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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710843Generated: November 2, 2026

2-(4-Methoxybenzylamino)-5-(2-methylthioethoxy)pyrimidine → 5-(2-(Methylthio)ethoxy)pyrimidin-2-amine

https://huagongshe.com/reaction/1710843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Methoxybenzylamino)-5-(2-methylthioethoxy)pyrimidineHCID 58339649—
SolventTrifluoroacetic acidHCID 6422—
Product5-(2-(Methylthio)ethoxy)pyrimidin-2-amineHCID 5833965332.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-(4-Methoxybenzyl)-5-[2-(methylthio)ethoxy]pyrimidin-2-amine (172.4 mg) was dissolved in trifluoroacetic acid (3 mL) at room temperature, and the solution was stirred at 60° C. for 2.5 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was purified by preparative silica gel thin layer chromatography (chloroform:methanol=15:1) to obtain 5-[2-(methylthio)ethoxy]pyrimidin-2-amine (34 mg, 18% in 2 steps) as colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790737B2
Source datasetuspto-grants-2010_09
ORD IDord-b470deb22d0f4137af6aa772539fd902
Source noteuspto-grants-2010_09