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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9898Generated: October 26, 2026

Isopropyl iodide → 2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amine

https://huagongshe.com/reaction/9898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantCesium carbonateHCID 10796—
Reactant2-chloro-N-(3-chlorophenyl)-9H-purin-6-amineHCID 21988232—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product2-Chloro-N-(3-chlorophenyl)-9-isopropyl-9H-purin-6-amineHCID 21988248—

Reaction Steps

500 mg (1.78 mmol) of 2-chloro-6-(3-chloro-phenyl-amino)-purine are dissolved in a mixture of 29.5 ml of DMF/water (85/15) and 5 ml of dioxane by means of gentle heating. 870 mg (2.67 mmol) of caesium carbonate, followed by 1.78 ml (17.8 mmol) of isopropyl iodide are added at room temperature. The reaction mixture is stirred at room temperature for 18 hours. To bring the reaction to completion, the reaction mixture is stirred at 45° C. for a further 24 hours. When the reaction has ended, the reaction mixture is diluted with ethyl acetate, washed with water (2 times) 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 resulting crude product is purified by crystallization from diethyl ether/hexane. 2-Chloro-6-(3-chloro-phenyl-amino)-9-isopropyl-9H-purine is obtained; Rf=0.46 (ethyl acetate); m.p. 128–129° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091346B1
Source datasetuspto-grants-2006_08
ORD IDord-74fde67f2a9f47cb945db7fa6bea0160
Source noteuspto-grants-2006_08