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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827120Generated: November 2, 2026

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

https://huagongshe.com/reaction/1827120

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyrimidineHCID 74404—
Reactant4-Methylbenzyl 4-(aminomethyl)1-piperidinecarboxylateHCID 16109417—
Product4-Methylbenzyl 4-[(2-pyrimidinylamino)methyl]-1-piperidinecarboxylateHCID 9881090—

Reaction Steps

The title compound was prepared as described in EXAMPLE 13, except using 4-methylbenzyl 4-(aminomethyl)-1-piperidinecarboxylate (300 mg, 1.14 mmol), 2-chloropyrimidine (131 mg, 1.14 mmol) as starting materials gave the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-7e8f4f9d7744453aaec15177a6d6529f
Source noteuspto-grants-2006_05