Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224855Generated: October 29, 2026

5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine → 2-[2-(5-Dimethylaminomethyl-2-furylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidone

https://huagongshe.com/reaction/224855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamineHCID 162203—
ReactantN-{6-Oxo-5-[(pyridin-3-yl)methyl]-1,6-dihydropyrimidin-2-yl}nitramideHCID 12788688—
SolventEthanolHCID 702—
Product2-[2-(5-Dimethylaminomethyl-2-furylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidoneHCID 13505287—

Reaction Steps

A solution of 2-(5-dimethylaminomethyl-2-furyl-methylthio)ethylamine (2.25 g, 0.105 mol) and 2-nitroamino-5-(3-pyridylmethyl)-4-pyrimidone (2.47 g, 0.100 mol) in ethanol (12 ml) was boiled under reflux for 22 hours and evaporated to dryness. The residue was washed with water to give 2-[2-(5-dimethylaminomethyl-2-furylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidone and this was treated with dilute ethanolic hydrogen chloride and dried. The residue was recrystallised from methanol/2-propanol and from methanol to give 2-[2-(5-dimethylaminomethyl-2-furylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidone trihydrochloride (2.61 g) m.p. 205°-208°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04234588
Source datasetuspto-grants-1980_11
ORD IDord-28bb05bbf032412a9dbc6aff102b204c
Source noteuspto-grants-1980_11