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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227938Generated: November 1, 2026

Potassium Carbonate → Quinazoline

https://huagongshe.com/reaction/2227938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
Reactant4-(Chloro-2-fluoroanilino)7-hydroxy-6-methoxyquinazolineHCID 135990682—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductQuinazolineHCID 9210172.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-(chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (3.28 g, 10 mmol), (prepared as described for the starting material in Example 2), 1-bromo-3-tetrahydropyranyloxypropane (2.5 g, 11 mmol) and potassium carbonate (5.0 g, 36 mmol) in DMF (50 ml) was stirred and heated at 90° C. for 3 hours. The reaction mixture was allowed to cool, was diluted with water (500 ml) and extracted with ethyl acetate (3×100 ml). The extracts were combined, washed with water (×3), and then brine, and dried (MgSO4). The solvent was removed by evaporation and the residue was purified by column chromatography eluting with ethyl acetate. The purified product was recrystallized from ethyl acetatethexane to give 4-(chloro-2-fluoroanilino)-6-methoxy-7-tetrshydropyran-2-yloxypropoxy)quinazoline (2.25 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414148B1
Source datasetuspto-grants-2002_07
ORD IDord-143c157314104ab2a8deaffbcf0976b8
Source noteuspto-grants-2002_07