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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704427생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/704427

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxyanilineHCID 10824—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(3-methoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamideHCID 1488159225.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04987132
출처 데이터셋uspto-grants-1991_01
ORD IDord-54cb1d8a97614a4bb5fb4d7cea319536
출처 메모uspto-grants-1991_01