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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719536Generated: November 3, 2026

4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole → 2-[2-(5-Methyl-4-imidazolylmethylthio)ethylamino]-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one

https://huagongshe.com/reaction/1719536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 665568—
Reactant2-Nitroamino-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-oneHCID 70354123—
SolventEthanolHCID 702—
Product2-[2-(5-Methyl-4-imidazolylmethylthio)ethylamino]-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-oneHCID 7035394655.5%

Reaction Steps

2-(5-Methyl-4-imidazolylmethylthio)ethylamine (1.37 g) and 2-nitroamino-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one (2.08 g) were refluxed in ethanol (10 ml) for 24 hours. The reaction mixture was cooled and evaporated under reduced pressure to afford a glassy residue which was washed with hot water yielding a white solid. This solid was filtered off, washed with water and recrystallised from methanol to yield 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-5-(1-methyl-2-oxopyridin-4-ylmethyl)pyrimidin-4-one (1.61 g); recrystallisation from aqueous methanol afforded the title compound, m.p. 202.5°-203.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04540699
Source datasetuspto-grants-1985_09
ORD IDord-864a287d8d434674aac02d611e871574
Source noteuspto-grants-1985_09