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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 449152생성일: 2026년 10월 24일

4-Methylmorpholine → [(R)-1-(3,5-Dichloro-4-fluoro-phenylcarbamoyl)-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/449152

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물3,5-Dichloro-4-fluoroanilineHCID 75948—
반응물BOC-D-alanineHCID 637606—
용매TetrahydrofuranHCID 8028—
생성물[(R)-1-(3,5-Dichloro-4-fluoro-phenylcarbamoyl)-ethyl]-carbamic acid tert-butyl esterHCID 67390502—

반응 조건

온도20 °C

반응 단계

To a cooled (−20° C.) solution of (R)-2-tert-butoxycarbonylamino-propionic acid (57.2 g, 302 mmol) in anhydrous THF (582 mL) was added N-methyl-morpholine (34.9 mL, 317 mmol) at a rate to keep the internal temperature at −15° C. Isobutyl chloroformate (42.0 mL, 317 mmol) was then added over a 20 min period and the resulting mixture was stirred for 30 min. A solution of 3,5-dichloro-4-fluoro-phenylamine (54.4 g, 302 mmol) in THF (160 mL) was then added over 40 min. The reaction mixture was warmed to 20° C. and stirred for 20 h. The reaction mixture was filtered and concentrated in vacuo. To the resulting oil was added MeOH (200 mL) and the solution was concentrated to provide the title compound as a tan colored solid, m/z 295.3 [M-t-Bu]+. This material was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481750B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-96938e9745c44d4e9167bfb93995cfb4
출처 메모uspto-grants-2013_07