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HRID 1934881作成日:2026年10月26日

Triethylamine → 6-Methyl-2-(4-methylphenyl)-alpha-oxo-imidazo[1,2-a]pyridine-3-acetic Acid Ethyl Ester

https://huagongshe.com/reaction/1934881

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium CarbonateHCID 10340—
反応物Phosphorus oxychlorideHCID 24813—
反応物6-Methyl-2-(4-methylphenyl)imidazo(1,2-a)pyridineHCID 667720—
反応物Ethanedioic acid, 1-ethyl ester, potassium salt (1:1)HCID 23678856—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物6-Methyl-2-(4-methylphenyl)-alpha-oxo-imidazo[1,2-a]pyridine-3-acetic Acid Ethyl EsterHCID 1116304997.5%

反応条件

温度10 °C

反応手順

A suspension of potassium monoethyl oxalate (84.3 g; 0.54 mols) in methylene chloride (395 mL) is added dropwise with phosphorous oxychloride (82.8 g; 0.54 mols) keeping the temperature at about 30° C. After 4÷6 hours, 2-(4-methylphenyl)-6-methylimidazo[1,2-a]-pyridine (100.0 g; 0.45 mols) is added, keeping the temperature below 35° C. The resulting suspension is added dropwise with triethylamine (50.5 g; 0.50 mols) keeping the mixture at the reflux temperature. After one hour under these conditions, the reaction mixture is cooled to 5÷10° C. and poured into a suspension of sodium carbonate (95 g; 0.89 mols) in water (500 mL) keeping the temperature below 35° C. The phases are separated and the upper aqueous phase is reextracted with methylene chloride (45 mL). The combined organic phases are washed with water (45 mL) and concentrated to a residue under vacuum. The solid residue is taken up in ethanol (590 mL), heated to dissolution and left to crystallize. After cooling to about 0° C. the solid is filtered, washed with ethanol and dried at 50° C. under vacuum to obtain ethyl 2-(4-methylphenyl)-6-methylimidazo[1,2-a]-pyridine-3-glyoxalate (141.5 g, 99.5% titre, 97.5% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06384226B2
出典データセットuspto-grants-2002_05
ORD IDord-6bb3a72d10644d1bb2b0ce6f5a1e9f72
出典メモuspto-grants-2002_05