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HRID 44615作成日:2026年10月23日

Ethyl benzoylformate → 1-[2-(Benzylthio)-8-oxo-5,6,7,8-tetrahydroquinazolin-7-yl]-2-phenylethane-1,2-dione

https://huagongshe.com/ja/reaction/44615

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl benzoylformateHCID 15349—
反応物Sodium hydrideHCID 24758—
反応物2-(benzylthio)-6,7-dihydroquinazolin-8(5H)-oneHCID 57444113—
溶媒TetrahydrofuranHCID 8028—
生成物1-[2-(Benzylthio)-8-oxo-5,6,7,8-tetrahydroquinazolin-7-yl]-2-phenylethane-1,2-dioneHCID 5744411468%

反応手順

To a solution of 0.22 g (0.81 mmol) of 2-(benzylthio)-6,7-dihydroquinazolin-8(5H)-one in 5 mL of dry tetrahydrofuran cooled to −50° C., 0.10 g of sodium hydride 60% in mineral oil were added. The resulting suspension was maintained at the same temperature for 30 minutes and then 0.59 mL of ethyl α-oxobenzeneacetate (PhCOCOOEt) were added and the reaction mixture allowed to come to room temperature. After 16 hours the mixture was partitioned between water and ethyl acetate and the organic layer was dried over Na2SO4 and evaporated to dryness. The residue was purified by chromatography on a silica gel column (eluant hexane/ethyl acetate 7/3) giving 0.22 g (68% yield) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541429B2
出典データセットuspto-grants-2013_09
ORD IDord-6cb9fd63185241d28ffc6683e788d26e
出典メモuspto-grants-2013_09