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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1471780생성일: 2026년 10월 25일

Triethylamine → 4-[5-(4-Cyano-2-fluoro-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1471780

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Sodium BicarbonateHCID 516892—
반응물4-[5-(2-Fluoro-4-aminocarbonyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 71736417—
용매DichloromethaneHCID 6344—
생성물4-[5-(4-Cyano-2-fluoro-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 71736569—

반응 단계

Trifluoroacetic anhydride (26 μL) is added to a solution of 4-[5-(2-fluoro-4-aminocarbonyl-phenyl)-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester (40 mg) and triethylamine (51 μL) in dichloromethane (3 mL) at room temperature. The solution is stirred at room temperature for 2 h before another portion of trifluoroacetic anhydride (26 μL) and triethylamine (51 μL) is added. The solution is stirred for 0.5 h and then aqueous NaHCO3 solution is added. The resulting mixture is extracted with dichloromethane and the combined extracts are washed with brine, dried (Na2SO4), and concentrated. The residue is triturated with ether and then with methanol to give the title compound. LC (method 3): tR=1.52 min; Mass spectrum (ESI+): m/z=422 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012456B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-41efc0da41dc4e89ab31ef13c9683ab2
출처 메모uspto-grants-2015_04