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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 475018생성일: 2026년 10월 24일

4-(4-Fluorobenzyloxy)-1h-pyridin-2-one → tert-Butyl 2-(4-(4-fluorobenzyloxy)-2-oxopyridin-1(2H)-yl)-10-methyl-7,8,9,10-tetrahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepine-6(5H)-carboxylate

https://huagongshe.com/ko/reaction/475018

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-Fluorobenzyloxy)-1h-pyridin-2-oneHCID 22049900—
반응물tert-butyl 2-bromo-10-methyl-7,8,9,10-tetrahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepine-6(5H)-carboxylateHCID 86649551—
생성물tert-Butyl 2-(4-(4-fluorobenzyloxy)-2-oxopyridin-1(2H)-yl)-10-methyl-7,8,9,10-tetrahydropyrido[3',2':4,5]pyrrolo[3,2-c]azepine-6(5H)-carboxylateHCID 7080521196.4%

반응 단계

tert-Butyl 2-bromo-10-methyl-7,8,9,10-tetrahydropyrido[3′,2′:4,5]pyrrolo[3,2-c]azepine-6(5H)-carboxylate (147 mg, 0.386 mmol) and 4-(4-fluorobenzyloxy)pyridin-2(1H)-one (93 mg, 0.43 mmol) were reacted following the procedure for Example 2 (step d) to provide the title compound (193 mg, 96%) as a yellow oil: ESI MS m/z 519 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637501B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-26a3337f07a64d908a49cfc6d6815a66
출처 메모uspto-grants-2014_01