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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095471Generated: October 26, 2026

2-(4-Aminophenyl)ethylamine → N-(4-aminophenethyl)-5,6-diphenylfuro[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1095471

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Aminophenyl)ethylamineHCID 72895—
Reactant4-Chloro-5,6-diphenylfuro[2,3-d]pyrimidineHCID 11449637—
Solvent1-ButanolHCID 263—
ProductN-(4-aminophenethyl)-5,6-diphenylfuro[2,3-d]pyrimidin-4-amineHCID 4685504374%

Reaction Steps

4-Chloro-5,6-diphenylfuro[2,3-d]pyrimidine (0.200 g) and 4-(2-aminoethyl)aniline (0.107 g) in n-butanol (5 mL) were heated at 80° C. for 16 h. The reaction mixture was concentrated and the residue was partitioned between water and ethyl acetate. The organic layer was concentrated and the crude compound was purified by silica gel column chromatography using a mixture of dichloromethane:methanol (40:1), to give N-(4-aminophenethyl)-5,6-diphenylfuro[2,3-d]pyrimidin-4-amine (0.195 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138194B2
Source datasetuspto-grants-2012_03
ORD IDord-df27339b0eb54779996fe49ae54f0d63
Source noteuspto-grants-2012_03