Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1904938생성일: 2026년 10월 26일
Thionyl Chloride → 3-ethoxycarbonyl-9-(4-ethoxycarbonylbenzoyl)thio-4H-pyrido[1,2-a]pyrimidin-4-one
https://huagongshe.com/reaction/1904938
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | Monoethyl terephthalate | HCID 164720 | — |
| 반응물 | 3-ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 14306471 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 3-ethoxycarbonyl-9-(4-ethoxycarbonylbenzoyl)thio-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 14306444 | 105.5% |
반응 단계
To a mixture of 1.47 g (2.4 mmol) of 4-ethoxycarbonylbenzoic acid, 3 drops of DMF and 10 ml of benzene is added 0.52 g (4.4 mmol) of thionyl chloride, and the resultant mixture is refluxed for 3 hours under stirring and concentrated in vacuo to dryness. The residue is dissolved in acetone and mixed with 1.4 g of solid potassium carbonate and then 0.5 g (2 mmol) of 3ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-one II-1, and the resultant mixture is vigorously stirred at room temperature for 20 minutes. The reaction mixture is concentrated in vacuo to dryness, and the residue is distributed in chloroformwater. The organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is chromatographed on a column of silica gel, which is eluted with ethyl acetate to give 0.9 g of the titled compound Ie-56.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04840953 |
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| 출처 데이터셋 | uspto-grants-1989_06 |
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| ORD ID | ord-f6fbb70c6e3c49548a244d6c0192a6d7 |
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| 출처 메모 | uspto-grants-1989_06 |
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