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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890219Generated: October 29, 2026

Water → HCID 22249707, compound

https://huagongshe.com/reaction/890219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
Reactant2-MethoxyethylamineHCID 8018—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22249904HCID 22249904—
SolventDimethylformamideHCID 6228—
ProductHCID 22249707HCID 22249707—

Reaction Conditions

Temperature150 °C

Reaction Steps

7-Chloro-6-(3-chlorohexyl)-3-mesityl-2,5-dimethylpyrazolo[1,5-a]pyrimidine (170 mg, 0.406 mmol) was dissolved in 2-methoxyethylamine (2 mL), followed by heating under reflux for one hour. Water was added to the reaction mixture, followed by extracting with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate and evaporated, to give a pale yellow oil. The oil was dissolved in N,N-dimethylformamide (10 mL), and sodium iodide (62 mg, 0.416 mmol) and potassium carbonate (172 mg, 1.25 mmol) were added thereto. The mixture was stirred at 150° C. for two days. After cooling, water was added to the reaction mixture and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and then evaporated. The residue was purified by silica gel column chromatography (5-10% ethyl acetate/hexane), to give the title compound (60 mg, 0.143 mmol) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995163B2
Source datasetuspto-grants-2006_02
ORD IDord-dada9982e76341b68e1a63b1842f7920
Source noteuspto-grants-2006_02