Potassium Hydroxide → HCID 20292191、化合物
反応式
[C:1]([N:9]([CH2:16][CH2:17][CH2:18][CH3:19])[CH2:10][CH2:11][CH2:12][C:13]([OH:15])=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:20]([NH:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][C:39]([O:41]CC)=[O:40])([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[OH-].[K+]>C(O)C>[C:1]([N:9]([CH2:16][CH2:17][CH2:18][CH3:19])[CH2:10][CH2:11][CH2:12][C:13]([N:33]([CH:20]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][C:39]([OH:41])=[O:40])=[O:15])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
5
実験手順
Analogously to Example 1, by using equivalent quantities, reacting N-benzoyl-4-(n-butylamino)butyric acid and ethyl 6-benzhydrylaminocaproate and suitable processing, dissolving the evaporation residue in ethanol, adding an ethanolic solution of potassium hydroxide, stirring for 12 hours at room temperature and further processing yields N-[N-benzoyl-4-(n-butylamino)butyryl]-6-benzhydrylaminocaproic acid.