戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 714929作成日:2026年10月26日

2,6-Difluorobenzaldehyde → ethyl 2-(2,6-difluorophenyl)-4-(pyridin-2-yl)-1H-imidazole-5-carboxylate

https://huagongshe.com/reaction/714929

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-DifluorobenzaldehydeHCID 136284—
反応物Ammonium AcetateHCID 517165—
反応物HCID 178472895HCID 178472895—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物ethyl 2-(2,6-difluorophenyl)-4-(pyridin-2-yl)-1H-imidazole-5-carboxylateHCID 595874977%

反応条件

温度160 °C

反応手順

A mixture of ethyl 2-(hydroxyimino)-3-oxo-3-(pyridin-2-yl)propanoate (0.300 g, 1.4 mmol), ammonium acetate (0.104 g, 1.4 mmol) and 2,6-difluorobenzaldehyde (0.145 mL, 1.3 mmol) in acetic acid (6 mL) was heated in the microwave at 160° C. for 2 minutes. The reaction mixture was diluted with MeOH and purified by SPE using a MP-TsOH resin cartridge (2500 mg). The crude mixture obtained was purified by preparative HPLC to afford ethyl 2-(2,6-difluorophenyl)-4-(pyridin-2-yl)-1H-imidazole-5-carboxylate (0.029 g, 0.09 mmol, 7%) as a pale solid. LCMS (2) Rt: 2.46 min; m/z (ES+) 330.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187465B2
出典データセットuspto-grants-2015_11
ORD IDord-ff96ec37b3dc4e8baf3423ead1d2c85e
出典メモuspto-grants-2015_11