HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 4-Methoxy-1H-pyrrolo(2,3-c)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 5,7-Dibromo-4-methoxy-6-azaindole | HCID 22476267 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methoxy-1H-pyrrolo(2,3-c)pyridine | HCID 22476237 | 88% |
Reaction Steps
A solution of 5,7-Dibromo-4-methoxy-6-azaindole 36 (680 mg, 2.22 mmol), 5% Pd/C (350 mg, 0.17 mmol) and hydrazine (2.5 mL, 80 mmol) in EtOH was heated at reflux for 1 h. The reaction mixture was allowed to cool to rt, filtered through celite and the filtrate concentrated. Aqueous NH4OH (11% in H2O, 45 mL) was added to the residue and the solution was extracted with CH2Cl2 (3×30 mL). The combined organics were dried (MgSO4), filtered and concentrated to yield 4-methoxy-6-azaindole 37 (290 mg, 1.95 mmol, 88%) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06632819B1 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-936d3f1a1f804cb3b7a652cf16e150df |
| Source note | uspto-grants-2003_10 |