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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967159Generated: October 31, 2026

Potassium Carbonate → HCID 44610524, compound

https://huagongshe.com/reaction/1967159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIodobenzeneHCID 11575—
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—
ProductHCID 44610524HCID 44610524—

Reaction Conditions

Temperature100 °C

Reaction Steps

A sealed tube was charged with a stir bar and 2-amino-5-[2,6-difluoro-4-(1-hydroxy-1-methylethyl)phenyl]thiophene-3-carboxamide (150 mg, 0.480 mmol) and iodobenzene (98 mg, 0.480 mmol), Pd2(dba)3 (44 mg, 0.048 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (114 mg, 0.240 mmol), and potassium carbonate (73 mg, 0.528 mmol). The tube was evacuated and backfilled with argon three times. Fully degassed tert-amyl alcohol (1.6 mL) was added to the mixture via syringe. The solution was sealed and stirred overnight in an oil bath at 100° C. The following day, the reaction was allowed to cool to room temperature, taken up in ethyl acetate, and washed with aqueous sodium bicarbonate and brine. The organic layers were collected, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Purification was conducted via silica gel chromatography (0-3% methanol in ethyl acetate). Fractions containing product were concentrated under reduced pressure, taken up in ethyl acetate and methanol, and recrystallized out using hexanes to yield the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420695B2
Source datasetuspto-grants-2013_04
ORD IDord-f03fec0f40f141369261ae6a7113a1a0
Source noteuspto-grants-2013_04