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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595767Generated: October 26, 2026

1H-Indazol-6-amine → 7-Ethoxy-4-(indazol-6-ylamino)-6-methoxy-quinoline-3-carbonitrile

https://huagongshe.com/reaction/1595767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indazol-6-amineHCID 81423—
Reactant4-Chloro-7-ethoxy-6-methoxy-3-quinolinecarbonitrileHCID 10563473—
SolventEthanolHCID 702—
Product7-Ethoxy-4-(indazol-6-ylamino)-6-methoxy-quinoline-3-carbonitrileHCID 1029194080%

Reaction Steps

A mixture of 500 mg (1.90 mmol) 4-chloro-7-ethoxy-6-methoxy-quinoline-3-carbonitrile, 30 ml ethanol, and 304 mg (2.28 mmol) 6-aminoindazole was heated to reflux under N2. Removed heat at 4 hours and made basic with saturated sodium bicarbonate. Stripped solvents, slurried residue with hexane, collected solids and dried. Washed with water and dried in vacuo, giving 546 mg of tan solid: mass spectrum (electrospray m/e): M+H=359.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288082B1
Source datasetuspto-grants-2001_09
ORD IDord-159ba4eba5f34f4c8b7c149474b0e620
Source noteuspto-grants-2001_09