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HRID 704427作成日:2026年10月26日

3-Methoxyaniline → N-(3-methoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamide

https://huagongshe.com/reaction/704427

反応式

関与物質

役割名称HCID仕込み量
反応物3-MethoxyanilineHCID 10824—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-(3-methoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamideHCID 1488159225.7%

反応手順

A mixture of 630 mg of 2-(3-pyridyl)thiazolidine-4-carboxylic acid, 350 mg of m-anisidine, 650 mg of dicyclohexylcarbodiimide and 430 mg of 1-hydroxybenzotriazole in 8 ml of dimethylformamide was stirred overnight at room temperature. The reaction mixture was diluted with 50 ml of ethyl acetate, and the insoluble matter was filtered off. The filtrate was washed with two portions of water, and then with aqueous solution of sodium hydrogen carbonate, water and saturated aqueous solution of sodium chloride in that order, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue thus obtained was purified by preparative thin layer chromatography to give 230 mg of N-(3-methoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamide. This compound was dissolved in ethyl acetate, and 1 ml of 2N hydrogen chloride solution in dioxane was added. The resultant solid was collected by filtration, washed with ethyl acetate and dried to give 250 mg of N-(3-methoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamide dihydrochloride. Melting point 129° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04987132
出典データセットuspto-grants-1991_01
ORD IDord-54cb1d8a97614a4bb5fb4d7cea319536
出典メモuspto-grants-1991_01