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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454133Generated: October 25, 2026

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

https://huagongshe.com/reaction/1454133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Pyridin-3-yl)propanoic acidHCID 259624—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantPiperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 12020263—
SolventDichloromethaneHCID 6344—
Product1-(3-Pyridin-3-yl-propionyl)-piperidine-3-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 1872748867.6%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476680B2
Source datasetuspto-grants-2009_01
ORD IDord-241f2e225f2f430cb0566e3092a14674
Source noteuspto-grants-2009_01