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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926116Generated: November 2, 2026

Water → 2-[2-(6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy]ethyl benzoate

https://huagongshe.com/reaction/1926116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidineHCID 56851055—
Reactant2-{2-[(Methylsulfonyl)oxy]ethoxy}ethyl benzoateHCID 86615775—
SolventDimethylformamideHCID 6228—
Product2-[2-(6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy]ethyl benzoateHCID 5685105693.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

6-Methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine (299.9 mg) and 2-{2-[(methylsulfonyl)oxy]ethoxy}ethyl benzoate (464.1 mg) were dissolved in N,N-dimethylformamide (7 mL), potassium carbonate (431 mg) was added, and the mixture was stirred at 60° C. for 21 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified by silica gel column chromatography (eluent, hexane:ethyl acetate=80:20→20:80) to give the title compound (517.8 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-722967ff98684ac6bab65646ac8eb962
Source noteuspto-grants-2012_05