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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1260641생성일: 2026년 10월 25일

Sodium Iodide → [1-(2-Chloro-4-ethanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl ester

https://huagongshe.com/reaction/1260641

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium hydrideHCID 24758—
반응물methyl 2-(2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetateHCID 67218699—
반응물1-Bromomethyl-2-chloro-4-ethanesulfonyl-benzeneHCID 67219826—
용매DimethylformamideHCID 6228—
생성물[1-(2-Chloro-4-ethanesulfonyl-benzyl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl]-acetic acid methyl esterHCID 67219537—

반응 단계

To an ice cooled (0° C.) stirred solution of (2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-acetic acid methyl ester ((2.68 g, 13.1 mmol) in dry DMF (95 ml) is added sodium hydride (577 mg of a 60% dispersion in mineral oil, 14.41 mmol). After stirring at room temperature for 1.5 hours, the reaction mixture is re-cooled to 0° C. and treated with 1-bromomethyl-2-chloro-4-ethanesulfonyl-benzene (6.6 g, 22.2 mmol) and sodium iodide (3.3 g, 22.2 mmol). The resulting mixture is stirred and allowed to warm to room temperature overnight. The reaction mixture is poured onto water (600 ml) and extracted with 1:1 ethyl acetate/diethyl ether (4×300 ml). The organic portions are washed with brine, dried (MgSO4) and concentrated in vacuo and the resulting crude is purified by chromatography on silica eluting with ethyl acetate/iso-hexane (1:8 increasing to 1:2) to yield the titled product. (MH+ 421)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08470848B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-0943b4dd7df54af2a12a73c866decbe3
출처 메모uspto-grants-2013_06