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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984217Generated: November 3, 2026

Bromocyclopentane → HCID 11774121, compound

https://huagongshe.com/reaction/1984217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
Reactant[2-(3-Chloro-propoxy)-phenyl]-(2-chloro-9H-purin-6-yl)-amineHCID 178478467—
SolventDimethylformamideHCID 6228—
ProductHCID 11774121HCID 11774121—

Reaction Conditions

Temperature50 °C

Reaction Steps

[2-(3-Chloro-propoxy)-phenyl]-(2-chloro-9H-purin-6-yl)-amine (3 mmol), bromo-cyclopentane (4.1 mmol) and potassium carbonate (water free, 3.6 mmol) are suspended in DMF (20 ml) and heated up to 50° C. and the mixture is stirred at this temperature for 5 hours. After cooling to RT the mixture is poured on water and extracted 3 times with ethyl acetate. The combined organic phases are washed twice with brine and the extract is dried over sodium sulfate and evaporated. The residue is purified by flash chromatography on silica gel with (CH2Cl2/MeOH=20:1) as mobile phase. The product containing fractions are combined and evaporated. The product is cristallized from diethyl ether/pentane, filtered off and dried. A solid powder with mp. 110-112° C., Rf=0.78 (CH2Cl2/MeOH=20:1) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544688B2
Source datasetuspto-grants-2009_06
ORD IDord-b6b4b4d18b2243f9a57774e1472352fa
Source noteuspto-grants-2009_06