戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 69934作成日:2026年10月24日

Sodium ethoxide → 5-Bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid

https://huagongshe.com/ja/reaction/69934

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ethoxideHCID 2723922—
反応物Mucobromic AcidHCID 3033972—
反応物2,6-Difluorobenzamidine hydrochlorideHCID 46318424—
溶媒EthanolHCID 702—
生成物5-Bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acidHCID 66652334—

反応手順

A 2.68 M NaOEt in EtOH solution (3 eq) was added to an ice-bath cooled mixture of 2,6-difluorobenzimidamide hydrochloride (2 eq) in EtOH (0.1 M). The resulting mixture was allowed to warm to rt and stirred under N2 for 30 min. To the reaction mixture was added drop wise a solution of mucobromic acid (1 eq) in EtOH and the reaction was heated in a 50° C. oil bath for 2.5 hr. After cooling to rt the reaction mixture was concentrated in vacuo. H2O and 1.0 N NaOH were added and the aqueous mixture was washed with EtOAc. The aqueous phase was acidified to pH=4 with 1.0 N HCl then extracted with EtOAc. Combined organic extracts were washed once with brine, then dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give 5-bromo-2-(2,6-difluorophenyl)pyrimidine-4-carboxylic acid. The crude product was used for the next step without further purification. LC/MS (m/z): 316.9 (MH+). LC: Rt: 2.426 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822497B2
出典データセットuspto-grants-2014_09
ORD IDord-cc678ab9ee294ee5b54fe1b9dddb6206
出典メモuspto-grants-2014_09