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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

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물Monoethyl terephthalateHCID 164720—
반응물3-ethoxycarbonyl-9-mercapto-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 14306471—
촉매DimethylformamideHCID 6228—
용매BenzeneHCID 241—
생성물3-ethoxycarbonyl-9-(4-ethoxycarbonylbenzoyl)thio-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 14306444105.5%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04840953
출처 데이터셋uspto-grants-1989_06
ORD IDord-f6fbb70c6e3c49548a244d6c0192a6d7
출처 메모uspto-grants-1989_06