HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 405785Erstellt: 24. Oktober 2026
3-Butenenitrile → Ethyl 6-(3-cyanoprop-1-enyl)imidazo[1,2-a]pyridine-3-carboxylate
https://huagongshe.com/de/reaction/405785
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3-Butenenitrile | HCID 8009 | — |
| Edukt | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Edukt | Bis(cyclohexylmethyl)amine | HCID 4594378 | — |
| Edukt | Ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate | HCID 22031055 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | Ethyl 6-(3-cyanoprop-1-enyl)imidazo[1,2-a]pyridine-3-carboxylate | HCID 78048051 | — |
Reaktionsschritte
A stirring mixture of ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s) (500 mg, 1.86 mmol), allyl cyanide (224 uL, 2.79 mmol), tris(dibenzylideneacetone)dipalladium(0) (26 mg, 0.028 mmol), [(t-Bu)3PH]BF4 (16 mg, 0.056 mmol), and N,N-dicyclohexylmethylamine (433 μL, 2.04 mmol) in anhydrous 1,4-dioxane (6 mL) was heated at 95° C. overnight. The reaction was cooled to room temperature and filtered. The solvent was concentrated. The crude product was purified by silica chromatography to give ethyl 6-(3-cyanoprop-1-enyl)imidazo[1,2-a]pyridine-3-carboxylate (24v). MS m/z 256.4 (M+1)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754071B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-e61c8da854ca45f3861f1032aeac4086 |
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| Quellennotiz | uspto-grants-2014_06 |
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