tert-butyl N-(4-bromo-1-methyl-1H-pyrazol-5-yl)carbamate → 1-[4'-(5-tert-Butoxycarbonylamino-1-methyl-1H-pyrazol-4-yl)-biphenyl-4-yl]-cyclopropanecarboxylic acid ethyl ester
反応式
[C:1]([O:5][C:6](=[O:15])[NH:7][C:8]1[N:9]([CH3:14])[N:10]=[CH:11][C:12]=1Br)([CH3:4])([CH3:3])[CH3:2].[CH2:16]([O:18][C:19]([C:21]1([C:24]2[CH:29]=[CH:28][C:27]([C:30]3[CH:35]=[CH:34][C:33](B4OC(C)(C)C(C)(C)O4)=[CH:32][CH:31]=3)=[CH:26][CH:25]=2)[CH2:23][CH2:22]1)=[O:20])[CH3:17]>>[CH2:16]([O:18][C:19]([C:21]1([C:24]2[CH:25]=[CH:26][C:27]([C:30]3[CH:31]=[CH:32][C:33]([C:12]4[CH:11]=[N:10][N:9]([CH3:14])[C:8]=4[NH:7][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:15])=[CH:34][CH:35]=3)=[CH:28][CH:29]=2)[CH2:23][CH2:22]1)=[O:20])[CH3:17]参加物
3
反応物 2
生成物 1
実験手順
Prepared according to the procedure described in Example 5, Step 2, using the following starting materials: (4-bromo-2-methyl-2H-pyrazol-3-yl)-carbamic acid tert-butyl ester and 1-[4′-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-biphenyl-4-yl]-cyclopropanecarboxylic acid ethyl ester.
後処理
- customPrepared
出典と根拠
- ORDレコード
- ord-8590319ffd0b4ad88d82a16aaf40eb91
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09272990B2
反応ノート
読み込み中…