HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66685Generated: October 30, 2026
Potassium Iodide → 3-[2-(4-benzoyl-1-piperidinyl)ethyl]-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one
https://huagongshe.com/reaction/66685
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-(2-Chloroethyl)-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 817866 | — |
| Reactant | Phenyl(piperidin-4-yl)methanone hydrobromide | HCID 20530718 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 3-[2-(4-benzoyl-1-piperidinyl)ethyl]-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 13035910 | — |
Reaction Steps
A mixture of 5.6 parts of 3-(2-chloroethyl)-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one, 6 parts of phenyl(4-piperidinyl)-methanone hydrobromide, 8 parts of sodium carbonate, 0.1 parts of potassium iodide and 240 parts of 4-methyl-2-pentanone is stirred and refluxed for 24 hours using a water-separator. The reaction mixture is filtered hot over Hyflo and the filtrate is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of ethanol and 1,1'-oxybisethane, yielding 6 parts of 3-[2-(4-benzoyl-1-piperidinyl)ethyl]-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one; mp. 122.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04342870 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-f8d6d80ba41a4864a815f3d5a9a3c597 |
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| Source note | uspto-grants-1982_08 |
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