関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Aminopyridine | HCID 10439 | — |
| 反応物 | Ethyl 3,4-dimethoxybenzoylacetate | HCID 2758465 | — |
| 生成物 | 2-(3,4-dimethoxyphenyl)-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 20152292 | 150.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04725600 |
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| 出典データセット | uspto-grants-1988_02 |
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| ORD ID | ord-5c3a5a99c48944198bf063c01ea01967 |
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| 出典メモ | uspto-grants-1988_02 |
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