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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925975Generated: October 31, 2026

4-chloro-5H-pyrrolo[3,2-d]pyrimidine → HCID 57597349, compound

https://huagongshe.com/reaction/1925975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
ReactantHCID 63423601HCID 63423601—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventSodium BicarbonateHCID 516892—
ProductHCID 57597349HCID 5759734984.6%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (61 mg) in 1-methyl-2-pyrrolidone (0.8 mL), was added ethyl 5-amino-2-(3,5-dichlorophenoxy)benzoate (186 mg), and the mixture was heated to 140° C. and stirred for 2.5 hrs. The reaction mixture was allowed to cool to room temperature, diluted with 5% aqueous sodium hydrogen carbonate solution (20 mL), and extracted with a mixed solvent (25 mL×3) of ethyl acetate/tetrahydrofuran (1/1). The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (basic silica gel, eluent:hexane/ethyl acetate=8/2→0/10). The object fraction was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the resultant precipitate was collected by filtration and dried under reduced pressure to give the title compound (149 mg) as pale-yellow powder crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-c2f74d70edec46caa9c4d6776658b0bd
Source noteuspto-grants-2012_05