Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Fluorobenzoyl)piperidine | HCID 2724440 | — |
| Reactant | HCID 20254945 | HCID 20254945 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Prideperone | HCID 3050428 | — |
Reaction Steps
41.4 g (0.2 mol) of 4-(p-fluorobenzoyl)-piperidine are dissolved in 120 ml of dioxan, and 28.3 g (0.1 mol) of N-(2-bromoethyl)-5-cyano-2-methoxybenzamide are added and the whole is then stirred at room temperature for 60 hours. A solution of potassium carbonate is then added to the reaction mixture and the whole is then extracted with methylene chloride. The methylene chloride solution is washed neutral with water and concentrated in a water-jet vacuum. A light yellow crystalline product remains behind which is suspended in 200 ml of ethanol and stirred for 2 hours. The solid product is then filtered with suction and subsequently washed with 20 ml of ice-cold ethanol. 5-Cyano-N-[2-[4-(p-fluorobenzoyl)-piperidinyl]-ethyl]-2-methoxybenzamide is obtained in the filtration residue in the form of white powder of melting point 167°-169°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04559349 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-4c9e05bf2b1745a2b4e7a87d3d49e0aa |
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| Source note | uspto-grants-1985_12 |
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