Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280764Generated: October 31, 2026

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

https://huagongshe.com/reaction/1280764

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 ml (109 mmol) 4-(1-diphenylmethylpiperidine-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 are distilled; thereby, sodium methylate precipitates and the temperature of the suspension increases to 102° C. under heavy foaming. The mixture is cooled to 70-80° C. and extracted twice with 45 ml and 30 ml of water. The organic phase is azeotropically dried on a moisture separator and cooled to ca. 0° C. The resulting precipitate is filtered off and crystallized from 190 ml toluol. Colorless crystals with a MP of 139° C. were recovered; yield: 46.3 g (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451816B1
Source datasetuspto-grants-2002_09
ORD IDord-eed79f641e81482ea4bb459f255846dd
Source noteuspto-grants-2002_09