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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166700Generated: October 31, 2026

5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamine → HCID 13137363, compound

https://huagongshe.com/reaction/2166700

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(((2-Aminoethyl)thio)methyl)-N,N-dimethyl-2-furanmethanamineHCID 162203—
ReactantHCID 13137346HCID 13137346—
SolventPyridineHCID 1049—
ProductHCID 13137363HCID 13137363—

Reaction Steps

A solution of 2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamine (1.29 g) and 2-nitroamino-5-(5-dimethylaminomethyl-2-furanylmethyl)-4-pyrimidone in pyridine (15 ml) was heated under reflux for about 20 hr. The pyridine was evaporated at reduced pressure. The last traces of pyridine were removed by azeotroping with water and water removed by azeotroping with n-propanol. The oily residue was chromatographed on a silica gel column eluting with methanol in ethyl acetate (10% v/v). Evaporation of the eluant yielded 2-[2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamino]-5-(5-dimethylaminomethyl-2-furanylmethyl)-4-pyrimidone as an oil which was converted to its trihydrochloride using an excess of ethanolic HCl. The salt was recrystallised from isopropanol yielding a white solid (0.72 g) m.p. 181°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04388317
Source datasetuspto-grants-1983_06
ORD IDord-8329ebea82264fdfbd8e69120e63b925
Source noteuspto-grants-1983_06