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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224863Generated: October 30, 2026

Sodium ethoxide → 2-[2-(2-Thienylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidone

https://huagongshe.com/reaction/224863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantN-{6-Oxo-5-[(pyridin-3-yl)methyl]-1,6-dihydropyrimidin-2-yl}nitramideHCID 12788688—
Reactant2-(2-Thienylmethylthio)ethylamine hydrochlorideHCID 13505310—
SolventEthanolHCID 702—
Product2-[2-(2-Thienylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidoneHCID 13505296—

Reaction Steps

2-(2-Thienylmethylthio)ethylamine hydrochloride (2 g) in ethanol (25 ml) was added to a solution of sodium ethoxide (prepared from 0.218 g sodium) in ethanol and the mixture was stirred for 0.5 hour. 2-Nitroamino-5-(3-pyridylmethyl)-4-pyrimidone (2.34 g) was added and the mixture was boiled under reflux for 40 hours and evaporated to dryness. Pyridine (50 ml) was added to the residue and the mixture was boiled under reflux for 24 hours and evaporated. The residue was crystallised from ethanol/ethyl acetate and further purified by elution from a column of silica gel with ethyl acetate/methanol (5:1) and recrystallisation from 2-propanol to give 2-[2-(2-thienylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidone m.p. 145°-148°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04234588
Source datasetuspto-grants-1980_11
ORD IDord-7e15a2672d9a47b889893898c89181c7
Source noteuspto-grants-1980_11