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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720881생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/720881

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 번호US07135483B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-951642434497462887d1203c1171c219
출처 메모uspto-grants-2006_11