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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81500Generated: October 30, 2026

Water → 2-(4-Methoxy-3,5-dimethylphenyl)-5-methylsulfanyl-7-propoxyoxazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/81500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-BromopropaneHCID 7840—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178489873HCID 178489873—
SolventDimethylformamideHCID 6228—
Product2-(4-Methoxy-3,5-dimethylphenyl)-5-methylsulfanyl-7-propoxyoxazolo[5,4-d]pyrimidineHCID 6729417337.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

5.9 g of 2-(4-methoxy-3,5-dimethylphenyl)-5-methylsulfanyloxazolo[5,4-d]pyrimidin-7-ol were dissolved in 150 ml of N,N-dimethylformamide, and 7.7 g of potassium carbonate and then 2.7 g of 1-bromopropane were added. The solution was stirred at 60° C. for 5 h and then, after cooling, poured into 150 ml of water. The precipitate was filtered off with suction. The regioisomer mixture obtained was purified by silica gel chromatography (50 g silicon dioxide solute cartridge, heptane/ethyl acetate 9/1). In addition to 1.4 g of 2-(4-methoxy-3,5-dimethylphenyl)-5-methylsulfanyl-6-propyl-6H-oxazolo[5,4-d]pyrimidin-7-one (LC/MS (Method LC1): Rt=1.43 min; m/z=360.13 [M+H]+), 2.5 g of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846691B2
Source datasetuspto-grants-2014_09
ORD IDord-66c7ea0e04ad4981aaff8f7a3dd08b15
Source noteuspto-grants-2014_09