반응식
[Cl-].[C:2]([NH:5][C:6]1[S:7][CH:8]=[C:9]([CH2:11][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[N:10]=1)(=[O:4])[CH3:3].CC(C)([O-])C.[K+].[CH:37]([C:39]1[S:43][C:42]([C:44]([OH:46])=[O:45])=[CH:41][CH:40]=1)=O.O>CN(C)C=O>[C:2]([NH:5][C:6]1[S:7][CH:8]=[C:9]([CH:11]=[CH:37][C:39]2[S:43][C:42]([C:44]([OH:46])=[O:45])=[CH:41][CH:40]=2)[N:10]=1)(=[O:4])[CH3:3]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of {[2-(acetylamino)-1,3-thiazol-4-yl]methyl}(triphenyl)phosphonium chloride (3.771 g, 8.325 mmol) in anhydrous N,N-dimethylformamide (35 ml) was added potassium tert-butoxide (2.515 g, 22.41 mmol) at 0° C., and the mixture was stirred for 15 min. 5-Formylthiophene-2-carboxylic acid (1.000 g, 6.404 mmol) was added by small portions, and the mixture was stirred at 0° C. for 30 min. The mixture was warmed to room temperature, stirred for 2 hr, and poured into iced water (300 ml). After stirring for 30 min, the mixture was washed twice with ethyl acetate. The aqueous layer was cooled to 0° C., and adjusted to pH 3 by dropwise addition of 6M hydrochloric acid. After stirring at 0-5° C. for 2 hr, the precipitated crystals were collected by filtration, washed 3 times with water, and twice with diisopropyl ether and dried under reduced pressure to give 5-{2-[2-(acetylamino)-1,3-thiazol-4-yl]vinyl}thiophene-2-carboxylic acid (1.104 g, 3.751 mmol, yield 58.6%) as a yellow ocher solid.
후처리
- stirringthe mixture was stirred at 0° C. for 30 min
- stirringstirred for 2 hr
- stirringAfter stirring for 30 min
- washthe mixture was washed twice with ethyl acetate
- temperatureThe aqueous layer was cooled to 0° C.
- additionadjusted to pH 3 by dropwise addition of 6M hydrochloric acid
- stirringAfter stirring at 0-5° C. for 2 hr
- filtrationthe precipitated crystals were collected by filtration
- washwashed 3 times with water
- dry with materialtwice with diisopropyl ether and dried under reduced pressure
출처 및 근거
- ORD 기록
- ord-e8dd722b52a647b88e8e9a2d0ea64d7b
- 출처 데이터셋
- uspto-grants-2013_08
- 특허 번호
- US08507690B2
연결된 노트
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