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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704428생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → N-(3,4,5-trimethoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamide

https://huagongshe.com/reaction/704428

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물3,4,5-TrimethoxyanilineHCID 32285—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(3,4,5-trimethoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamideHCID 1488159834.7%

반응 단계

A mixture of 630 mg of 2-(3-pyridyl)thiazolidine-4-carboxylic acid, 520 mg of 3,4,5-trimethoxyaniline, 650 mg of dicyclohexylcarbodiimide and 430 mg of 1-hydroxybenzotriazole in 8 ml of N,N-dimethylformamide was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, and the insoluble matter was filtered off. The filtrate was washed in sequence with aqueous sodium hydrogen carbonate, water and saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Purification of the residue by silica gel column chromatography (eluent: ethyl acetate) gave 370 mg of N-(3,4,5-trimethoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamide. This compound was dissolved in 10 ml of ethyl acetate, and 2 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 mg of N-(3,4,5-trimethoxyphenyl)-2-(3-pyridyl)thiazolidine-4-carboxamide dihydrochloride. Melting point 130°-132° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04987132
출처 데이터셋uspto-grants-1991_01
ORD IDord-fb09ffdbb1b343418f9ab5cda69671af
출처 메모uspto-grants-1991_01