(1,1'-Bicyclohexyl)-4-one → 3-{[(1-Bicyclohexyl-4-yl-azetidin-3-ylcarbamoyl)-methyl]-amino}-5-trifluoromethyl-indazole-1-carboxylic acid isopropylamide
反応式
[CH:1]([NH:4][C:5]([N:7]1[C:15]2[C:10](=[CH:11][C:12]([C:16]([F:19])([F:18])[F:17])=[CH:13][CH:14]=2)[C:9]([NH:20][CH2:21][C:22](=[O:28])[NH:23][CH:24]2[CH2:27][NH:26][CH2:25]2)=[N:8]1)=[O:6])([CH3:3])[CH3:2].[CH:29]1([CH:36]2[CH2:41][CH2:40][CH2:39][CH2:38][CH2:37]2)[CH2:34][CH2:33][C:32](=O)[CH2:31][CH2:30]1>>[CH:1]([NH:4][C:5]([N:7]1[C:15]2[C:10](=[CH:11][C:12]([C:16]([F:18])([F:19])[F:17])=[CH:13][CH:14]=2)[C:9]([NH:20][CH2:21][C:22](=[O:28])[NH:23][CH:24]2[CH2:25][N:26]([CH:39]3[CH2:40][CH2:41][CH:36]([CH:29]4[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]4)[CH2:37][CH2:38]3)[CH2:27]2)=[N:8]1)=[O:6])([CH3:3])[CH3:2]参加物
3
実験手順
The title compound was prepared as a white solid from reaction of 3-[(azetidin-3-ylcarbamoylmethyl)-amino]-5-trifluoromethyl-indazole-1-carboxylic acid isopropylamide (as prepared in Example 90, Step A) and bicyclohexyl-4-one using the procedure described in Step E of Example 1.
出典と根拠
- ORDレコード
- ord-7894da8f7f864c50949cb2d17473e844
- 出典データセット
- uspto-grants-2013_05
- 特許番号
- US08436023B2
反応ノート
読み込み中…