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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704435생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → N-[p-(3-methylbutoxy)benzyl]-2-(3-pyridyl)thiazolidine-4-carboxamide

https://huagongshe.com/ko/reaction/704435

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
반응물4-(3-Methyl-butoxy)-benzylamineHCID 808425—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-[p-(3-methylbutoxy)benzyl]-2-(3-pyridyl)thiazolidine-4-carboxamideHCID 1530632597.6%

반응 단계

A mixture of 1.13 g of p-(3 methylbutoxy)benzylamine, 1.29 g of 2-(3-pyridyl)thiazolidine-4-carboxylic acid, 1.25 g of dicyclohexylcarbodiimide and 0.82 g of 1-hydroxybenzotriazole in 20 ml of N,N-dimethylformamide was stirred overnight at room temperature. The reaction mixture was diluted with 100 ml of ethyl acetate, and the insoluble matter was filtered off. The filtrate was washed in sequence with saturated aqueous solution of sodium hydrogen carbonate, water and saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure Purification of the thus-obtained residue by silica gel column chromatography (eluent: ethyl acetate) gave 2.20 g of N-[p-(3-methylbutoxy)benzyl]-2-(3-pyridyl)thiazolidine-4-carboxamide. To a solution of this compound in 60 ml of ethyl acetate was added 4 ml of 4N hydrogen chloride solution in dioxane. The precipitate solid was collected by filtration, washed with ethyl acetate and dried under reduced pressure to give 2.30 g of N-[p-(3-methylbutoxy)benzyl]-2-(3-pyridyl)thiazolidine-4-carboxamide dihydrochloride. Melting point 120°-128° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04987132
출처 데이터셋uspto-grants-1991_01
ORD IDord-e4529035614741248b3c2d5fb4b1f7cb
출처 메모uspto-grants-1991_01