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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208121Generated: November 1, 2026

Bromine → 7-Bromo-4-chloro-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/2208121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant4-chloro-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidineHCID 18511061—
SolventDichloromethaneHCID 6344—
Product7-Bromo-4-chloro-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidineHCID 86666637—

Reaction Conditions

Temperature10 °C

Reaction Steps

4-Chloro-2,6-dimethyl-5H-pyrrolo[3,2-d]pyrimidine from example A7 (10.90 g; 60.00 mmol) is dissolved in dichloromethane (120 mL). The stirred mixture is cooled to 10° C. Br2 (3.08 mL; 60.00 mmol) dissolved in dichloromethane (20 mL) is added dropwise within 25 minutes. The resulting precipitate is collected by suction filtration, suspended in Na2SO3 (5% solution) (100 mL) and is stirred for 30 minutes at ambient temperature. After filtratrion the product is dissolved in acetonitrile (1000 mL), refluxed for one hour and filtered while still hot. The solvent is removed under reduced pressure until the product starts to precipitate. Precipitation of the product is completed by addition of cyclohexane and cooling to 0° C. for several hours. The solid is collected by suction filtration, washed with cyclohexane and dried in vacuum at 50° C. over night to yield the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376442B2
Source datasetuspto-grants-2016_06
ORD IDord-f0de2a2be8dd4b1690734f206b911e03
Source noteuspto-grants-2016_06