1H-Pyrazole, 4-bromo-1-methyl- → HCID 66765337、化合物
反応式
[CH2:1]([O:3][C:4](=[O:26])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([S:14][C:15]2[C:23]3[C:18](=[CH:19][C:20]([Cl:24])=[CH:21][CH:22]=3)[NH:17][C:16]=2[CH3:25])[CH:7]=1)[CH3:2].Br[C:28]1[CH:29]=[N:30][N:31]([CH3:33])[CH:32]=1>>[CH2:1]([O:3][C:4](=[O:26])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([S:14][C:15]2[C:23]3[C:18](=[CH:19][C:20]([Cl:24])=[CH:21][CH:22]=3)[N:17]([C:28]3[CH:29]=[N:30][N:31]([CH3:33])[CH:32]=3)[C:16]=2[CH3:25])[CH:7]=1)[CH3:2]参加物
3
実験手順
Prepared according to the procedure described in Example 42, Step 4, using the following starting materials: [3-(6-chloro-2-methyl-1H-indol-3-ylsulfanyl)-4-methoxy-phenyl]-acetic acid ethyl ester and 4-bromo-1-methylpyrazole.
後処理
- customPrepared
出典と根拠
- ORDレコード
- ord-cb214c643c68415a8acdc404158cab48
- 出典データセット
- uspto-grants-2015_04