Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Bromo-1-(4-fluoro-phenyl)-1H-indazole-4-carboxylic acid 4-methylsulfamoyl-benzylamide | HCID 44469803 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Bis(benzonitrile)palladium chloride | HCID 498840 | — |
| Catalyst | 1,1`-Bis(diphenylphosphino)ferrocene | HCID 15241612 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58138783 | HCID 58138783 | — |
Reaction Steps
A mixture of 6-bromo-1-(4-fluoro-phenyl)-1H-indazole-4-carboxylic acid 4-methylsulfamoyl-benzylamide (0.2 g, 0.4 mmol), triethylamine (0.1 g, 0.9 mmol), dichlorobis(benzonitrile)palladium (0.02 g, 0.05 mmol) and 1,1-bis(diphenylphosphino)ferrocene (0.03 g, 0.05 mmol) was charged in a sealed tube with absolute ethanol (15 mL). The solution was placed under 15 bars of carbon monoxide and warmed at 140° C. for 4 hours. The mixture was cooled to room temperature and returned to atmospheric pressure. The reaction was diluted with water (30 mL) and the solid was collected by filtration. The filtrate was diluted with water (20 mL) and ethyl acetate (20 mL). The organic layer was separated and washed with brine (10 mL) and dried over sodium sulfate and concentrated. The residue was purified by silica gel chromatography eluting with a gradient of 30-70% ethyl acetate in hexanes to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008327B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-93d06e257ba24088b6cf5693cdead96c |
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| Source note | uspto-grants-2011_08 |
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