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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 448733생성일: 2026년 10월 25일

Triethylamine → 1-[[(4-Benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester

https://huagongshe.com/reaction/448733

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물1-BenzoylpiperazineHCID 762654—
반응물Benzyl 1-aminocyclohexanecarboxylateHCID 15176238—
용매DichloromethaneHCID 6344—
생성물1-[[(4-Benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl esterHCID 5767291686.1%

반응 단계

A solution of 114 mg (0.9 mmol) of N,N-dimethylaminopyridine and 2.17 g (9.3 mmol) of 1-aminocyclohexanecarboxylic acid phenylmethyl ester in methylene chloride was added to a solution of 2.03 g (9.3 mmol) of di-t-butyl dicarbonate in 60 ml of methylene chloride, and the mixture was stirred at room temperature for 30 minutes. Thereafter, a solution of 1.88 g (18.6 mmol) of triethylamine and 1.86 g (9.8 mmol) of 1-(benzoyl)piperazine in methylene chloride was added, and the mixture was stirred at room temperature overnight. After the reaction solution was concentrated, the residue was dissolved in ethyl acetate, 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 diethyl ether to obtain 3.60 g (86%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481725B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-78457c1d0c144dc3a1667a7295654b83
출처 메모uspto-grants-2013_07