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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1260602생성일: 2026년 10월 26일

2-Chloro-p-toluenesulfochloride → [1-(3-chloro-4-methyl-benzenesulfonyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/1260602

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-p-toluenesulfochlorideHCID 259744—
반응물2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
반응물methyl 2-(2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetateHCID 67218699—
용매DimethylformamideHCID 6228—
생성물[1-(3-chloro-4-methyl-benzenesulfonyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl esterHCID 67219360—

반응 단계

To a solution of (2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-acetic acid methyl ester (0.06 g, 0.294 mmol) in DMF (0.5 mL) is added a solution of BEMP (0.136 mL, 0.47 mmol) in DMF (0.5 mL). After 1 hour, a solution of 3-chloro-4-methyl-benzenesulfonyl chloride (0.105 g, 0.47 mmol) in DMF (0.5 mL) is added. The reaction mixture is stirred at room temperature overnight, then concentrated under reduced pressure to a minimum volume. The residue is loaded on a pre-packed Isolute™ silica column and eluted using a gradient eluent from 100% iso-hexane to 30% ethyl acetate in iso-hexane to afford [1-(3-chloro-4-methyl-benzenesulfonyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester; MH+=393.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08470848B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-01a3ce171b234499b3abf4fa4e55c24f
출처 메모uspto-grants-2013_06