反応式
[NH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1)[NH2:2].C(=O)([O-])[O-].[Cs+].[Cs+].F[C:19]1[CH:26]=[CH:25][C:24]([I:27])=[CH:23][C:20]=1[CH:21]=O.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CN1CCCC1=O>[I:27][C:24]1[CH:23]=[C:20]2[C:19](=[CH:26][CH:25]=1)[N:1]([C:3]1[CH:4]=[CH:5][C:6]([C:7]([OH:9])=[O:8])=[CH:10][CH:11]=1)[N:2]=[CH:21]2参加物
実験手順
4-Hydrazinobenzoic acid (11.32 g, 60 mmol) and cesiumcarbonate (58.65 g, 180 mmol) are added to 2-fluoro-5-iodobenzaldehyde (15 g, 60 mmol) in 300 mL N-methylpyrrolidon. After 1 h stirring at r.t., the reaction is heated for 4 h at 150° C. The reaction mixture is allowed to cool off and poured on 1 L ice water. The reaction mixture is acidified with citric acid and vigorously stirred at r.t. for 30 min. The precipitate is filtered off and given in ethyl acetate. The slurry is vigorously stirred for 1 h and sucked off. The filter residue (few material) is discarded and the filtrate evaporated. This residue which is contaminated with N-methylpyrrolidine is treated with 300 mL of a mixture of ethyl acetate/hexane (1:3) and stirred overnight. The precipitated crystals are sucked off and dried. 17.11 g (78.32%) of 4-(5-iodoindazole-1-yl)-benzoic acid are obtained.
後処理
- temperaturethe reaction is heated for 4 h at 150° C
- temperatureto cool off
- stirringvigorously stirred at r.t. for 30 min
- filtrationThe precipitate is filtered off
- stirringThe slurry is vigorously stirred for 1 h
- customthe filtrate evaporated
- additionis treated with 300 mL of a mixture of ethyl acetate/hexane (1:3)
- stirringstirred overnight
- customdried
出典と根拠
- ORDレコード
- ord-3020b7422e30417da0ba59e237a7512a
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07728030B2
関連ノート
読み込み中…