HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indazol-6-amine → HCID 21704767, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indazol-6-amine | HCID 81423 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10539447 | HCID 10539447 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21704767 | HCID 21704767 | 47.1% |
Reaction Steps
A mixture of 1.00 g (3.82 mmol) of 4-chloro-6-ethoxy-7-methoxyquinoline-3-carbonitrile and 0.609 g (4.58 mmol) of 6-aminoindazole in 20 mL of EtOH was refluxed under N2 for 8 h. Satd NaHCO3 was added, solvent was removed and the residue was azeotroped twice with EtOH. The solid was slurried with cold EtOH, collected, washed twice with H2O and dried. Recrystallization from EtOH yielded 0.646 g of 6-ethoxy-4-(1H-indazol-6-ylamino)-7-methoxyquinoline-3-carbonitrile as tan crystals: mass spectrum (electrospray, m/e): M+H 359.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288082B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-3ca157ae77884c71969ec745b86c5021 |
| Source note | uspto-grants-2001_09 |