HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197541Generated: October 26, 2026
Potassium Fluoride → (Z)-6-(2-ethoxyvinyl)-8-phenyl-[1,2,4]triazolo[4,3-a]pyridine
https://huagongshe.com/reaction/2197541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | cis-1-Ethoxy-2-(tri-n-butylstannyl)ethylene | HCID 5706773 | — |
| Reactant | 6-Bromo-8-phenyl-[1,2,4]triazolo[4,3-a]pyridine | HCID 58207919 | — |
| Catalyst | Tetraethylammonium Chloride | HCID 5946 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (Z)-6-(2-ethoxyvinyl)-8-phenyl-[1,2,4]triazolo[4,3-a]pyridine | HCID 58207976 | 52% |
Reaction Steps
A mixture of 6-bromo-8-phenyl-[1,2,4]triazolo[4,3-a]pyridine (26.1 mg, 0.095 mmol), (Z)-tributyl(2-ethoxyvinyl)stannane (34.6 mg, 0.095 mmol) and tetraethylammonium chloride (16 mg, 0.095 mmol) in DMF (0.5 mL) was added PdCl2(PPh3)2 (2 mg, 0.005 mmol). The reaction was heated at 80° C. overnight, cooled to rt, added an aqueous of KF (1.1 eq) in water (95 μL) and further stirred for 30 mins, then diluted with ethyl acetate (2 mL), filtered and rinsed with ethyl acetate (8 mL). The mixture was then washed with water (2×2 mL), separated, dried and concentrated. The residue was purified by a flash column using a gradient of ethyl acetate in hexane (50-75%) as an eluent to give compound (13 mg, 52% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338604B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-627e866f29a844be9ace32299abed9da |
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| Source note | uspto-grants-2012_12 |
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