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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925983Generated: October 28, 2026

Methyl iodide → 4-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1925983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidineHCID 5942450593.1%

Reaction Steps

To a suspension of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (320 mg) in N,N-dimethylformamide (2.0 mL), was added potassium carbonate (452 mg) under ice-cooling, and the mixture was stirred while warming to room temperature for 15 min. Iodomethane (444 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 (25 mL) and extracted with ethyl acetate (30 mL×3). The organic layer was 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 (325 mg) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-faa9c224fa7b4f379b16967ef7d7af07
Source noteuspto-grants-2012_05