/z 785.10 [½M+H].sup.+).
Example 24
(S)-N-(2-(2-(2-((3,4-dimethoxybenzyl)amino)-2-oxoacetyl)pyrrolidin-1-yl)-2-oxoethyl)-7-(2-(6-hydrazinylnicotinamido)ethoxy)quinoline-4-carboxamide
[0237] Precursor 1b was debenzylated by General Procedure 2 and the resulting amine was condensed by General Procedure 3 with quinoline-4-carboxylic acid derivative 13 to give Precursor 14 (170 mg, 46% yield; LC-MS R.sub.t,1 3.61 min, R.sub.t,2 3.68 min, m/z 666.30 [M+H].sup.+). Precursor 14 was oxidized to α-ketoamide (121 mg, 72% yield; LC-MS R.sub.t,1 3.71 min, R.sub.t,2 3.78 min, m/z 664.26 [M+H].sup.+) by General Procedure 4. The product was then deprotected in 7 ml of 30% TFA in DCM. The liquid components were evaporated under reduced pressure, and the resulting amine was isolated by FLASH chromatography. After lyophilization of the product-containing fractions, this amine was condensed by General Procedure 3 with N-Boc-hydrazinonicotinic acid (24 mg, 59% yield; LC-MS R.sub.t,1 3.41 min, R.sub.t,2 3.48 min, m/z 799.31 [M+H].sup.+). The deprotection step under TFA/DCM conditions mentioned above was repeated to give the final Product 15 (1 mg, 8% yield; LC-MS R.sub.t,1 2.88 min, R.sub.t,2 2.96 min, m/z 699.20 [M+H].sup.+).
Example 25
Measuring the Inhibitory Activity of α-Ketoamide Inhibitors
[0238] The human recombinant FAP enzyme was prepared according to a previously published procedure (Dvor̆áková et al. 2017, J Med. Chem., 8365). The human recombinant enzymes DPPIV and PREP were purchased from R&D Systems (cat. numbers 9168-SE-010 and 4308-SE-010). IC.sub.50 values were measured in duplicate according to a previously published procedure (Dvor̆áková et al. 2017, J. Med. Chem., 8365). Data were analysed by nonlinear regression with GraphPrism (version 8.3.1). The measurement results are given as values of the mean inhibitory concentration IC.sub.50 and its linearized form via the negative decimal logarithm of pIC.sub.50. The most active substances exhibit the lowest IC.sub.50 and pIC.sub.50 values.
[0239] Results of Measuring the Inhibitory Activities of Substances Against FAP
TABLE-US-00002 95% confidence interval IC.sub.50 pIC.sub.50 IC.sub.50 [nmol .Math. l.sup.−1] Example Compound [mol .Math. l.sup.−1] [nmol .Math. l.sup.−1] Min Max 1 3a 8.27 ± 0.04 5.336 4.488 6.437 2 3b 9.72 ± 0.03 0.1909 0.165 0.2205 3 3c 8.36 ± 0.04 4.41 3.636 5.378 4 3d 8.34 ± 0.02 4.605 4.121 5.170 5 3e 8.84 ± 0.03 1.459 1.232 1.730 6 3f.sup. 8.17 ± 0.04 6.814 5.632 8.691 7 3g 8.50 ± 0.02 3.157 2.821 3.541 8 3h 8.37 ± 0.03 4.255 3.683 4.945 9 3i 7.68 ± 0.02 20.75 18.44 23.46 10 3j 8.53 ± 0.03 2.988 2.539 3.534 11 3k 8.10 ± 0.05 7.932 6.373 10.68 12 3l 9.57 ± 0.02 0.2676 0.2445 0.2952 13 3m 8.53 ± 0.02 2.97 2.712 3.255 14 5a 7.81 ± 0.03 15.6 13.75 17.92 15 5b 8.14 ± 0.03 7.246 6.234 8.468 16 5c 8.04 ± 0.03 9.08 7.738 10.75 17 5d 8.39 ± 0.03 4.053 3.374 4.885 18 5e 7.49 ± 0.04 32.74 27.41 39.39 19 5f.sup. 8.56 ± 0.03 2.778 2.395 3.234 20 5g 7.74 ± 0.03 18.42 15.55 21.99 21 5h 9.23 ± 0.05 0.5895 0.4548 0.7803 22 5i 8.70 ± 0.04 1.986 1.588 2.567
[0240] Results of Measurement of Inhibitory Activities of Reference Substances According to Formulas A and B Against FAP, DPPIV and PREP
TABLE-US-00003 Substance according to pIC.sub.50 FAP.sup.a DPPIV.sup.a PREP.sup.a the formula [mol .Math. l.sup.−1] IC.sub.50 [nmol .Math. l.sup.−1] A 7.55 ± 0.05 28.53 >4000 660 B 8.37 ± 0.01 4.273 >4000 670
[0241] Results of Measurement of Inhibitory Activities of Selected Substances Against DPPIV and PREP
TABLE-US-00004 FAP/PREP selectivity DPPIV PREP index Calculted as Example Compound IC.sub.50 [nmol .Math. l.sup.−1] IC.sub.50 (PREP)/IC.sub.50 (FAP) 2 3b >4000 0.4 2.1 5 .sup. 3e >4000 0.5 0.34 10 3j >4000 0.4 0.13 12 3l >4000 0.6 2.2 19 5f >4000 0.3 0.0092 22 5i >4000 0.26 0.54
Example 26
[0242] Measurement of Stability of α-Ketoamide Inhibitors
[0243] Stability in Plasma
[0244] A 10 mmol.Math.l.sup.−1 solution in DMSO was prepared from each test substance, 0.7 μl of the solution was added to 1400 μl of human (Biowest) or murine (Biosera) plasma maintained at 37° C., After 0, 20, 60 and 120 minutes, 40 μl aliquots were taken and analysed by LC-MS:
[0245] An aliquot of plasma was extracted with 120 μl of methanol containing caffeine as an internal standard. The solution was vortexed (5 min) and centrifuged (20500 g; 10 min), the supernatant was transferred to a vial, and 1 μl of the mixture was used for LC-MS analysis.
[0246] Stability in Microsomes
[0247] Murine microsomes (Thermofisher) 0.5 mg/ml were incubated with 5 μmol.Math.l.sup.−1 solution of test substance, freshly prepared 2 mmol.Math.l.sup.−1 solution of NADPH and 2 mmol.Math.l.sup.−1 MgCl.sub.2 in 90 mmol.Math.l.sup.−1 Tris buffer (pH 7.4). The incubation of 37.5 μl of the mixture was terminated by the addition of 150 μl of acetonitrile containing caffeine as an internal standard, cooled to 0° C. The mixture was vortexed (5 min) and centrifuged (20500 g; 10 min). The supernatant was transferred to a vial, and 1 μl of the mixture was used for LC-MS analysis.
[0248] LC-MS Analysis of Samples
[0249] Samples were analyzed in a Sciex Qtrap 6550 instrument and a Phenomex column was used for the separation (50×2.1, 13 nm, 1.7 μm), a flow rate of 0.3 ml/min, and a gradient with a mobile phase fraction of B (0.1% (vol./vol.) formic acid in acetonitrile) continuously increased over 6 minutes from 5 to 100% (vol./vol.) in mobile phase A (0.1% (vol./vol.) formic acid in water). Results are presented as the percentage of test substance versus control (aliquot taken at time 0).
[0250] Measurement Results:
[0251] Stability was tested for selected inhibitors 3a, 3b, 3e, 5f and 5h.
[0252] These substances are stable in human plasma. The highest rate of degradation was observed for substance 5f, where 25% of the substance degraded within 120 minutes. In murine plasma, only substances 3a, 3b and 3e are stable, while substances 5f and 5h degrade immediately (100% of the substance degraded within 20 minutes). In murine microsomes, substances 3a and 3b are stable (a maximum of 20% of the substance degraded within 120 minutes), substances 3e and 5f are partially stable (40-50% of the substance degraded within 120 minutes) and substance 5h is unstable (100% of the substance degraded within 20 minutes).
Example 27
[0253] Measurement of Cytotoxicity of α-Ketoamide Inhibitors on Tumour Cell Lines
[0254] The cytotoxicity of the substances was measured on four tumour cell lines: CCRF-CEM, HepG2, Hela, HL-60. All cell lines were purchased from ATCC (Manassas, Va., USA). Cells were cultured in RPMI-1640 or DMEM medium containing 10% (wt/wt) FBS and 1% (wt/wt) GlutaMax. Cells were distributed at 2,000-10,000 per well of a 384-well plate (Thermo Fisher Scientific, Waltham, USA) and incubated overnight. After 24 hours, test substance solutions (10 or 100 μmoll.Math.l.sup.−1) were added to the wells and the cells were incubated with the test substances at 37° C. and 5% (vol./vol.) CO.sub.2 for another 72 h. XTT dye (XTT cell proliferation kit II, Roche Diagnostics GmbH, Mannheim, Germany) was added to the wells according to the manufacturer's protocol. After one hour of incubation with the dye, the absorbance at 495 nm was measured and the signal was compared with the control (100% viability=cells without test substance).
[0255] Results of Cytotoxicity Testing on Human Tumour Cell Lines of Lymphoblastoid Leukaemia, Cervical Cancer, Liver Cancer and Myeloid Leukaemia
TABLE-US-00005 Cell viability [% vs. control] CEM HL60 HeLa S3 HepG2 Comp, 10 100 10 100 10 100 10 100 ID μM μM μM μM μM μM μM μM 3a 105 94 94 106 119 96 103 107 3b 106 88 88 100 106 78 97 92 3d 105 85 110 107 86 81 88 89 3e 108 85 101 106 104 86 92 90 3f 92 84 110 108 103 94 95 82 3g 106 73 100 103 98 89 93 63 3h 94 115 110 95 89 103 88 108 3i 93 117 111 100 78 105 87 110 3j 94 119 109 123 93 109 76 124 3k 110 123 112 103 104 94 109 105 3l 104 121 104 111 95 100 97 109 3m 97 120 102 124 108 104 91 105 5a 104 100 105 76 92 102 91 104 5b 90 109 111 86 93 101 83 106 5c 113 108 86 89 119 99 96 108 5d 89 107 112 95 95 96 82 89 5e 96 104 112 83 99 106 75 110 5f 98 72 114 98 96 100 78 121 5g 114 101 88 103 109 99 102 108 5h 114 103 109 106 116 93 112 105 5i 107 107 104 101 94 98 89 101 M = mol .Math. l.sup.−1
INDUSTRIAL APPLICABILITY
[0256] The substances disclosed in this application are useful as medicaments for the targeted treatment or diagnostic agents for the targeted diagnosis of tumour growth.