O.[NH2:2][CH:3]1[CH2:8][CH2:7][N:6]([CH2:9][CH2:10][C:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[NH:13][CH:12]=2)[CH2:5][CH2:4]1.C(N(CC)CC)C.Cl[CH2:28][C:29]([NH:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)=[O:30].O>CN(C)C=O>[NH:31]([C:29]([CH2:28][NH:2][CH:3]1[CH2:8][CH2:7][N:6]([CH2:9][CH2:10][C:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[NH:13][CH:12]=2)[CH2:5][CH2:4]1)=[O:30])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=13-[2-(4-Amino-1-piperidyl) ethyl]indole hydrate (1.31g.) was dissolved in dimethylformamide (15 ml) containing triethylamine (2 ml) and chloroacetanilide (0.85g) added. The mixture was stirred for 24 hours, poured into water (100 ml) and extracted with chloroform (2 × 50 ml). The combined chloroform layers were washed with water, dried (MgSO4), filtered and evaporated to give the title compound as an amber oil (2.06 g). This was converted to the hydrochloride (1.29 g), m.p. 240.7°, on addition of EtOH-HC1 and Et2O.
読み込み中…