HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910619Generated: October 31, 2026
4-Piperidinol, 1-methyl- → Methyl 4-[1-(1-methylpiperidin-4-yl)-2-oxo-1,2-dihydropyridin-3-yl]benzoate
https://huagongshe.com/reaction/910619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Piperidinol, 1-methyl- | HCID 66048 | — |
| Reactant | Cyanomethylenetrimethylphosphorane | HCID 11094579 | — |
| Reactant | Methyl 4-(2-oxo-1,2-dihydropyridin-3-yl)benzoate | HCID 53217923 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 4-[1-(1-methylpiperidin-4-yl)-2-oxo-1,2-dihydropyridin-3-yl]benzoate | HCID 57583942 | 18.9% |
Reaction Steps
Methyl 4-(2-oxo-1,2-dihydropyridin-3-yl)benzoate (316 mg) was suspended in toluene (7 mL), and 1-methyl-4-piperidinol (318 mg) and cyanomethylenetrimethylphosphorane (317 mg) were added thereto, followed by stirring at 100° C. for 1 hour. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methanol/chloroform=0% to 10%) to obtain methyl 4-[1-(1-methylpiperidin-4-yl)-2-oxo-1,2-dihydropyridin-3-yl]benzoate (85 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022208B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-7c156279b5404ed28763a85832a1d76a |
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| Source note | uspto-grants-2011_09 |
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