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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166702Generated: October 31, 2026

4-(((2-Aminoethyl)thio)methyl)-5-methylimidazole → HCID 13137369, compound

https://huagongshe.com/reaction/2166702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 665568—
ReactantHCID 13137349HCID 13137349—
SolventPyridineHCID 1049—
ProductHCID 13137369HCID 13137369—

Reaction Steps

A mixture of 2-(5-methyl-4-imidazolylmethylthio)ethylamine (1.37 g), 2-nitroamino-5-(6-dimethylaminomethyl-3-pyridylmethyl)-4-pyrimidone (2.28 g) in pyridine were heated under reflux for 22 hr. The pyridine (12 ml) was evaporated at reduced pressure yielding [2-(5-methyl-4-imidazolyl-methylthio)ethylamino]-5-(6-dimethylaminomethyl-3-pyridylmethyl)-4-pyrimidone as a brown oily residue washed with water by decantation. The residue was dissolved in dilute ethanolic hydrochloric acid and the excess of solvent evaporated at reduced pressure. The residue was recrystallised from methanol/dilute ethanolic hydrochloric acid and then twice from methanol/ethanol to yield the tetrahydrochloride (0.82 g) as a light buff solid m.p. 167°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04388317
Source datasetuspto-grants-1983_06
ORD IDord-a97e36f5930f4cd195796848c32c15fe
Source noteuspto-grants-1983_06