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HRID 2382009作成日:2026年10月26日

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

https://huagongshe.com/reaction/2382009

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Pyrrolo[3,2-b]pyridin-1-ylamineHCID 19601545—
反応物2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid chlorideHCID 87495795—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3-Fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid pyrrolo[3,2-b]pyridin-1-ylamideHCID 2509983224.3%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08258130B2
出典データセットuspto-grants-2012_09
ORD IDord-affce6f8a045483287bb1cbcbf6cdce8
出典メモuspto-grants-2012_09