Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827122Generated: October 31, 2026

4-Chloro-2-methylthiopyrimidine → 4-Methylbenzyl 4-({[2-(methylsulfanyl)-4-pyrimidinyl]amino}methyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/1827122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-methylthiopyrimidineHCID 97113—
Reactant4-Methylbenzyl 4-(aminomethyl)1-piperidinecarboxylateHCID 16109417—
Product4-Methylbenzyl 4-({[2-(methylsulfanyl)-4-pyrimidinyl]amino}methyl)-1-piperidinecarboxylateHCID 10134767—

Reaction Steps

The title compound was prepared as described in EXAMPLE 13, except using 4-methylbenzyl 4-(aminomethyl)-1-piperidinecarboxylate (600 mg, 2.29 mmol), and 4-chloro-2-methylthiopyrimidine (386 mg, 2.40 mmol) as starting materials and 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-0f82f1b2a8e74627b75962cb823e8a4d
Source noteuspto-grants-2006_05