Cyclopropylamine → HCID 67113069、化合物
反応式
[NH2:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:19]=[CH:18][C:14]([C:15]([OH:17])=O)=[CH:13][CH:12]=1)[CH:6]=[CH:5]2.[CH:20]1([NH2:23])[CH2:22][CH2:21]1.[OH:24][CH2:25][CH2:26][N:27]([C:29]1[CH:37]=[CH:36][C:32]([C:33](O)=[O:34])=[CH:31][CH:30]=1)[CH3:28]>>[CH:20]1([NH:23][C:15](=[O:17])[C:14]2[CH:18]=[CH:19][C:11]([N:7]3[C:8]4[C:4](=[CH:3][C:2]([NH:1][C:33](=[O:34])[C:32]5[CH:31]=[CH:30][C:29]([N:27]([CH2:26][CH2:25][OH:24])[CH3:28])=[CH:37][CH:36]=5)=[CH:10][CH:9]=4)[CH:5]=[CH:6]3)=[CH:12][CH:13]=2)[CH2:22][CH2:21]1参加物
4
実験手順
Compound 952 was prepared according to the procedure described in Scheme IV from 4-(5-amino-1H-indol-1-yl)benzoic acid, cyclopropaneamine, and 4-(N-2-hydroxyethyl-N-methylamino)benzoic acid. [M+H]+ calcd for C28H28N4O3: 469.22; found 468.96.
出典と根拠
- ORDレコード
- ord-25d6cacd52c44179b9f5ddecc1d0645e
- 出典データセット
- uspto-grants-2015_09