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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 475017생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/475017

반응식

참여 물질

역할이름HCID투입량
반응물4-(4-Fluorobenzyloxy)-1h-pyridin-2-oneHCID 22049900—
반응물tert-butyl 2-bromo-10-methyl-5,8,9,10-tetrahydropyrido[3',2':4,5]pyrrolo[2,3-d]azepine-7(6H)-carboxylateHCID 58093388—
생성물tert-Butyl 2-(4-(4-fluorobenzyloxy)-2-oxopyridin-1(2H)-yl)-10-methyl-5,8,9,10-tetrahydropyrido[3',2':4,5]pyrrolo[2,3-d]azepine-7(6H)-carboxylateHCID 5809332362%

반응 단계

tert-Butyl 2-bromo-10-methyl-5,8,9,10-tetrahydropyrido[3′,2′:4,5]pyrrolo[2,3-d]azepine-7(6H)-carboxylate (120 mg, 0.316 mmol) and 4-(4-fluorobenzyloxy)pyridin-2(1H)-one (76 mg, 0.35 mmol) were reacted following the procedure for Example 2 (step d) to provide the title compound (100 mg, 62%) as a white solid: 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-967e53c24cdd4f3daf2cbaf10b05e8a4
출처 메모uspto-grants-2014_01