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HRID 872085作成日:2026年10月25日

Ethyl 3-(3-methoxyphenyl)-3-oxopropanoate → 3-(4-methylphenyl)-7-(3-methoxyphenyl)-2-methylpyrazolo[1,5-a]pyrimidin-5(4H)-one

https://huagongshe.com/reaction/872085

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 3-(3-methoxyphenyl)-3-oxopropanoateHCID 2759696—
反応物HCID 178423836HCID 178423836—
溶媒PyridineHCID 1049—
生成物3-(4-methylphenyl)-7-(3-methoxyphenyl)-2-methylpyrazolo[1,5-a]pyrimidin-5(4H)-oneHCID 136409077—

反応手順

3-Methyl-4-(4-methylphenyl)-1H-pyrazol-5-amine and ethyl 3-(3-methoxyphenyl)-3-oxopropanoate are stirred overnight in a pyridine (10 mL) solvent at 95° C. After cooling to room temperature, the reaction solvent is removed by distillation under reduced pressure. The remainder is extracted with ethyl acetate and water. The extracted organic layer is washed with brine and dehydrated with anhydrous MgSO4. The dehydrated organic layer is distilled under reduced pressure and the target compound is yielded by column chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08975264B2
出典データセットuspto-grants-2015_03
ORD IDord-2216046163e0473094b17b94538839bb
出典メモuspto-grants-2015_03