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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925981Generated: October 26, 2026

Cesium carbonate → 4-chloro-5-(2-ethoxyethyl)-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1925981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Bromoethyl ethyl etherHCID 61141—
Reactant4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-chloro-5-(2-ethoxyethyl)-5H-pyrrolo[3,2-d]pyrimidineHCID 8608482294.9%

Reaction Steps

To a suspension of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (500 mg) in N,N-dimethylformamide (4.5 mL) was added cesium carbonate (1324 mg) under ice-cooling, and the mixture was stirred while warming to room temperature for 15 min. 1-Bromo-2-ethoxyethane (1016 mg) was added to the reaction mixture, and the mixture was stirred at room temperature for 14 hrs. The reaction mixture was diluted with water (100 mL) and extracted with ethyl acetate (120 mL×3). The organic layer was washed with saturated brine (100 mL×3) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (silica gel, eluent:hexane/ethyl acetate=85/15→20/80). The object fraction was concentrated under reduced pressure and dried to give the title compound (697 mg) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-04d64085d53949ac886d7c0904f5fcf4
Source noteuspto-grants-2012_05