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HRID 1108077作成日:2026年10月26日

Methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate → Ethyl 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate

https://huagongshe.com/reaction/1108077

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylateHCID 11242202—
反応物1-(4-iodophenyl)-2-methyl-1H-imidazoleHCID 11289090—
反応物Sodium t-butoxideHCID 23676156—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
生成物Ethyl 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylateHCID 1115443160.9%

反応手順

A solution of methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate (1.04 g, 3.5 mmol), 4-(2-methylimidazol-1-yl)phenyliodide (0.89 g, 3.5 mmol), sodium t-butoxide (673 mg, 7 mmol) and tetrakis(triphenylphosphine)palladium (162 mg, 0.14 mmol) in dry ethanol (20 ml) was heated to reflux with stirring overnight. Volatiles were remeved by evaporation and the residue was partitioned between ethyl acetate (100 ml) and water (100 ml). The aqueous layer was extracted with ethyl acetate (100 ml). The combined organic layers were washed with brine (100 ml), dried (magnesium sulfat) and concentrated to dryness to give 1.09 g of crude product as a brown liquid. Purification by column chromatography (silica-gel, 50 g; methanol in dichloromethane, increasing the ratio of methanol from 0% to 4%) afforded the titled compound (0.90 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06063928
出典データセットuspto-grants-2000_05
ORD IDord-c8111a64e6d54f2191828c98f2bea4d2
出典メモuspto-grants-2000_05