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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491671Generated: October 26, 2026

Potassium Carbonate → 4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-nitroaniline

https://huagongshe.com/reaction/491671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
Reactant4-Amino-3-NitrophenolHCID 3758882—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-nitroanilineHCID 17755401—

Reaction Steps

A solution of 4-amino-3-nitrophenol (0.8 g, 5.34 mmol, 1.2 eq) in DMSO (3.8 mL, 5×) was treated with KOt-Bu (0.6 g, 5.34 mmol, 1.2 eq), and the mixture was stirred at RT for 2 h. The contents were treated with 4-chloro-6,7-dimethoxyquinazoline (1.0 g, 4.45 mmol, 1.0 eq) and K2CO3 (0.33 g, 2.4 mmol, 0.53 eq) then heated at 110° C. for 16 h. The mixture was cooled to RT, diluted with EtOAc and washed with NaHCO3 (sat). To remove the emulsion, the mixture was filtered through Celite, then the organic layer was washed with brine, 1N NaOH, then brine again. The organic portion was dried with Na2SO4, filtered and evaporated to give the title compound as a brown solid. MS(MH+)=343.1; Calc'd 342.31 for C16H14N4O5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531553B2
Source datasetuspto-grants-2009_05
ORD IDord-4424411067454d5a8c4cc27aa1073154
Source noteuspto-grants-2009_05