Ethanolamine → 4-(2-Hydroxy-ethylamino)-N-{[1-(4-phenyl-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide
反応式
F[C:2]1[CH:30]=[CH:29][C:5]([C:6]([NH:8][CH2:9][C:10](=[O:28])[NH:11][CH:12]2[CH2:15][N:14]([CH:16]3[CH2:21][CH2:20][CH:19]([C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=4)[CH2:18][CH2:17]3)[CH2:13]2)=[O:7])=[CH:4][C:3]=1[C:31]([F:34])([F:33])[F:32].[NH2:35][CH2:36][CH2:37][OH:38]>>[OH:38][CH2:37][CH2:36][NH:35][C:2]1[CH:30]=[CH:29][C:5]([C:6]([NH:8][CH2:9][C:10](=[O:28])[NH:11][CH:12]2[CH2:13][N:14]([CH:16]3[CH2:21][CH2:20][CH:19]([C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=4)[CH2:18][CH2:17]3)[CH2:15]2)=[O:7])=[CH:4][C:3]=1[C:31]([F:34])([F:33])[F:32]参加物
3
実験手順
The title compound was prepared as a white solid from the coupling of 4-fluoro-N-{[1-(4-phenyl-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide (as prepared in Example 71) and 2-amino-ethanol (Aldrich) using the procedure described in Example 65.
出典と根拠
- ORDレコード
- ord-cdad80112d8d432b949e2a01f6ae12a9
- 出典データセット
- uspto-grants-2013_08