苯乙胺 → HCID 67239281，化合物
反应方程式
C1([CH2:7][CH:8]([NH:14][C:15](=[O:33])[C:16]2[CH:21]=[CH:20][CH:19]=[N:18][C:17]=2[N:22]2[CH:26]=[CH:25][C:24]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)=[N:23]2)[CH:9]([OH:13])[C:10]([OH:12])=O)C=CC=CC=1.[C:34]1([CH2:40][CH2:41][NH2:42])[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>>[OH:13][CH:9]([C:10](=[O:12])[NH:42][CH2:41][CH2:40][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)[CH:8]([NH:14][C:15](=[O:33])[C:16]1[CH:21]=[CH:20][CH:19]=[N:18][C:17]=1[N:22]1[CH:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[N:23]1)[CH2:7][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1参与物
3
实验过程
The reaction was carried out in analogy to reaction step 1.3 by reacting 4-phenyl-2-hydroxy-3-(2-(3-phenyl-1H-pyrazol-1-yl)nicotinamido)butanoic acid with 2-phenylethylamine; ESI-MS [M+H]+: 546.2
后处理
- customThe reaction was carried out in analogy to reaction step 1.3
来源与证据
- ORD记录
- ord-1c1d535204274f13afcc4bf394617797
- 来源数据集
- uspto-grants-2013_12