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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1483228생성일: 2026년 10월 27일

4-(Trifluoromethyl)aniline → 6-Ethyl-2-({[4-(trifluoromethyl)phenyl]carbamoyl}amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamide

https://huagongshe.com/reaction/1483228

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)anilineHCID 9964—
반응물TriphosgeneHCID 94429—
반응물Sodium BicarbonateHCID 516892—
반응물2-Amino-6-ethyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamideHCID 614439—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물6-Ethyl-2-({[4-(trifluoromethyl)phenyl]carbamoyl}amino)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamideHCID 2523845631%

반응 단계

A vigorously stirred solution of 4-trifluoromethyl aniline (161 mg, 1.0 mmol) in DCM (3 mL) at room temperature was treated with aq. NaHCO3 (3 mL) and triphosgene (98 mg, 0.33 mmol) and the reaction mixture was vigorously stirred at room temperature for 45 min. 2-Amino-6-ethyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxamide (225 mg, 1.0 mmol) was next added followed by THF and the reaction mixture was stirred at room temperature for 8 h. The solvent was then removed under vacuo and the resultant crude product was diluted with methanol and the insoluble solid was filtered off. Upon evaporation of MeOH, the crude oil was taken up in DCM and washed with water (×2), and the aqueous layer was back extracted with DCM. All organics were combined, dried (Na2SO4) and concentrated using a rotary evaporator. The crude product was purified by flash chromatography, Isolera system (SiO2 gel as stationary phase, 12 g HP column, dry loading) using DCM-DCM/MeOH (0%-10% MeOH in DCM) to afford the title compound as a brown solid (128 mg, 31% yield). MS (M+H) 413.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09416141B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-8b471816f65e4b6996d5a00a3cf16823
출처 메모uspto-grants-2016_08