HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 655809Erstellt: 25. Oktober 2026
Benzene, 2-iodo-1,3-dimethyl- → (E)-9-(2,6-dimethylstyryl)-2-chloro-N-(4-(dimethylphosphoryl)phenyl)-9H-purin-6-amine
https://huagongshe.com/reaction/655809
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzene, 2-iodo-1,3-dimethyl- | HCID 69097 | — |
| Edukt | Tri-o-tolylphosphine | HCID 80271 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | HCID 86631260 | HCID 86631260 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | (E)-9-(2,6-dimethylstyryl)-2-chloro-N-(4-(dimethylphosphoryl)phenyl)-9H-purin-6-amine | HCID 86631262 | — |
Reaktionsschritte
To an oven-dried 50 mL round-bottom flask were added 2-chloro-N-(4-(dimethylphosphoryl)phenyl)-9-vinyl-9H-purin-6-amine (0.32 g, 0.93 mmol), Pd(OAc)2 (10 mg, 0.05 mmol), tri-o-tolylphosphine (30 mg, 0.1 mmol), 2-iodo-m-xylene (0.39 g, 1.67 mmol). The mixture was flushed with Ar and then dissolved in ˜10 mL anhydrous DMF. DIEA (0.39 g, 2.79 mmol) was then added via syringe. The reaction was stirred at 110° C. overnight. The reaction was diluted with EtOAc and filtered through celite, washed with ample ˜5% MeOH/EtOAc, the combined organic layer was washed with water twice, dried over Na2SO4. Final product was purified by silica gel column chromatography (4˜8% MeOH/DCM).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08071609B2 |
|---|
| Quelldatensatz | uspto-grants-2011_12 |
|---|
| ORD ID | ord-5a886ae0e75c42aa984678b6579b604c |
|---|
| Quellennotiz | uspto-grants-2011_12 |
|---|