9-Oxofluorene-4-carboxylic acid → HCID 67358877, compound

Participants

Reaction Conditions

Reaction Steps

The procedure used in Example 68 is followed. In a 100 ml round-bottomed flask under an argon atmosphere, heat, at 115° C. for 6 hours, a suspension of 1.7 g of (6-amino-2,3-difluorophenyl)amide of 9-oxo-9H-fluorene-4-carboxylic acid, obtained in the previous stage, in 35 ml of acetic acid. After cooling, bring to dryness under reduced pressure. Take the residue up in water and bring to pH=8 by adding a 10% saturated aqueous solution of sodium hydrogen carbonate, with water. The precipitate that formed is filtered off, washed with water, and rinsed with diisopropyl ether. In this way, we obtain 1.5 g of 4-(4,5-difluoro-1H-benzimidazol-2-yl)-9H-fluoren-9-one, in the form of an orange powder, which is used as it is in the following stage, with the following characteristics:

Provenance & Evidence