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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729201Generated: October 30, 2026

3-Methylpiperidine → HCID 23371661, compound

https://huagongshe.com/reaction/1729201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylpiperidineHCID 79081—
Reactant4-Chloro-N,6-dimethyl-1,3,5-triazin-2-amineHCID 12237262—
SolventAcetoneHCID 180—
ProductHCID 23371661HCID 2337166141.3%

Reaction Steps

A mixture of 4-chloro-2-methyl-6-methylamino-1,3,5-triazine (1.06 g; 6.7 mM; described in J. Pharm. Soc. (Japan) 1975, 95, p.512) and 3-methylpiperidine (1.32 g, 13.3 mM) in acetone (10 ml) was stirred at ambient temperature for 6 hours. The mixture was filtered and the solid was partitioned between 3N aqueous ammonia solution (50 ml) and dichloromethane (50 ml). The organic solution was separated and dried (MgSO4) and the solvent was removed, and the residue was crystallised from elthanol. There was thus obtained 2-methyl-6-methylamino-4-(3-methylpiperidino)-1,3,5-triazine (608 mg, 41.3% yield) m.p. 155°-155.50° C.; microanalysis found: C,59.9; H,8.7; N,31.6%; C11H19N5 requires C,59.7; H,8.6; N,31.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332737
Source datasetuspto-grants-1994_07
ORD IDord-5df69f49255d422b983023f46bcc16b6
Source noteuspto-grants-1994_07