Ammonia → HCID 66775458, compound

Participants

Reaction Conditions

Reaction Steps

A 250 ml round-bottomed flask equipped with a magnetic stirrer and with a septum having a top-mounted argon intake is charged with 2.6 g of 2,6-difluoro-N-[5′(4-fluorophenyl)-1H-pyrazol-4-yl]benzamide, 60 ml of phenylphosphine dichloride and 17.5 g of phosphorus pentoxide. After 23 h of heating at 165° C., the mixture is cooled to RT and then poured into a mixture of 260 ml of water and 400 g of ice. The temperature rises to 40° C. The mixture is neutralized by slow addition of 120 ml of 28% aqueous ammonia. It is extracted with AcOEt, washed with saturated NaCl solution and dried over MgSO4, then concentrated under RP. The product is purified by flash chromatography on silica gel (15-40 μm), eluting with a mixture of DCM and methanol (99/1 by vol.), to give 680 mg of 5-(2,6-difluorophenyl)-7-fluoro-1H-pyrazolo[4,3-c]isoquinoline (cream solid). MS (E/I): m/z=299 (M+); 1H NMR: 7.34 (t, J=7.8 Hz, 2 H) 7.38 (broad m, 1 H) 7.70 (m, 1 H) 7.96 (broad t, J=9.1 Hz, 1 H) 8.48 (broad s, 1 H) 8.63 (dd, J=9.1, 5.6 Hz, 1 H) 14.29 (broad s, 1 H).

Provenance & Evidence