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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2382009생성일: 2026년 10월 26일

Potassium Carbonate → 2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid pyrrolo[3,2-b]pyridin-1-ylamide

https://huagongshe.com/reaction/2382009

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Pyrrolo[3,2-b]pyridin-1-ylamineHCID 19601545—
반응물2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid chlorideHCID 87495795—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid pyrrolo[3,2-b]pyridin-1-ylamideHCID 2509983224.3%

반응 단계

A solution of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid chloride (0.45 mmol) in EtOAc (8 mL) is added to a stirred solution of pyrrolo[3,2-b]pyridin-1-ylamine (0.45 mmol) and potassium carbonate (0.45 mmol) in EtOAc (4 mL) and H2O (8 mL) at rt and the reaction mixture is stirred at rt overnight. EtOAc is evaporated in vacuo, and the resulting solid is collected by filtration. The solid is purified by silica gel chromatography eluting with 20-80% EtOAc in heptane to afford 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid pyrrolo[3,2-b]pyridin-1-ylamide (38 mg, 24%) as a solid. MS: 348 (M+H); 1H NMR (300 MHz, CDCl3): δ 2.76 (s, 3H), 6.59 (m, H) 7.07-7.64 (m, 4H), 7.96 (m, H), 8.23 (m, H), 8.32 (m, 2H), 9.12 (s, H), 10.01 (br, N—H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08258130B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-affce6f8a045483287bb1cbcbf6cdce8
출처 메모uspto-grants-2012_09