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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339111생성일: 2026년 10월 23일

Hydrochloric Acid → tert-Butyl 2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1-benzofuran-6-carboxylate

https://huagongshe.com/ko/reaction/339111

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrateHCID 23149411—
반응물2,2,2-Trifluoro-1-(3-(trifluoromethyl)phenyl)ethanamineHCID 43825172—
반응물6-(tert-Butoxycarbonyl)-1-benzofuran-2-carboxylic acidHCID 58247976—
용매DimethylformamideHCID 6228—
생성물tert-Butyl 2-({2,2,2-trifluoro-1-[3-(trifluoromethyl)phenyl]ethyl}carbamoyl)-1-benzofuran-6-carboxylateHCID 58247936—

반응 조건

온도50 °C

반응 단계

A solution of 6-(tert-butoxycarbonyl)-1-benzofuran-2-carboxylic acid (350 mg, 1.33 mmol) and 2,2,2-trifluoro-1-[3-trifluoromethylphenyl]ethanamine (357 mg, 1.46 mmol) in N,N-dimethylformamide (5 ml) was admixed with 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (304 mg, 1.46 mmol) and stirred in a closed vessel at 50° C. overnight. The cooled reaction solution was admixed with hydrochloric acid (1 M) and extracted with ethyl acetate. The organic phase was washed with sat. sodium hydrogencarbonate solution and saturated sodium chloride solution, dried over sodium sulphate, filtered and concentrated to dryness under reduced pressure. This leaves 453 mg as a mixture of the tert-butyl ester and of the free acid, which was used for the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889878B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-1fe95d17e6f14f408ace0eabd2277447
출처 메모uspto-grants-2014_11