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HRID 68331作成日:2026年10月24日

Potassium Carbonate → 3-(6-methoxy-2-(methylthio)pyrimidin-4-yl)-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/ja/reaction/68331

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4-Chloro-6-methoxy-2-(methylthio)pyrimidineHCID 9836999—
反応物1-(Phenylsulfonyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrolo[2,3-b]pyridineHCID 45588137—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒dimethoxyethane N,N-dimethylformamideHCID 18463208—
生成物3-(6-methoxy-2-(methylthio)pyrimidin-4-yl)-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 66889055—

反応条件

温度85 °C

反応手順

A mixture of 4-chloro-6-methoxy-2-(methylthio)pyrimidine (10.2 g, 53.7 mmol), 1-(phenylsulfonyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine (18.8 g, 48.8 mmol), potassium carbonate (48.8 g, 98 mmol), and tetrakis(triphenylphosphine) palladium (2.26 g, 1.95 mmol) in 9/1 dimethoxyethane/N,N-dimethylformamide (200 mL) was evacuated under vacuum and refilled with nitrogen and heated at 85° C. for 20 minutes. The cooled mixture was filtered to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822446B2
出典データセットuspto-grants-2014_09
ORD IDord-4e5f20db325347d39a1b2b06759395aa
出典メモuspto-grants-2014_09