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HRID 874409作成日:2026年10月25日

Methyl 2-aminopyridine-4-carboxylate → Methyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylate

https://huagongshe.com/reaction/874409

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2-aminopyridine-4-carboxylateHCID 236984—
反応物2-Bromo-1-(2,5-difluorophenyl)ethanoneHCID 2778264—
溶媒EthanolHCID 702—
生成物Methyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylateHCID 90383269135.9%

反応条件

温度60 °C

反応手順

2-Bromo-1-(2,5-difluorophenyl)ethanone (1.5 g) was added to an ethanol (8.2 ml) solution of methyl 2-aminoisonicotinate (1.0 g), and the obtained mixture was then stirred in a nitrogen atmosphere at 60° C. for 18 hours. Thereafter, 2-bromo-1-(2,5-difluorophenyl)ethanone (0.77 g) was added to the reaction solution, and the obtained mixture was then stirred for 6 hours at the same temperature as described above. Thereafter, the reaction solution was concentrated under reduced pressure, and ethyl acetate (10 ml) was then added to the obtained residue. The precipitated solid was collected by filtration, and it was washed with ethyl acetate (15 ml) and heptane (6 ml) and was then dried, so as to obtain the title compound (2.5 g) in the form of a pink solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08980889B2
出典データセットuspto-grants-2015_03
ORD IDord-4d7a312991604e409a51268762029261
出典メモuspto-grants-2015_03