돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704429생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → N-nonadecyl-2-(3-pyridyl)thiazolidine-4-carboxamide

https://huagongshe.com/reaction/704429

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1-AminononadecaneHCID 106416—
반응물2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N-nonadecyl-2-(3-pyridyl)thiazolidine-4-carboxamideHCID 1488155421.9%

반응 단계

A solution of 500 mg of dicyclohexylcarbodiimide in 3 ml of tetrahydrofuran was added dropwise to a mixture of 510 mg of 2-(3-pyridyl)thiazolidine-4-carboxylic acid, 490 mg of 1-hydroxybenzotriazole, 680 mg of nonadecylamine and 12 ml of tetrahydrofuran with ice cooling, and the resulting mixture was stirred with ice cooling for 1 hour and then at room temperature for 12 hours. The reaction mixture was diluted with 30 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 sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate) and recrystallized from ethyl acetate to give 250 mg of N-nonadecyl-2-(3-pyridyl)thiazolidine-4-carboxamide. Melting point 108°-110° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04987132
출처 데이터셋uspto-grants-1991_01
ORD IDord-b33b29cc6a4b49c7b2dfc0cdad0ca94c
출처 메모uspto-grants-1991_01