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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786887Generated: October 29, 2026

Iodoethane → 4-Chloro-5-ethyl-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1786887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Chloro-5-ethyl-5H-pyrrolo[3,2-d]pyrimidineHCID 7141346079.1%

Reaction Steps

To a suspension of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (200 mg) in N,N-dimethylformamide (1.3 mL) was added potassium carbonate (269 mg) under ice-cooling, and the mixture was stirred while warming to room temperature for 15 min. Iodoethane (305 mg) was added to the reaction mixture, and the mixture was stirred at room temperature for 3 hrs. The reaction mixture was diluted with water (20 mL) and extracted with ethyl acetate (30 mL×3). The organic layer washed with saturated brine (20 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=80/20→10/90). The object fraction was concentrated under reduced pressure and dried to give the title compound (187 mg) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-5d84124ecc41478eb68773bd82261c72
Source noteuspto-grants-2009_03