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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1454133생성일: 2026년 10월 27일

Triethylamine → 1-(3-Pyridin-3-yl-propionyl)-piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/1454133

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-(Pyridin-3-yl)propanoic acidHCID 259624—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 12020263—
용매DichloromethaneHCID 6344—
생성물1-(3-Pyridin-3-yl-propionyl)-piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 1872748867.6%

반응 단계

Piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (13) (150 mg; 0.4 mmol) is dissolved in methylene chloride (10 mL) at ambient temperature. 3-Pyridinepropionic acid (60.0 mg; 0.4 mmol), triethylamine (0.111 mL; 0.4 mmol), and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.0836 g; 0.4 mmol) are added sequentially. The mixture is stirred for 18 hours at ambient temperature then diluted with methylene chloride (90 mL) and washed successively with water (40 mL), saturated aqueous sodium bicarbonate (40 mL), and saturated brine (25 mL). The organic layer is dried over MgSO4, filtered, and concentrated in vacuo. The residue is purified via silica gel chromatography with gradient elution (1%→20% methanol in methylene chloride) affording the desired product (138.4 mg) as an oil. ESMS: MH+ 512.4 (base).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07476680B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-241f2e225f2f430cb0566e3092a14674
출처 메모uspto-grants-2009_01