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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 500813생성일: 2026년 10월 24일

2,6-Dichloro-4-nitrophenol → (7-(2,6-Dichloro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanone

https://huagongshe.com/ko/reaction/500813

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dichloro-4-nitrophenolHCID 12066—
반응물(7-Chlorothieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanoneHCID 11173165—
반응물7-(2-fluoro-4-nitrophenoxy)-N,N-dimethylthieno[3,2-b]pyridine-2-carboxamideHCID 59424475—
생성물(7-(2,6-Dichloro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)(pyrrolidin-1-yl)methanoneHCID 5942469469%

반응 단계

Starting from the compound 139 and following the procedure described above for the synthesis of compound 6 (scheme 1, example 1) but replacing 2-fluoro-4-nitrophenol with 2,6-dichloro-4-nitrophenol, title compound 140 was obtained in 69% yield. LRMS (M+1) 438.0 (100%), 439.1 (20%), 440.1 (70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772247B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-5e26d3efa8bf46d7bbaf674d75fe4a30
출처 메모uspto-grants-2010_08