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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220203생성일: 2026년 10월 25일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3-(2-Phenyl-piperidine-1-carbonyl)-piperidine-1-carboxlic acid tert.-butyl ester

https://huagongshe.com/reaction/220203

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물2-PhenylpiperidineHCID 103020—
반응물1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 2735647—
용매dichloromethane N,N-dimethylformamideHCID 22350042—
용매Sodium chloride; waterHCID 57417360—
생성물3-(2-Phenyl-piperidine-1-carbonyl)-piperidine-1-carboxlic acid tert.-butyl esterHCID 5782231031.1%

반응 단계

To a solution of 2 g of 1-(tert-butoxycarbonyl)-3-piperidinecarboxylic acid (commercially available) (8.72 mmol) in 15 mL of DMF: DCM (3:1) was added 1.39 g 2-phenylpiperidine (commercially available) (8.72 mmol) and 3.04 mL DIPEA (17.4 mmol). The mixture was stirred at room temperature for 10 minutes. 2.5 g EDCI (13.1 mmol) and 2.04 g HOBT (13.1 mmol) was added. The mixture was stirred for 6 h at room temperature, diluted with brine (50 mL) and extracted with ethyl acetate (2×40 mL). The combined organic layers were dried over sodium sulfate, filtered and evaporated at reduced pressure to obtain the crude product, which was further purified by column chromatography on silica eluting with 30-35% ethyl acetate in hexane to yield 1 g (31%) of the title compound. (MH+) 372.18.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202888B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-b663db6a751e4092b02db1302cc23275
출처 메모uspto-grants-2012_06