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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1042259생성일: 2026년 10월 26일

Sodium Carbonate → 4-(2-fluoropyridin-3-yl)-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1042259

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Fluoropyridine-3-boronic acidHCID 2783270—
반응물7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-(2-fluoropyridin-3-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 5962737017%

반응 단계

A mixture of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (7.68 g, 50 mmol), 2-fluoropyridin-3-ylboronic acid (10.57 g, 75 mmol), and tetrakis(triphenylphosphine)palladium(0) (2.89 g, 2.5 mmol) was suspended in DME (300 mL) and aqueous sodium carbonate (10%) (50 mL, 100 mmol). The suspension was heated at reflux over night, cooled to r.t. and the reaction mixture was partitioned between EtOAc (300 mL) and NaHCO3 (aq., sat., 200 mL). The aqueous layer was washed with EtOAc twice. The organic layers were combined and washed with brine, then loaded on silica and purified via flash column (EtOAc:hexane=50-95%) on ISCO to give 4-(2-fluoropyridin-3-yl)-7H-pyrrolo[2,3-d]pyrimidine as a light yellow solid with a green tint (1.85 g, 17% yield). MS (ESI, pos. ion) m/z: 214 [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08557830B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-f56f02f51a004aaa8565503a101a2944
출처 메모uspto-grants-2013_10