反応式
[CH2:1]([N:4]([CH:35]1[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]1)[C:5](=[O:34])[C:6]1[CH:11]=[C:10]([N:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][CH:20]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH2:14][CH2:13]2)[CH:9]=[CH:8][C:7]=1F)[CH:2]=[CH2:3].F[C:42]1[CH:50]=CC([N+]([O-])=O)=C[C:43]=1C(O)=O.C(NC1CCCCC1)C=C>>[CH2:1]([N:4]([CH:35]1[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]1)[C:5](=[O:34])[C:6]1[CH:11]=[C:10]([N:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][CH:20]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH2:14][CH2:13]2)[CH:9]=[CH:8][C:7]=1[CH:42]([CH3:50])[CH3:43])[CH:2]=[CH2:3]参加物
4
実験手順
Steps (a) and (b) of Example 59 were repeated, except that the compound prepared just above in step (a) was used instead of 2-fluoro-5-nitrobenzoic acid. Step (d) of Example 1 was then repeated, except that N-allylcyclohexylamine was used instead of N-methylbenzylamine. Thus, the title compound was prepared.
後処理
- customprepared just above in step (a)
出典と根拠
- ORDレコード
- ord-c81ce5498cca4b658ec1b00d9bacf2ba
- 出典データセット
- uspto-grants-2006_04
- 特許番号
- US07030120B2
関連ノート
読み込み中…