戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 241413作成日:2026年10月25日

Sodium Carbonate → 3-(1H-imidazo[4,5-b]pyridin-2-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamine

https://huagongshe.com/reaction/241413

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
反応物5-bromo-3-(1H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-ylamineHCID 66869810—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物3-(1H-imidazo[4,5-b]pyridin-2-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamineHCID 66898551—

反応手順

58 mg (0.200 mmol) of 5-bromo-3-(1H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-ylamine and 45.8 mg (0.220 mmol) of 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole are suspended in 2 ml of N,N-dimethylformamide in a nitrogen-filled microwave vessel, and 0.57 ml (1.142 mmol) of 2M sodium carbonate solution and 23.1 mg (0.020 mmol) of tetrakis(triphenylphosphine)palladium(0) are added. The reaction solution is irradiated with microwaves for 30 min at 120° C. in the Biotage SmithSynthesizer. The reaction mixture is evaporated to dryness, and the residue is purified by means of RP-HPLC, giving 3-(1H-imidazo[4,5-b]pyridin-2-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamine; HPLC-MS [M+H]+ 292.2;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08648201B2
出典データセットuspto-grants-2014_02
ORD IDord-a1ef29d4a7fb4ec281e9f0fd034bb37c
出典メモuspto-grants-2014_02