[NH2:1][C:2]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][CH:7]2[C:14]1[N:15]=[CH:16][N:17]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH:18]=1.N1C=CC=C[CH:27]=1.[CH3:32][S:33](Cl)(=[O:35])=[O:34]>ClCCl>[C:19]([O:21][CH2:22][CH3:25])(=[O:20])[CH3:27].[NH3:1].[CH3:13][O:12][C:9]1[CH:10]=[CH:11][C:2]([NH:1][S:33]([CH3:32])(=[O:35])=[O:34])=[C:3]2[C:8]=1[CH:7]([C:14]1[N:15]=[CH:16][N:17]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH:18]=1)[CH2:6][CH2:5][CH2:4]2A solution of Example 26D (0.50 g, 1.5 mmol) in dichloromethane (5 mL) was treated with pyridine (0.34 mL, 4.4 mmol), treated with methanesulfonyl chloride (0.17 mL, 2.2 mmol) and stirred for 1.5 hours. Purification of the mixture on silica gel eluting with ammonia-saturated dichloromethane and then with 10% ethyl acetate/ammonia-saturated dichloromethane provided the desired product which was dried under vacuum.
読み込み中…