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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390127생성일: 2026년 10월 24일

4-Nitro-benzoic acid 5-(1-ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-1-[hept-6-enyl-(4-methoxy-benzyl)-carbamoyl]-pyrrolidin-3-yl ester → 14-(4-Methoxy-benzyl)-18-(4-nitro-benzoyloxy)-2,15-dioxo-3,14,16-triaza-tricyclo[14.3.0.0*4,6*]nonadec-7-ene-4-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/390127

반응식

참여 물질

역할이름HCID투입량
반응물4-Nitro-benzoic acid 5-(1-ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-1-[hept-6-enyl-(4-methoxy-benzyl)-carbamoyl]-pyrrolidin-3-yl esterHCID 66870506—
촉매(1,3-Bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene)(dichloro)((2-((propan-2-yl)oxy)phenyl)methylidene)rutheniumHCID 11763533—
용매1,2-DichloroethaneHCID 11—
생성물14-(4-Methoxy-benzyl)-18-(4-nitro-benzoyloxy)-2,15-dioxo-3,14,16-triaza-tricyclo[14.3.0.0*4,6*]nonadec-7-ene-4-carboxylic acid ethyl esterHCID 66870501—

반응 단계

The diene 21d (406 mg, 0.6 mmol) was dissolved in DCE (250 ml) and degassed. Hoveyda-Grubbs Catalyst 2nd generation (26 mg, 0.042 mmol) was added and the solution was heated to reflux. After 3 h the solution was evaporated and used direct in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383584B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-4efa5432b94e43bdad6d26b0c1c5878a
출처 메모uspto-grants-2013_02