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HRID 1449461作成日:2026年10月27日

Triethylamine → diethyl 3-(m-chlorophenyl)-4-methyl-2-oxo-2H-pyrano[2,3-b]pyridine-6,7-dicarboxylate

https://huagongshe.com/reaction/1449461

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ammonium HydroxideHCID 14923—
反応物3-Chlorophenylacetic acidHCID 15879—
反応物Diethyl 5-acetyl-1,6-dihydro-6-oxo-2,3-pyridinedicarboxylateHCID 13752508—
溶媒Acetic AnhydrideHCID 7918—
生成物diethyl 3-(m-chlorophenyl)-4-methyl-2-oxo-2H-pyrano[2,3-b]pyridine-6,7-dicarboxylateHCID 1995819795.1%

反応手順

Diethyl 5-acetyl-1,6-dihydro-6-oxo-2,3-pyridinedicarboxylate (12.0 g, 0.043 mol), 3-chlorophenyl acetic acid (7.33 g, 0.043 mol) and triethylamine (6.52 g) are refluxed in 120 mL of acetic anhydride for three hours. The reaction mixture is cooled, poured into 120 mL of ice-cold water and made alkaline to pH 8 with an ammonium hydroxide solution. The crystalline solid is filtered and washed with water to give (17.0 g, 95%) of the product after drying. Recrystallization from ethyl acetate affords the pure product (13.29, 74% yield), melting point 170°-172° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05599772
出典データセットuspto-grants-1997_02
ORD IDord-fdbe5ec1280b4276857d2f6d2774c78e
出典メモuspto-grants-1997_02