反応式
C[O:2][C:3]([C:5]1[NH:6][C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[C:9]([C:14]([F:17])([F:16])[F:15])[CH:8]=2)=[O:4].Br[CH2:19][C:20]1[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH:23]=[CH:22][CH:21]=1>>[C:20]1([CH2:19][N:6]2[C:7]3[C:12](=[CH:11][CH:10]=[C:9]([C:14]([F:17])([F:16])[F:15])[CH:8]=3)[CH:13]=[C:5]2[C:3]([OH:2])=[O:4])[C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH:23]=[CH:22][CH:21]=1参加物
3
実験手順
Using general procedure B, 6-trifluoromethyl-1H-indole-2-carboxylic acid methyl ester was coupled with 1-bromomethyl-naphthalene and the product obtained was hydrolyzed to give the title compound as white solid. MS: 368.0 ([M−H]−).
後処理
- customthe product obtained
出典と根拠
- ORDレコード
- ord-04b7fa227e3640c692e33a9783513999
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07696240B2
関連ノート
読み込み中…