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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387782Generated: October 30, 2026

4-Nitrophenol → 4-(4-nitrophenoxy)-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/387782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant4-chloro-6-phenyl-7H-pyrrolo[2,3-d]pyrimidineHCID 22484442—
SolventWaterHCID 962—
Product4-(4-nitrophenoxy)-6-phenyl-7H-pyrrolo[2,3-d]pyrimidineHCID 5893131568.5%

Reaction Conditions

Temperature132.5 °C

Reaction Steps

After adding 123 mg of 4-nitrophenol, 136 mg of potassium carbonate and 1.5 ml of dimethylformamide to 113 mg of the 4-chloro-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine described in WO97/02266 and PCT/EP96/02728, and stirring the mixture for 15 hours at 130-135° C., and additional 60 mg of 4-nitrophenol and 75 mg of potassium carbonate were added and the mixture was stirred for 6 hours. After returning the mixture to room temperature, water was added, liquid separation and extraction were performed with an ethyl acetate-tetrahydrofuran mixed solvent, and the solid obtained by concentration to dryness was washed with ether to obtain 112 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-6729061283bb4f628e1b8e7c4eeb614b
Source noteuspto-grants-2013_02