1,3-dimethyl-1H-pyrazole-4-carbaldehyde → methyl 10-bromo-3-((1,3-dimethyl-1H-pyrazol-4-yl)(hydroxy)methyl)-9-fluoro-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxylate
反応式
[Br:1][C:2]1[C:3]([F:20])=[CH:4][C:5]2[O:11][CH2:10][CH2:9][N:8]3[CH:12]=[C:13]([C:15]([O:17][CH3:18])=[O:16])[N:14]=[C:7]3[C:6]=2[CH:19]=1.[CH3:21][N:22]1[CH:26]=[C:25]([CH:27]=[O:28])[C:24]([CH3:29])=[N:23]1>>[Br:1][C:2]1[C:3]([F:20])=[CH:4][C:5]2[O:11][CH2:10][CH2:9][N:8]3[C:12]([CH:27]([C:25]4[C:24]([CH3:29])=[N:23][N:22]([CH3:21])[CH:26]=4)[OH:28])=[C:13]([C:15]([O:17][CH3:18])=[O:16])[N:14]=[C:7]3[C:6]=2[CH:19]=1参加物
3
反応物 2
生成物 1
実験手順
Methyl 10-bromo-3-((1,3-dimethyl-1H-pyrazol-4-yl)(hydroxy)methyl)-9-fluoro-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxylate was prepared similarly according to the procedure in Example 9. methyl 10-bromo-9-fluoro-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxylate was reacted with 1,3-dimethyl-1 h-pyrazole-4-carbaldehyde to afford the crude title compound which was carried forward without further purification.
後処理
- customMethyl 10-bromo-3-((1,3-dimethyl-1H-pyrazol-4-yl)(hydroxy)methyl)-9-fluoro-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine-2-carboxylate was prepared similarly
出典と根拠
- ORDレコード
- ord-e774ca58689d4ffb83a668480f7ba0d1
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09034866B2
反応ノート
読み込み中…