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HRID 555985作成日:2026年10月26日

2,4,6-Trimethylpyridine → (6-Bromo-imidazo[1,2-a]pyridin-2-yl)-carbamic acid phenyl ester

https://huagongshe.com/reaction/555985

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物Phenyl chloroformateHCID 15891—
反応物6-Bromoimidazo[1,2-a]pyridin-2-amineHCID 44119296—
溶媒TetrahydrofuranHCID 8028—
生成物(6-Bromo-imidazo[1,2-a]pyridin-2-yl)-carbamic acid phenyl esterHCID 59251768—

反応条件

温度0 °C

反応手順

To a solution of 6-bromo-imidazo[1,2-a]pyridin-2-ylamine (Intermediate A1)(6.2 g, 29.2 mmol) in THF (400 ml) is added 2,4,6-trimethylpyridine (5.8 ml, 43.9 mmol). The reaction mixture is cooled to 0° C. (ice-bath) and treated dropwise with a solution of phenyl chloroformate (3.85 ml, 30.7 mmol) in THF (50 ml) over 15 minutes. The reaction mixture is stirred overnight, at room temperature, quenched with water and stirred for a further 5 minutes resulting in a white precipitate. The solid is collected by filtration and dried under vacuum (40° C.) overnight to afford the title compound [MH+ 331.99 and 333.99].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053574B2
出典データセットuspto-grants-2011_11
ORD IDord-d2967969602f4d4daaba04f8a599af03
出典メモuspto-grants-2011_11