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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677713Generated: October 30, 2026

Ethanol → HCID 58138783, compound

https://huagongshe.com/reaction/1677713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant6-Bromo-1-(4-fluoro-phenyl)-1H-indazole-4-carboxylic acid 4-methylsulfamoyl-benzylamideHCID 44469803—
ReactantHCID 178418416HCID 178418416—
CatalystBis(benzonitrile)palladium chlorideHCID 498840—
Catalyst1,1`-Bis(diphenylphosphino)ferroceneHCID 15241612—
SolventWaterHCID 962—
ProductHCID 58138783HCID 58138783—

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008327B2
Source datasetuspto-grants-2011_08
ORD IDord-93d06e257ba24088b6cf5693cdead96c
Source noteuspto-grants-2011_08