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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520382Generated: November 4, 2026

Hydrochloric Acid → HCID 67298513, compound

https://huagongshe.com/reaction/1520382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
ReactantHCID 71274524HCID 71274524—
CatalystHCID 178418807HCID 178418807—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67298513HCID 6729851330%

Reaction Conditions

Temperature90 °C

Reaction Steps

6-Bromo-N,5-dimethyl-2-(pyridin-3-yl)quinazolin-4-amine (350 mg, 1.06 mmol), 2,4-difluorophenylboronic acid (252 mg, 1.595 mmol), K3PO4 (677 mg, 3.19 mmol) and Pd(dppf)Cl2—CH2Cl2 (87 mg, 0.106 mmol) were dissolved in the mixed solvent of 1,4-dioxane (10 mL) and water (1 mL). The resulting mixture was stirred at 90° C. for 2.5 hours under N2. After the reaction was completed, water was added to the mixture and extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over Na2SO4. After filtration and evaporation, the crude product was purified by column chromatography on NH-silica gel (eluted with isocratic 33% ethyl acetate/67% hexane) to give a white powder. The solid was suspended in ethanol and 5N HCl (1.0 mL) was added to the mixture. The mixture was sonicated for 10 min and the resultant precipitate was collected by filtration and dried to give 139 mg of 6-(2,4-difluorophenyl)-N,5-dimethyl-2-(pyridin-3-yl)quinazolin-4-amine dihydrochloride as a pale yellow powder in a 30% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073890B2
Source datasetuspto-grants-2015_07
ORD IDord-4ca9318612764db9b4521fc9cf991324
Source noteuspto-grants-2015_07