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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9894Generated: October 29, 2026

Ethylenediamine → 2-(2-Amino-ethyl-amino)-6-(3-chloro-phenylamino)-9-ethyl-9H-purine

https://huagongshe.com/reaction/9894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
Reactant2-Chloro-n-(3-chlorophenyl)-9-ethyl-9h-purin-6-amineHCID 11001320—
SolventEthyl AcetateHCID 8857—
Product2-(2-Amino-ethyl-amino)-6-(3-chloro-phenylamino)-9-ethyl-9H-purineHCID 9949448—

Reaction Conditions

Temperature150 °C

Reaction Steps

250 mg (0.81 mmol) of 2-chloro-6-(3-chloro-phenyl-amino)-9-ethyl-9H-purine are dissolved in 5.8 ml (97 mmol) of ethylenediamine and the solution is heated under reflux for 3 hours (oil bath temperature of 150° C.). After cooling to room temperature, the reaction mixture is taken up in ethyl acetate (250 ml) and extracted with water (150 ml). The aqueous phase is extracted twice with ethyl acetate and the combined organic extracts are washed successively with saturated sodium bicarbonate solution, water and saturated sodium chloride solution and dried over magnesium sulfate. After filtration, the filtrate is concentrated under reduced pressure at 35° C. and the residue is dried under an HV. The crude product is recrystallized from diethyl ether. 2-(2-Amino-ethyl-amino)-6-(3-chloro-phenylamino)-9-ethyl-9H-purine is obtained; Rf=0.22 (methylene chloride:methanol:concentrated aqueous ammonium hydroxide solution=900:100:1); FAB-MS: (M+H)+=322; m.p. 79–80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091346B1
Source datasetuspto-grants-2006_08
ORD IDord-0e289eb070e44fd5bd336895d77677ad
Source noteuspto-grants-2006_08