4-Ethoxycarbonylphenylboronic acid → 1-((4'-(Ethoxycarbonyl)-[1,1'-biphenyl]-2-yl)methyl)-2,3-dimethyl-1H-indole-5-carboxylic acid
反応式
Br[C:2]1[CH:22]=[CH:21][CH:20]=[CH:19][C:3]=1[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][C:10]([C:14]([OH:16])=[O:15])=[CH:11][CH:12]=2)[C:7]([CH3:17])=[C:6]1[CH3:18].[CH2:23]([O:25][C:26]([C:28]1[CH:33]=[CH:32][C:31](B(O)O)=[CH:30][CH:29]=1)=[O:27])[CH3:24]>>[CH2:23]([O:25][C:26]([C:28]1[CH:33]=[CH:32][C:31]([C:2]2[CH:22]=[CH:21][CH:20]=[CH:19][C:3]=2[CH2:4][N:5]2[C:13]3[C:8](=[CH:9][C:10]([C:14]([OH:16])=[O:15])=[CH:11][CH:12]=3)[C:7]([CH3:17])=[C:6]2[CH3:18])=[CH:30][CH:29]=1)=[O:27])[CH3:24]参加物
3
実験手順
The title compound was prepared following the same protocol as described in Step 5, Example 38, using 1-(2-bromobenzyl)-2,3-dimethyl-1H-indole-5-carboxylic acid instead of the (S)-1-(4-bromobenzyl)-N-(1-(4-nitrophenyl)ethyl)-1H-indole-5-carboxamide and the (4-(ethoxycarbonyl)phenyl)boronic acid instead of the phenylboronic acid. ESI-MS (m/z): 428 [M+H]+.
出典と根拠
- ORDレコード
- ord-d2c3f8d3c526471f87514446ecb851f7
- 出典データセット
- uspto-grants-2015_02