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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1627439생성일: 2026년 10월 24일

Triethylamine → 1-[(3-Furanylcarbonyl)amino]cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/ko/reaction/1627439

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Furoic acidHCID 10268—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Methyl 1-aminocyclohexane-1-carboxylate hydrochlorideHCID 22645079—
용매DichloromethaneHCID 6344—
생성물1-[(3-Furanylcarbonyl)amino]cyclohexanecarboxylic acid methyl esterHCID 3247401091%

반응 단계

105 g (550 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added to a solution of 98.8 g (500 mmol) of 1-aminocyclohexanecarboxylic acid methyl ester hydrochloride, 84.2 g (550 mmol) of 1-hydroxybenzotriazole, 56.0 g (500 mmol) of 3-furancarboxylic acid and 152 g (1.5 mol) of triethylamine in 1000 ml of methylene chloride under ice-cooling. After the mixture was stirred at room temperature overnight, the reaction solution was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the mixture was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, the obtained crystal was washed with diisopropyl ether to obtain 114 g (91%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785631B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-6c37fe921e314f89b791b2d18d4da163
출처 메모uspto-grants-2014_07