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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827174Generated: October 31, 2026

Triethylamine → 4-Methylbenzyl 4-[(2-pyrimidinylamino)methyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1827174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-ChloropyrimidineHCID 74404—
Reactant4-Methylbenzyl 4-(aminomethyl)1-piperidinecarboxylateHCID 16109417—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Methylbenzyl 4-[(2-pyrimidinylamino)methyl]-1-piperidinecarboxylateHCID 9881090—

Reaction Steps

A stirred solution of 4-methylbenzyl 4-(aminomethyl)-1-piperidinecarboxylate (INTERMEDIATE 2A) (20.00 g, 76.23 mmol), 2-chloro-pyrimidine (8.73 g, 76.23 mmol) and triethylamine (21.25 mL, 152.46 mmol) in DMF (40 mL) was heated at 100° C. for 6 h. The reaction solution was cooled to rt, then diluted with ethyl acetate (800 mL), washed with sat. aq. NaHCO3 (100 mL), water (3×100 mL), brine (100 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography (CH2Cl2/IPA/hexanes) to give 4-methylbenzyl 4-[(2-pyrimidinylamino)methyl]-1-piperidinecarboxylate. M.S.(M+1): 341.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-f6e00a4435814afbb32ce1e01f3bc286
Source noteuspto-grants-2006_05