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HRID 4324作成日:2026年10月23日

2-Aminopyridine → 2-(3,4-dimethoxyphenyl)-4H-pyrido[1,2-a]pyrimidin-4-one

https://huagongshe.com/ja/reaction/4324

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminopyridineHCID 10439—
反応物Ethyl 3,4-dimethoxybenzoylacetateHCID 2758465—
生成物2-(3,4-dimethoxyphenyl)-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 20152292150.8%

反応条件

温度100 °C

反応手順

Ethyl veratroylacetate (4.5 g) was added dropwise under stirring at 60°-70° C. to a suspension of 2-aminopyridine (0.84 g) in polyphosphoric acid (13.7 g). The reaction mixture was stirred at 100° C. for 3 hrs and poured into ice-water (50 ml). The aqueous solution was extracted with chloroform, washed with water, dried and evaporated to give dark oily residue which was chromatographed on silica gel using n-hexaneethyl acetate. The fractions were evaporated and the resulting residue was triturated with ethanol-isopropyl ether to give 2-(3,4-dimethoxyphenyl)-4-oxo-4H-pyrido[1,2-a]pyrimidine (3.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725600
出典データセットuspto-grants-1988_02
ORD IDord-5c3a5a99c48944198bf063c01ea01967
出典メモuspto-grants-1988_02