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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1175429생성일: 2026년 10월 25일

4-chloro-2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R)-1-methyl-2-(triphenylmethoxy)ethoxy]-pyrimidine → 5-cyano-N-{2-[(2,3-difluorobenzyl)thio]-6-[(1R)-1-methyl-2-(triphenylmethyloxy)ethoxy]pyrimidin-4-yl}furan-2-sulfonamide

https://huagongshe.com/reaction/1175429

반응식

참여 물질

역할이름HCID투입량
반응물4-chloro-2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R)-1-methyl-2-(triphenylmethoxy)ethoxy]-pyrimidineHCID 53628345—
반응물5-Cyanofuran-2-sulfonamideHCID 53628369—
생성물5-cyano-N-{2-[(2,3-difluorobenzyl)thio]-6-[(1R)-1-methyl-2-(triphenylmethyloxy)ethoxy]pyrimidin-4-yl}furan-2-sulfonamideHCID 53628368—

반응 단계

The subtitle compound was prepared from 5-cyanofuran-2-sulfonamide (the product of step i) (0.29 g) and 4-chloro-2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R)-1-methyl-2-(triphenylmethoxy)ethoxy]-pyrimidine (the product of Example 13, step ii) (0.15 g) according to the procedure outlined in Example 1, step iv). Purification was by column chromatography on silica gel using EtOAc/isohexane (1:4 to 2:3 gradient) to give the subtitle compound as a pale yellow solid. Yield: 0.25 g

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07838675B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-9ff48a16dc5a42bcad0e2a3a807d3ace
출처 메모uspto-grants-2010_11