HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451546Generated: October 26, 2026
Potassium Phosphate, Tribasic → 4-Methyl-1-(6-methylpyrimidin-4-yl)piperidin-4-amine
https://huagongshe.com/reaction/451546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 4-Chloro-6-methylpyrimidine | HCID 581796 | — |
| Reactant | HCID 86656722 | HCID 86656722 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-Methyl-1-(6-methylpyrimidin-4-yl)piperidin-4-amine | HCID 58398049 | 62% |
Reaction Steps
To a mixture of 4-methylpiperidin-4-amine bis(4-methylbenzenesulfonate) (3.91 g, 8.53 mmol) and 4-chloro-6-methylpyrimidine (1.10 g, 8.53 mmol) in NMP (35 mL) was added K3PO4 (3.12 g, 17.9 mmol) and the reaction mixture was stirred at 80° C. for 18 hours. After cooling to room temperature, 0.5 M aqueous K3PO4 was added and the mixture extracted twice with dichloromethane. The combined organic layers were extracted twice with HCl (1 N). The combined aqueous layers were made alkaline with NaOH (6 N), extracted twice with dichloromethane and the organic layers washed with brine, dried over sodium sulfate, filtered and evaporated. Purification by chromatography (silica gel, 70 g, 0 to 100% ethyl acetate in heptane; then 0 to 50% methanol in ethyl acetate, containing 10% triethylamine) afforded the title compound (1.09 g, 62%) as a light yellow semisolid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486967B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-41653e35a10645528c9ee2deca4b3475 |
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| Source note | uspto-grants-2013_07 |
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