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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127205Generated: October 30, 2026

2-Nitroamino-5-(2-methoxy-4-pyridyl)methyl-4-pyrimidone → 2-[2-(3-Bromo-2-pyridylmethylthio)ethylamino]-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidone

https://huagongshe.com/reaction/127205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitroamino-5-(2-methoxy-4-pyridyl)methyl-4-pyrimidoneHCID 12783833—
Reactant2-{[(3-Bromopyridin-2-yl)methyl]sulfanyl}ethan-1-amineHCID 12951527—
SolventEthanolHCID 702—
Product2-[2-(3-Bromo-2-pyridylmethylthio)ethylamino]-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidoneHCID 12788675—

Reaction Steps

Reaction of 2-(3-bromo-2-pyridylmethylthio)ethylamine with 1.15 molar equivalents of 2-nitroamino-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidone in refluxing ethanol for 18 hours gave 2-[2-(3-bromo-2-pyridylmethylthio)ethylamino]-5-(2-methoxy-4-pyridylmethyl)-4-pyrimidone m.p. 70-72° which was boiled under reflux in ethanol containing hydrogen chloride to give 2-[2-(3-bromo-2-pyridylmethylthio) ethylamino]-5-(2-hydroxy-4-pyridylmethyl)-4-pyrimidone trihydrochloride, m.p. 195-198.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255428
Source datasetuspto-grants-1981_03
ORD IDord-8a2f7444ab1f4d0a85dcc7436c55a7c4
Source noteuspto-grants-1981_03