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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473660Generated: October 27, 2026

Water → 7-Bromo-4-(2-methoxy-4-(trifluoromethyl)phenyl)-2-methylquinazoline

https://huagongshe.com/reaction/1473660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Bromo-4-chloro-2-methylquinazolineHCID 22247819—
Reactant(2-Methoxy-4-(trifluoromethyl)phenyl)boronic acidHCID 24901776—
CatalystHCID 178418807HCID 178418807—
Solvent1,4-DioxaneHCID 31275—
Product7-Bromo-4-(2-methoxy-4-(trifluoromethyl)phenyl)-2-methylquinazolineHCID 8668773551.7%

Reaction Steps

A solution of PdCl2(dppf)-CH2Cl2 adduct (0.159 g, 0.194 mmol), (2-methoxy-4-(trifluoromethyl)phenyl)boronic acid (0.940 g, 4.27 mmol), 7-bromo-4-chloro-2-methylquinazoline (ACES Pharma, 1.000 g, 3.88 mmol), and potassium carbonate (2.147 g, 15.53 mmol) in 12 mL dioxane was treated with 4 mL water and was allowed to stir overnight at room temperature. LC/MS showed mostly product, so the aqueous layer was removed, and the reaction mixture was concentrated. Purification of the crude residue by silica gel column chromatography (0-50% EtOAc/heptane) gave 7-bromo-4-(2-methoxy-4-(trifluoromethyl)phenyl)-2-methylquinazoline (0.797 g, 2.007 mmol, 51.7% yield). (M+H)+=396.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-2cc2beaecb2a41c5b7644b8b2a313520
Source noteuspto-grants-2015_04