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HRID 73828作成日:2026年10月26日

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

https://huagongshe.com/reaction/73828

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Di-tert-butyl dicarbonateHCID 90495—
反応物1-BenzoylpiperazineHCID 762654—
反応物Benzyl 1-aminocyclohexanecarboxylateHCID 15176238—
溶媒DichloromethaneHCID 6344—
生成物1-[[(4-Benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl esterHCID 5767291686.1%

反応手順

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 thereto, 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829209B2
出典データセットuspto-grants-2014_09
ORD IDord-2922b66984ce4404a06faf19cb1dcefd
出典メモuspto-grants-2014_09