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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547190Generated: October 26, 2026

Potassium Carbonate → Quinazoline

https://huagongshe.com/reaction/547190

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 numberUSRE042353E1
Source datasetuspto-grants-2011_05
ORD IDord-bf61367ae00d4dc4bc0f0807389af753
Source noteuspto-grants-2011_05