HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenylhydrazine → HCID 178518862, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenylhydrazine | HCID 7516 | — |
| Edukt | Hydrazine | HCID 9321 | — |
| Edukt | Nicotinoyl chloride | HCID 82604 | — |
| Edukt | 1H-pyrazolo(3,4-b)pyridine | HCID 2755850 | — |
| Edukt | 2-Chloronicotinoyl chloride | HCID 2774541 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 178518862 | HCID 178518862 | — |
Reaktionsschritte
Scheme 4 depicts the synthesis of the 1H-pyrazolo[3,4-b]pyridine q. A nicotinoylchloride k (e.g., 2-chloronicotinoyl chloride) is reacted with a hydrazine m (e.g., phenylhydrazine) and a base such as triethylamine in a solvent such as anhydrous methylene chloride to give o (e.g., 1-phenyl-1H-pyrazolo[3,4-b]pyridin-3-ol). The compound o is then cyclized by heating at 175° C. to provide p. p is reacted as in the transformation of d to g in Scheme 1 to provide q.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07423054B2 |
| Quelldatensatz | uspto-grants-2008_09 |
| ORD ID | ord-92e1e1747f1e438698152e155671ed1e |
| Quellennotiz | uspto-grants-2008_09 |