Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595775Generated: November 2, 2026

1H-Indazol-6-amine → HCID 9841012, compound

https://huagongshe.com/reaction/1595775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indazol-6-amineHCID 81423—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 10634199HCID 10634199—
SolventEthanolHCID 702—
ProductHCID 9841012HCID 984101275.9%

Reaction Steps

A mixture of 1.00 g (4.07 mmol) of 9-chloro-2,3-dihydro[1,4]dioxino[2,3-g]quinoline-8-carbonitrile and 0.649 g (4.88 mmol) of 6-aminoindazole in 25 mL of EtOH was refluxed under N2 for 5.7 h. Satd NaHCO3 was added and the solvent was removed. The residue was slurried with H2O, filtered, washed with H2O and cold EtOH and dried. The crude product was boiled with EtOH, filtered and dried in vacuo (50° C.) to yield 1.06 g of 9-(1H-indazol-6-ylamino)-2,3-dihydro[1,4]dioxino[2,3-g]quinoline-8-carbonitrile as tan crystals: mass spectrum (electrospray, m/e): M+H 344.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288082B1
Source datasetuspto-grants-2001_09
ORD IDord-6a4189d5589743aa9d40d3d70939bb0f
Source noteuspto-grants-2001_09