Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195435Generated: October 31, 2026

Triethylamine → HCID 53742305, compound

https://huagongshe.com/reaction/1195435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-FluorobenzylamineHCID 66649—
Reactant5-Amino-2,4-dichloropyrimidineHCID 257797—
Solvent1-ButanolHCID 263—
ProductHCID 53742305HCID 53742305—

Reaction Steps

A mixture of 0.5 g (3.1 mmol) of 5-amino-2,4-dichloropyrimidine [D. T. Hurst, Heterocycl. 22, 79 (1984)], 0.35 ml (3.1 mmol) of 2-fluorobenzylamine and 0.46 ml (3.4 mmol) of triethylamine in 8 ml of 1-butanol is heated under reflux for 24 hours. The reaction mixture is then cooled to 0°. The resulting beige-coloured suspension is filtered with suction and the filter cake is washed with cyclohexane and suspended in water for 30 minutes at room temperature with stirring. The suspension is again filtered with suction and the filter cake is dried under a high vacuum at 100° over tetraphosphorus decaoxide. In this manner 5-amino-2-chloro-4-[N-(2-fluorobenzyl)amino]-pyrimidine is obtained in the form of beige-coloured crystals having a melting range of from 224° to 225°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110818
Source datasetuspto-grants-1992_05
ORD IDord-da1181527b12482282af5f93fd4c4744
Source noteuspto-grants-1992_05