HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386148Generated: October 30, 2026
Potassium Carbonate → HCID 59526281, compound
https://huagongshe.com/reaction/386148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-6-methylpyridine | HCID 79205 | — |
| Reactant | 2-Aminothiophene-3-carboxamide | HCID 699495 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 59526281 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367706B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-f66be0e0302442d19a22292deca01a66 |
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| Source note | uspto-grants-2013_02 |
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