HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → HCID 178518862, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Nicotinoyl chloride | HCID 82604 | — |
| Reactant | 1H-pyrazolo(3,4-b)pyridine | HCID 2755850 | — |
| Reactant | 2-Chloronicotinoyl chloride | HCID 2774541 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178518862 | HCID 178518862 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485636B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-04791b4fb7df49afb20a6caf7d8afbb9 |
| Source note | uspto-grants-2009_02 |