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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967151Generated: October 26, 2026

Potassium Carbonate → 5-[2,6-Difluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-{[4-(methylsulfonyl)phenyl]amino}thiophene-3-carboxamide

https://huagongshe.com/reaction/1967151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-(methylsulphonyl)benzeneHCID 77014—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant2-Amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamideHCID 59525619—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthanolHCID 702—
Product5-[2,6-Difluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-{[4-(methylsulfonyl)phenyl]amino}thiophene-3-carboxamideHCID 44610063—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (0.1 g, 0.320 mmol), 4-bromophenyl methyl sulfone (0.075 g, 0.320 mmol), Pd2 dba3 (0.029 g, 0.032 mmol), K2CO3 (0.049 g, 0.352 mmol) and X-Phos (0.076 g, 0.160 mmol) were added to a 5 mL microwave vial. Degassed EtOH (1 mL) was added and the vial evacuated and back-filled with N2 (×3). The resulting mixture was stirred at 100° C. overnight. Room temperature was attained, MeOH was added and the solvent removed in vacuo while loading onto silica. Purification of the residue by MPLC (0-10% MeOH—CHCl3) gave 5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]-2-{[4-(methylsulfonyl)phenyl]amino}thiophene-3-carboxamide as a beige solid after triturating in DCM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420695B2
Source datasetuspto-grants-2013_04
ORD IDord-3990bd39f71a43ddafd560707804bd84
Source noteuspto-grants-2013_04