Potassium Carbonate → HCID 59627213、化合物

反応式

CS(O[CH2:6][CH2:7][CH2:8][C@:9]1([C:25]2[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=2)[CH2:14][CH2:13][N:12]([C@H:15]([C:17]2[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][CH:18]=2)[CH3:16])[C:11](=[O:24])[NH:10]1)(=O)=O.[CH3:32][S:33]([NH2:36])(=[O:35])=[O:34].C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[Br:23][C:20]1[CH:21]=[CH:22][C:17]([C@@H:15]([N:12]2[CH2:13][CH2:14][C@:9]([CH2:8][CH2:7][CH2:6][NH:36][S:33]([CH3:32])(=[O:35])=[O:34])([C:25]3[CH:30]=[CH:29][C:28]([F:31])=[CH:27][CH:26]=3)[NH:10][C:11]2=[O:24])[CH3:16])=[CH:18][CH:19]=1

参加物

実験手順

To a solution of 3-((R)-1-((S)-1-(4-bromophenyl)ethyl)-4-(4-fluorophenyl)-2-oxohexa hydropyrimidin-4-yl)propyl methanesulfonate (58 mg, 0.11 mmol) and methanesulfonamide (105 mg, 1.10 mmol) in acetone (10 mL) was added K2CO3 (31 mg, 0.22 mmol), and the mixture was refluxed overnight. The reaction was quenched with water, and the mixture was extracted with EtOAc. After removal of the solvent, the mixture was extracted with EtOAc, and the organic solution was washed with brine, dried over Na2SO4, filtered and concentrated to give the crude product, which was purified by preparative TLC and preparative HPLC to give N-(3-((R)-1-((S)-1-(4-bromophenyl)ethyl)-4-(4-fluorophenyl)-2-oxohexahydropyrimidin-4-yl)propyl)methanesulfonamide (8 mg, 14%). 1H NMR (CDCl3): 1.18□m, 1H), 1.45 (d, 3H), 1.50 (m, 1H), 1.88-2.16 (m, 5H), 2.84 (m, 4H), 3.02 (m, 2H), 4.70 (s, 1H), 5.63 (m, 1H), 6.88-6.98 (m, 4H), 7.12 (m, 2H), 7.30 (m, 2H). LC-MS Method 1 tR=1.146 min, m/z=512.