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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386148Generated: October 30, 2026

Potassium Carbonate → HCID 59526281, compound

https://huagongshe.com/reaction/386148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-6-methylpyridineHCID 79205—
Reactant2-Aminothiophene-3-carboxamideHCID 699495—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Solvent2-Methyl-2-butanolHCID 6405—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59526281HCID 59526281—

Reaction Steps

A suspension of 2-aminothiophene-3-carboxamide (6.26 g, 44.0 mmol), potassium carbonate (6.08 g, 44.0 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1-biphenyl (0.667 g, 1.40 mmol), dibenyzlideneacetone bis(triphenylphosphine) (0.293 g, 0.32 mmol), and 2-bromo-6-methylpyridine (4.55 mL, 40 mmol) in tert-amyl alcohol (80 mL) in a 250 mL round bottom flask with attached reflux condenser was placed under an argon atmosphere by performing six vacuum/argon flush cycles. The reaction was heated to reflux for 18 hours. The flask was charged with more 2-dicylohexylphosphino-2′,4′,6′-triisopropyl-1,1-biphenyl (0.330 g, 0.7 mmol) and dibenyzlideneacetone bis(triphenylphosphine) (0.146 g, 0.160 mmol) and refluxed for an additional 24 hours. The reaction mixture was diluted with ethyl acetate (200 mL) and saturated aqueous sodium bicarbonate, and this suspension was filtered. The layers of the filtrate were separated and the organic layer was washed with brine (100 mL), dried over sodium sulfate, filtered, and concentrated. The resulting solid was triturated with a 1:1 mixture of ethyl acetate and hexanes to afford the title compound as a grey solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-f66be0e0302442d19a22292deca01a66
Source noteuspto-grants-2013_02