反応式
[C:1](Cl)(=[O:3])[CH3:2].[NH2:5][C:6]1[CH:7]=[C:8]([C:19]([O:21][CH3:22])=[O:20])[C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[Br:18])=[CH:10][CH:11]=1.C(N(CC)CC)C>C(OCC)C.C(OCC)(=O)C>[C:1]([NH:5][C:6]1[CH:7]=[C:8]([C:19]([O:21][CH3:22])=[O:20])[C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[Br:18])=[CH:10][CH:11]=1)(=[O:3])[CH3:2]参加物
6
実験手順
Acetyl chloride (70 mg, 63 μl, 0.89 mmol) was added to a solution of methyl 4-amino-2′-bromo-2-biphenylcarboxylate (227 mg, 0.74 mmol) and triethylamine (90 mg, 123 ul, 0.89 mmol) in diethyl ether (3 ml) and stirred at room temperature for 1 hour. The mixture was diluted with ethyl acetate(10 ml) and washed with 2M HCl, 5% NaHCO3, water and brine the organic phase was dried and evaporated to leave the title compound as a yellow oil (226 mg, 88%).
後処理
- washwashed with 2M HCl, 5% NaHCO3, water and brine the organic phase
- customwas dried
- customevaporated
出典と根拠
- ORDレコード
- ord-028f0a6b94334a54b8bbeb8546e3a98f
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07446222B2
関連ノート
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