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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250632생성일: 2026년 10월 25일

1H-Pyrrolo(2,3-b)pyridine → N-[3-(5-chloro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluoro-phenyl]-3,5-difluorobenzenesulfonamide

https://huagongshe.com/reaction/250632

반응식

참여 물질

역할이름HCID투입량
반응물1H-Pyrrolo(2,3-b)pyridineHCID 9222—
반응물Sulfuryl chlorideHCID 24648—
반응물3,5-Difluorobenzenesulfonyl chlorideHCID 2774058—
반응물5-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 24229213—
반응물(3-Amino-2,6-difluorophenyl)(1H-pyrrolo[2,3-b]pyridin-3-yl)methanoneHCID 58086044—
생성물N-[3-(5-chloro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4-difluoro-phenyl]-3,5-difluorobenzenesulfonamideHCID 58086516—

반응 단계

Additional compounds were prepared following the protocol of Scheme 67 Step 6, optionally substituting (3-Amino-2,6-difluoro-phenyl)-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone P-1801 with (3-Amino-2,6-difluoro-phenyl)-(1H-pyrrolo[2,3-b]pyridin-3-yl)-methanone P-2021 (prepared per Scheme 67 Steps 1-5, substituting 5-chloro-1H-pyrrolo[2,3-b]pyridine 80 with 1H-pyrrolo[2,3-b]pyridine 94 in Step 3) and/or 3,5-difluorobenzenesulfonyl chloride 610 with an appropriate sulfonyl chloride. The following compounds were prepared by this procedure:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863288B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-4dbd065376c34c6fb7d4dd96c791eec5
출처 메모uspto-grants-2011_01