HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2041907Erstellt: 25. Oktober 2026
Tri-o-tolylphosphine → N-[3-[2-[6-(Methylamino)-9H-purine-9-yl]ethenyl]-4-methylphenyl]-3-(trifluoromethyl)benzamide
https://huagongshe.com/reaction/2041907
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tri-o-tolylphosphine | HCID 80271 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamide | HCID 7925506 | — |
| Edukt | N-Methyl-9-vinyl-9H-purin-6-amine | HCID 23649897 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[3-[2-[6-(Methylamino)-9H-purine-9-yl]ethenyl]-4-methylphenyl]-3-(trifluoromethyl)benzamide | HCID 15950818 | — |
Reaktionsschritte
A pressure tube was charged with N-methyl-9-vinyl-9H-purin-6-amine (0.088 g, 0.5 mmol), N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamide (0.20 g, 0.5 mmol), palladium acetate (0.05 eq), tri-(o-tolyl)phosphine (0.1 eq), and DMF (2 ml). The resulting solution was degassed by bubbling N2 for 10 minutes. N,N-Diisopropylethylamine (0.19 g, 1.5 mmol) was added and this solution was stirred at 110° C. for 15 h. Water was added and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated on a rotavap, and then subjected to silica gel column chromatography (5% methanol/methylene chloride) yielding the desired product: MS [M+H]+ 453; m.p. 201° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08586566B2 |
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| Quelldatensatz | uspto-grants-2013_11 |
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| ORD ID | ord-62350654f5e4425d9b448548233f3017 |
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| Quellennotiz | uspto-grants-2013_11 |
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