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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 749340생성일: 2026년 10월 23일

Acetic Acid → 5-(4-Fluoro-phenyl)-3-isopropylamino-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/ko/reaction/749340

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-MethoxypropeneHCID 8300—
반응물Sodium BicarbonateHCID 516892—
반응물Methyl 3-amino-5-(4-fluorophenyl)thiophene-2-carboxylateHCID 619692—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물5-(4-Fluoro-phenyl)-3-isopropylamino-thiophene-2-carboxylic acid methyl esterHCID 5975230191%

반응 단계

To a stirred solution of 3-Amino-5-(4-fluoro-phenyl)-thiophene-2-carboxylic acid methyl ester (500 mg, 2.0 mmol) in 1,2-dichloroethane (10 mL) was added sequentially 2-methoxypropene (0.76 mL, 8.0 mmol), AcOH (0.12 mL, 4.0 mmol) and NaBH(OAc)3 (0.848 mg, 8.0 mmol) and stirred for 16 h. It was then diluted with EtOAc and H2O. The aqueous solution was adjusted to pH=7 by adding NaHCO3. The aqueous phase was extracted with EtOAc, the combined extract was washed with brine and dried on MgSO4 and filtered. Purification on bond elute with hexane to 5% EtOAc-hexane furnished 5-(4-Fluoro-phenyl)-3-isopropylamino-thiophene-2-carboxylic acid methyl ester (0.530 mg, 91% yield). 1H NMR (CDCl3, 400 MHz): δ 7.62 (d, 2H), 7.09 (m, 2H), 6.81 (s, 1H), 3.84 (s, 3H), 3.71 (m, 1H), 1.35 (d, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402608B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-325ad75748e94949924704eea259da0a
출처 메모uspto-grants-2008_07