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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-(pyridin-3-yl)propanoate | HCID 10329646 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-(1-Diphenylmethylpiperidine-4-yl)butylamine | HCID 11034635 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[4-(1-diphenylmethylpiperidin-4-yl)-butyl]-3-(pyridin-3-yl)-propionamide | HCID 9846838 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07276524B2 |
|---|
| Source dataset | uspto-grants-2007_10 |
|---|
| ORD ID | ord-89c350a21c674d2bb7c23358289c6e63 |
|---|
| Source note | uspto-grants-2007_10 |
|---|