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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786924Generated: October 30, 2026

N-methyl-2-pyrrolidone → N-[4-(benzyloxy)-3-methoxyphenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amine

https://huagongshe.com/reaction/1786924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-(Benzyloxy)-3-methoxyanilineHCID 27226—
Reactant4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
SolventMethanolHCID 887—
ProductN-[4-(benzyloxy)-3-methoxyphenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amineHCID 5759732859.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (200 mg), 4-(benzyloxy)-3-methoxyaniline (298 mg) and 1-methyl-2-pyrrolidone (5 mL) was stirred at 80° C. for 4 hrs. Methanol and activated carbon were added to the reaction mixture and the mixture was stirred. The activated carbon was filtered off, aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent, methanol:ethyl acetate=10:80→20:80) and recrystallized from methanol-ethyl acetate to give the title compound (269 mg) as a pale-gray powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-bc3f968d5e284d2d81428d6a5969d4f0
Source noteuspto-grants-2009_03