Potassium Carbonate → N-(4-fluorophenyl)-7-methoxy-6-(3-(tetrahydro-2H-[1,4]dioxino[2,3-c]pyrrol-6(3H)-yl) propoxy) quinazolin-4-amine

Participants

Reaction Conditions

Reaction Steps

A mixture of hexahydro-2H-[1,4]dioxino[2,3-c]pyrrole (0.39 g, 3.0 mmol, 1.0 eq), N-(4-fluorophenyl)-6-(3-chloropropoxy)-7-methoxyquinazolin-4-amine (868 mg, 2.40 mmol, 0.80 eq), anhydrous K2CO3 (2.07 g, 15.0 mmol, 5.0 eq) and tetrabutylammonium iodide (55 mg, 0.15 mmol, 0.05 eq) in DMF (10 mL) was heated at 70° C. for 11 h. The reaction mixture was cooled to room temperature and quenched with water (10 mL). The resulted mixture was diluted with EtOAc (20 mL) and the organic phase was separated from the mixture. The water phase was extracted with EtOAc (20 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (20:1 (v/v) CH2Cl2/CH3OH) to give the crude product, which was recrystallized from CH2Cl2/PE to afford the title compound as a pale yellow solid (196 mg, 22.00%), HPLC:96.21%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 455.2 (M+1); 1H NMR (400 MHz, CDCl3) δ: 2.00 (2H, m), 2.63 (2H, m), 2.72 (2H, m), 2.90 (2H, dd, J=2.8, 6.1 Hz), 3.28 (1H, br s), 3.52 (2H, m), 3.76 (2H, m), 3.91 (3H, s), 4.05 (4H, d, J=4.4 Hz), 7.03 (1H, t, J=8.4 Hz), 7.18 (1H, s), 7.29 (1H, s), 7.63 (1H, dd, J=4.8, 8.4 Hz), 8.42 (1H, br s), 8.60 (1H, s) ppm.

Provenance & Evidence