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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408474Generated: October 29, 2026

Chloride → 2-(2,6-Difluorophenyl)-8-methoxyquinazoline

https://huagongshe.com/reaction/408474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Difluorophenylboronic acidHCID 2734336—
Reactant2-Chloro-8-methoxyquinazolineHCID 19988695—
CatalystHCID 178418807HCID 178418807—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product2-(2,6-Difluorophenyl)-8-methoxyquinazolineHCID 58386803—

Reaction Conditions

Temperature130 °C

Reaction Steps

2-chloro-8-methoxyquinazoline (1.0 eq), 2,6-difluorophenylboronic acid (1.5 eq), and DIPEA (3 eq) was mixed with toluene and ethanol (1:1, 0.5M) in a microwave vial. The reaction mixture was degassed by anhydrous N2 stream for 5 min followed by the addition of Pd(dppf)Cl2-DCM (0.1 eq). The reaction mixture was stirred at 130° C. for 30 min in microwave. Solvents were removed under reduced pressure. The crude product was purified by column (ethyl acetate:hexanes=1:1) to give the mixture of starting material chloride and desired product. The mixture was treated with 1N HCl in 1,4-dioxane. Solvents were removed under reduced pressure. The residue was dissolved in ethyl acetate (150 mL), and washed with NaHCO3, brine, then dried over MgSO4, filtered, and evaporated under reduced pressure to give crude product, which was purified by column (ethyl acetate:hexanes=1:1) to yield 2-(2,6-difluorophenyl)-8-methoxyquinazoline (46%). LC/MS (m/z): 273.0 (MH+), Rt=0.78.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759338B2
Source datasetuspto-grants-2014_06
ORD IDord-52d06594b5f44f619c4684a1d851b1ed
Source noteuspto-grants-2014_06