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
Participants
| Role | Name | HCID | Charge |
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| 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451816B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-eed79f641e81482ea4bb459f255846dd |
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| Source note | uspto-grants-2002_09 |
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