Dichloromethane → 5-(4-(4-(3-Fluorobenzyloxy)-3-bromophenylamino)quinazolin-6-yl)furan-2-carbaldehyde

Participants

Reaction Conditions

Reaction Steps

Under nitrogen atmosphere, Pd(dppf)2Cl2 (80 mg) was added to a mixture of N-(4-(3-fluorobenzyloxy)-3-bromophenyl)-6-iodoquinazolin-4-amine (550 mg, 1 mmole), 5-formylfuran-2-yl-2-boronic acid (170 mg, 1.2 mmole) and 2M K2CO3 (4 mL) in Ethanol (4 mL) and DME (4 mL). The reaction mixture was heated at 75° C. for 4 h and cooled down to room temperature. Methylene chloride (30 mL) was added and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography, eluting with 20% methanol in dichloromethane to give the desired product as white solid (460 mg). LCMS ESI(+) m/z: 519 (M+1). Yield: 89%.

Provenance & Evidence