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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445351Generated: October 26, 2026

Ethanol → 4-amino-4-methyl-N-(2-pyrimidinyl)piperidine

https://huagongshe.com/reaction/1445351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChloropyrimidineHCID 74404—
Reactant4-Methylpiperidin-4-amineHCID 21090445—
SolventWaterHCID 962—
Product4-amino-4-methyl-N-(2-pyrimidinyl)piperidineHCID 2188256665.1%

Reaction Steps

2 ml of an ethanol suspension containing 260 mg of 4-amino-4-methylpiperidine (synthesized according to a method described in U.S. Pat. No. 5,821,240), 237 mg of 2-chloropyrimidine and 858 mg of potassium carbonate was stirred at 50° C. for 12 hours. The reaction mixture was poured into water, and extracted with chloroform. The extract was washed with brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel flash column chromatography [solvent: chloroform-methanol-aqueous ammonia (300′:10:1)] to obtain 259 mg of 4-amino-4-methyl-N-(2-pyrimidinyl)piperidine (Reference Example 8-1 in Table 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666869B2
Source datasetuspto-grants-2010_02
ORD IDord-d7f8b4a72a26430a99b45e94d606649d
Source noteuspto-grants-2010_02