戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1945592作成日:2026年10月26日

Chloroacetaldehyde → 5-Bromo-8-methylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1945592

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroacetaldehydeHCID 33—
反応物6-Bromo-3-methylpyridin-2-amineHCID 59605384—
生成物5-Bromo-8-methylimidazo[1,2-a]pyridineHCID 5960521695%

反応条件

温度100 °C

反応手順

A mixture of 6-bromo-3-methylpyridin-2-ylamine (359 mg, 1.92 mmol) and chloroacetaldehyde (1 mL, 50 wt. % in water) in IMS (4 mL) was stirred at 100° C. in a sealed tube for 1.5 hours, then cooled to room temperature and loaded onto an Isolute® SCX-2 cartridge (10 g). The cartridge was washed with MeOH then eluted with 2 M NH3 in MeOH to give 5-Bromo-8-methylimidazo[1,2-a]pyridine as a beige solid (387 mg, 95%). 1H NMR (400 MHz, CHCl3-d): δ 7.79 (d, J=1.3 Hz, 1 H); 7.69 (d, J=1.3 Hz, 1 H); 6.96 (d, J=7.3 Hz, 1 H); 6.91 (dq, J=7.3, 1.1 Hz, 1 H); 2.61 (d, J=1.1 Hz, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394796B2
出典データセットuspto-grants-2013_03
ORD IDord-e1725fbf5ede41ce9ec2d693abeb259e
出典メモuspto-grants-2013_03