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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2371325생성일: 2026년 10월 26일

(E)-(7S,10S,13S)-13-tert-Butoxycarbonylamino-10-isopropyl-9,12-dioxo-2-oxa-8,11-diazabicyclo[13.2.2]nonadeca-1(18),4,15(19),16-tetraene-7-carboxylic acid methyl ester → (7S,10S,13S)-13-tert-Butoxycarbonylamino-10-isopropyl-9,12-dioxo-2-oxa-8,11-diazabicyclo[13.2.2]nonadeca-1(18),15(19),16-triene-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/2371325

반응식

참여 물질

역할이름HCID투입량
반응물(E)-(7S,10S,13S)-13-tert-Butoxycarbonylamino-10-isopropyl-9,12-dioxo-2-oxa-8,11-diazabicyclo[13.2.2]nonadeca-1(18),4,15(19),16-tetraene-7-carboxylic acid methyl esterHCID 66847119—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물(7S,10S,13S)-13-tert-Butoxycarbonylamino-10-isopropyl-9,12-dioxo-2-oxa-8,11-diazabicyclo[13.2.2]nonadeca-1(18),15(19),16-triene-7-carboxylic acid methyl esterHCID 66847442—

반응 단계

Olefin 45 (1.36 g, 2.70 mmol) was dissolved in 40 mL of EtOAc. 10% palladium on carbon catalyst was added (25%) and the reaction mixture was subjected to hydrogenation at rt and atmospheric pressure for 18 h before being filtered through celite and concentrated in vacuo to yield a brown solid, 1.36 g, 100%. m.p. 225-228° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08710178B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-7f723ac189334cb39cb4196288b74cdd
출처 메모uspto-grants-2014_04