[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[OH:11][C@@H:12]1[CH2:16][CH2:15][CH2:14][C@@H:13]1[NH:17][C:18](=[O:30])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[N:25]1[N:29]=[CH:28][CH:27]=[N:26]1.Cl[C:32]1[CH:37]=[N:36][C:35]([C:38]([F:41])([F:40])[F:39])=[CH:34][N:33]=1>C1COCC1>[N:29]1[N:25]([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[C:18]([NH:17][C@H:13]2[CH2:14][CH2:15][CH2:16][C@H:12]2[O:11][C:32]2[CH:37]=[N:36][C:35]([C:38]([F:41])([F:40])[F:39])=[CH:34][N:33]=2)=[O:30])[N:26]=[CH:27][CH:28]=1LiHMDS in THF (1.0 M, 0.477 ml, 0.477 mmol) was added to a solution of N-[(1S,2R)-2-hydroxycyclopentyl]-2-(2H-1,2,3-triazol-2-yl)benzamide (Intermediate 10; 0.100 g, 0.37 mmol) in THF (3 ml) at 0° C. under nitrogen. The reaction was stirred at this temperature for 1 hour and then 2-chloro-5-(trifluoromethyl)pyrazine (CAS number 799557-87-2; 0.059 ml, 0.48 mmol) was added. The mixture was allowed to warm to room temperature and stirred for 5 hours. The reaction was then quenched with water (2 ml) and extracted with ethyl acetate (30 ml). The organics were washed with brine (10 ml), dried over magnesium sulfate and concentrated in vacuo. The crude product was purified by column chromatography (silica, 0-50% ethyl acetate/petrol) to afford the title compound.
불러오는 중…