HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzodiazepine → N-methylbenzodiazepine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzodiazepine | HCID 134664 | — |
| Edukt | Methyl iodide sodium hydride | HCID 23686416 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Produkt | N-methylbenzodiazepine | HCID 12543525 | — |
Reaktionsschritte
The bromide 20 available from references 9 and 10 was reacted with trimethylsilyacetylene in the presence of a palladium catalyst to provide trimethylsilyl analog 52. This product was methylated with methyl iodide/sodium hydride to give the N-methyl benzodiazepine 54 (XLi 351). This was subjected to fluoride-mediated desilation to furnish 53 (XLi 350) and 55 (XLi 352).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08835424B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-1b3beb3ba5df4868b8f6774c959dce1a |
| Quellennotiz | uspto-grants-2014_09 |