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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926115Generated: November 1, 2026

Water → 6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1926115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-Phenoxy-6-prop-1-yn-1-ylpyrimidin-5-amineHCID 56851054—
SolventTetrahydrofuranHCID 8028—
Product6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidineHCID 5685105574.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Phenoxy-6-prop-1-yn-1-ylpyrimidin-5-amine (776.0 mg) was dissolved in tetrahydrofuran (30 mL) and cooled to 0° C. To this solution was added dropwise a 1.0 M solution (4 mL) of potassium tert-butoxide in tetrahydrofuran, and the mixture was stirred at room temperature for 30 min. 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=67:33→20:80) to give the title compound (578.6 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-9ef2866dab4842379359b9a7c29f4472
Source noteuspto-grants-2012_05