Water → 3-(3-Cyano-4-methoxy-5-trifluoromethylbenzoyl)-5-trifluoromethyl-2,3-dihydro-1,3-benzothiazole
反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[CH:5][C:6]2[S:10][CH2:9][NH:8][C:7]=2[CH:11]=1.C(N(CC)CC)C.[C:21]([C:23]1[CH:24]=[C:25]([CH:29]=[C:30]([C:34]([F:37])([F:36])[F:35])[C:31]=1[O:32][CH3:33])[C:26](Cl)=[O:27])#[N:22].O>ClCCl>[C:21]([C:23]1[CH:24]=[C:25]([CH:29]=[C:30]([C:34]([F:35])([F:37])[F:36])[C:31]=1[O:32][CH3:33])[C:26]([N:8]1[C:7]2[CH:11]=[C:3]([C:2]([F:1])([F:12])[F:13])[CH:4]=[CH:5][C:6]=2[S:10][CH2:9]1)=[O:27])#[N:22]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
5-trifluoromethyl-2,3-dihydro-1,3-benzothiazole was dissolved in dichloromethane (5 mL), and triethylamine (0.56 mL) and 3-cyano-4-methoxy-5-trifluoromethylbenzoyl chloride (839 mg) were added to the solution, and then the mixture was stirred at room temperature for 1.5 hours. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1) to obtain the title compound (479 mg) as a pale yellow amorphous product.
後処理
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine
- dry with materialdried over anhydrous sodium sulfate
- distillationThe solvent was distilled off under reduced pressure
- customthe obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1)
出典と根拠
- ORDレコード
- ord-ab18ed94e23845379868f33a23005a84
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367843B2
反応ノート
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