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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2371327생성일: 2026년 10월 26일

Benzyl chloroformate → (7S,10S,13S)-13-Benzyloxycarbonylamino-10-isobutyl-9,12-dioxo-2-oxa-8,11-diaza-bicyclo-[13.2.2]nonadeca-1(18),15(19),16-triene-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/2371327

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl chloroformateHCID 10387—
반응물DiisopropylethylamineHCID 81531—
반응물Dichloromethane ethylacetateHCID 21226138—
반응물(7S,10S,13S)-13-Amino-10-isopropyl-9,12-dioxo-2-oxa-8,11-diaza-bicyclo[13.2.2]nonadeca-1-(18),15(19),16-triene-7-carboxylic acid methyl ester hydrogen chloride saltHCID 86650244—
용매DimethylformamideHCID 6228—
생성물(7S,10S,13S)-13-Benzyloxycarbonylamino-10-isobutyl-9,12-dioxo-2-oxa-8,11-diaza-bicyclo-[13.2.2]nonadeca-1(18),15(19),16-triene-7-carboxylic acid methyl esterHCID 44191155—

반응 단계

Amine 47 (65 mg) was dissolved in anhydrous DMF (30 mL). Benzyl chloroformate (0.29 mL) and DIPEA (0.75 mL) were added and the reaction mixture was stirred at rt for 18 h before being partitioned between chloroform and 1M hydrochloric acid. The aqueous phase was extracted three more times with chloroform and the combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. Purification was achieved using flash chromatography, eluting with a gradient of 15% EtOAc/DCM to 50% EtOAc/DCM to yield an off-white solid, 54 mg, 70%. Rf=0.33 (30% EtOAc/DCM).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08710178B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-028affbd831f4a298fda6f3bde9da8b2
출처 메모uspto-grants-2014_04