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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351483Generated: November 1, 2026

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

https://huagongshe.com/reaction/1351483

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 numberUS07217716B2
Source datasetuspto-grants-2007_05
ORD IDord-20c781d4e9204bb4a1ea8a677db75a70
Source noteuspto-grants-2007_05