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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178399Generated: November 4, 2026

Methyl 3-(pyridin-3-yl)propanoate → N-[4-(1-diphenylmethylpiperidin-4-yl)-butyl]-3-(pyridin-3-yl)-propionamide

https://huagongshe.com/reaction/1178399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-(pyridin-3-yl)propanoateHCID 10329646—
ReactantSodium MethoxideHCID 10942334—
Reactant4-(1-Diphenylmethylpiperidine-4-yl)butylamineHCID 11034635—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductN-[4-(1-diphenylmethylpiperidin-4-yl)-butyl]-3-(pyridin-3-yl)-propionamideHCID 9846838—

Reaction Conditions

Temperature102 °C

Reaction Steps

21.6 g (131 mmol) 3-(3-pyridyl)-propionic acid methyl ester, 35.1 g (109 mmol) 4-(1-diphenylmethyl-piperidin-4-yl)-butylamine and 9.8 g (54.5 mmol) 30% sodium methylate solution in methanol are heated to boiling in 480 ml toluene for five hours. Subsequently, 30 ml of solvent is distilled off, sodium methylate precipitates thereby, and the temperature of the suspension increases under heavy foaming to 102° C. The mixture is cooled to 70-80° C. and extracted twice with 45 ml and 30 ml water. The organic phase is azeotropically dried in a moisture separator and cooled to ca. 0° C. The resulting precipitate is filtered and crystallized from 190 ml toluene. Colorless crystals with an MP of 139° C.; yield 46.3 g (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276524B2
Source datasetuspto-grants-2007_10
ORD IDord-89c350a21c674d2bb7c23358289c6e63
Source noteuspto-grants-2007_10