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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855686Generated: October 28, 2026

Sodium hydride → HCID 17942744, compound

https://huagongshe.com/reaction/855686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Phenyl-4H-pyrazol-3-olHCID 78577—
ReactantHCID 10681434HCID 10681434—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 17942744HCID 1794274446%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-Phenyl-4,5-dihydro-1H-pyrazol-5-one (270 mg, 1.68 mmol), (J. Org. Chem., 1967, 32, 3321-3324), was added in portions over 10 minutes to a suspension of sodium hydride (70 mg, 1.68 mmol, prewashed with pentane) in DMF (3 ml) under nitrogen. After stirring for 1 hour at ambient temperature 4-chloro-7-(2-methoxyethoxy)quinazoline (160 mg, 0.67 mmol) was added and the mixture was heated for 1 hour at 60° C. After cooling, the mixture was diluted with saturated aqueous ammonium chloride solution and partitioned between ethyl acetate and water. The organic layer was washed with water, brine, dried (MgSO4) and the volatiles removed by evaporation. The residue was purified by column chromatography eluting with methanol/methylene chloride (5/95). The volatiles were removed by evaporation, the residual solid was dissolved in methylene chloride and 3M ethereal hydrogen chloride (0.5 ml) was added. After removal of the solvent by evaporation, the residue was triturated with ether, collected by filtration and dried under vacuum to give 7-(2-methoxyethoxy)-4-(5-phenylpyrazol-3-yloxy)quinazoline hydrochloride (120 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262201B1
Source datasetuspto-grants-2007_08
ORD IDord-e7b3927441af45798ca0159fef8f533b
Source noteuspto-grants-2007_08