3-(Trifluoromethyl)pyrazole → 4,8-dichloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinoline

Participants

Reaction Conditions

Reaction Steps

A mixture of compound 220d (5 g, 19 mmol) and 3-trifluoromethyl)pyrazole 233a (7.76 g, 57 mmol) was heated at 120° C. for 4-6 hrs and the reaction was followed by LCMS and TLC. The reaction mixture was purified by silica gel column (mono and dipyrazole were separated) using DCM and heptane as mobile phase to yield compound 235a (3.5 g) in 51% yield.

Provenance & Evidence