Malic Acid → HCID 12895722、化合物
反応式
C(O)C.[NH2:4][C:5]1[CH:25]=[CH:24][C:8]([C:9]([N:11]([CH:13]2[CH2:17][CH2:16][N:15]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[CH2:14]2)[CH3:12])=[O:10])=[CH:7][CH:6]=1.[C:26]([OH:34])(=[O:33])[CH:27]([CH2:29][C:30]([OH:32])=[O:31])[OH:28]>O>[C:26]([OH:34])(=[O:33])[CH:27]([CH2:29][C:30]([OH:32])=[O:31])[OH:28].[NH2:4][C:5]1[CH:6]=[CH:7][C:8]([C:9]([N:11]([CH:13]2[CH2:17][CH2:16][N:15]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[CH2:14]2)[CH3:12])=[O:10])=[CH:24][CH:25]=1参加物
5
実験手順
An ethanol solution containing 20.0 g. (0.067 mole) of 4-amino-N-(1-cyclohexyl-3-pyrrolidinyl)-N-methylbenzamide was treated with 4.94 g. (0.037 mole) of (-)-malic acid and the solution was refrigerated overnight. The crystalline material which separated (m.p. 147°-157° C.) was recrystallized twice from ethanol to give 5.0 g. crystals which melted at 162°-163° C. Rotation [α]D30 : -22.65 (water).