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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351484Generated: October 26, 2026

2-Chloro-5-methylpyrimidine → Benzyl 4-{[(5-methyl-2-pyrimidinyl)amino]methyl}-1-piperidinecarboxylate

https://huagongshe.com/reaction/1351484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-methylpyrimidineHCID 581719—
Reactant4-Aminomethyl-1-N-Cbz-piperidineHCID 21955499—
ProductBenzyl 4-{[(5-methyl-2-pyrimidinyl)amino]methyl}-1-piperidinecarboxylateHCID 9881091—

Reaction Steps

The title compound was prepared as described in EXAMPLE 13, except using benzyl 4-(aminomethyl)-1-piperidinecarboxylate (298 mg, 1.20 mmol), 2-chloro-5-methylpyrimidine (EXAMPLE 144, Step 1) (51 mg, 0.40 mmol) as starting materials and using no solvent and 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-8b7db9672cf845399e7a2878e6aaa7e3
Source noteuspto-grants-2007_05