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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Chloro-6-methylpyrimidineHCID 581796—
ReactantHCID 86656722HCID 86656722—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-Methyl-1-(6-methylpyrimidin-4-yl)piperidin-4-amineHCID 5839804962%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-41653e35a10645528c9ee2deca4b3475
Source noteuspto-grants-2013_07