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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294040Generated: October 25, 2026

1-(3-Chlorophenyl)piperazine → 5-[4-(3-Chloro-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/2294040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chlorophenyl)piperazineHCID 1355—
ReactantTriethylamineHCID 8471—
Reactant5-(Bromomethyl)pyrimidine-2,4-diamine dihydrobromideHCID 21473608—
SolventTetrahydrofuranHCID 8028—
Product5-[4-(3-Chloro-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamineHCID 2147367363%

Reaction Steps

A solution of 13.5 g (0.050 mol) of 1-(3-chloro-phenyl)-piperazine in 500 ml of tetrahydrofuran was treated with 35 ml (0.25 mol) of triethylamine and 18.2 g (0.050 mol) of 5-bromomethyl-pyrimidine-2,4-diamine dihydrobromide and the mixture was stirred at room temperature under argon for 16 hours. The suspension obtained was suction filtered and the filtrate was completely freed from the solvents. The residue was chromatographed over silica gel with acetonitrile/methanol 1:1 as the eluent and digested in diethyl ether. 10 g (63%) of 5-[4-(3-chloro-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamine were obtained as beige crystals; m.p. 222°-226°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688798
Source datasetuspto-grants-1997_11
ORD IDord-82a69ec5510545d78b21805f22dd62c6
Source noteuspto-grants-1997_11