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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1433746생성일: 2026년 10월 23일

Pyridine → (1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/1433746

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Cyanuric fluorideHCID 12664—
반응물(2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acidHCID 7021178—
용매DichloromethaneHCID 6344—
생성물(1-Fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl esterHCID 87517560—

반응 단계

To a solution of (2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyric acid (838 mg, 3.0 mmol) in dichloromethane (10 mL) at −35° C. was added dry pyridine (255 μL, 3.15 mmol) and cyanuric fluoride (375 μL, 4.5 mmol) under an atmosphere of dry argon. The mixture was stirred for 1.5 hours while maintaining the temperature between −35 and −25° C. A small amount of ice was added to the reaction mixture and the mixture stirred vigorously for 15 minutes. The organic layer was decanted away from the aqueous solution and the aqueous layer extracted with dichloromethane (2×10 mL). The combined organic layers were washed with ice cold water (15 mL), dried over sodium sulfate, filtered and concentrated in vacuo to give (1-fluorocarbonyl-2-phenyl-propyl)-carbamic acid tert-butyl ester which was used in the subsequent step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612212B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-0dfd7448cbba4e059c35e0105354547d
출처 메모uspto-grants-2009_11