戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1044013作成日:2026年10月25日

Potassium tert-butoxide → 5-chloro-2-(1-methylcyclopropyl)-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/1044013

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium tert-butoxideHCID 23665647—
反応物6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amineHCID 57908192—
溶媒DimethylformamideHCID 6228—
生成物5-chloro-2-(1-methylcyclopropyl)-1H-pyrrolo[2,3-c]pyridineHCID 5790817573%

反応条件

温度80 °C

反応手順

To a solution of 6-chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine (3.0 g, 15 mmol) in DMF (50 mL) was added t-BuOK (3.3 g, 29 mmol) under N2 atmosphere. The mixture was heated at 80° C. overnight and quenched with H2O (100 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (50 mL×3). The combined organic layer was washed with brine, dried over anhydrous Na2SO4 and purified by chromatography on silica gel (3% EtOAc in petroleum ether) to afford 5-chloro-2-(1-methylcyclopropyl)-1H-pyrrolo[2,3-c]pyridine (2.2 g, 73%). 1H-NMR (CDCl3, 300 MHz) δ 9.79 (br s, 1H), 8.37 (s, 1H), 7.36 (s, 1H), 6.16 (s, 1H), 1.51 (s, 3H), 1.09 (m, 2H), 0.89 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563573B2
出典データセットuspto-grants-2013_10
ORD IDord-c5723815144547c3a710d8476f6c9db9
出典メモuspto-grants-2013_10