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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612013Generated: October 30, 2026

3-Aminobenzyl alcohol → HCID 9923792, compound

https://huagongshe.com/reaction/612013

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzyl alcoholHCID 80293—
Reactant1-EthoxyethanolHCID 10129898—
Reactant4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrileHCID 10586676—
SolventPyridineHCID 1049—
ProductHCID 9923792HCID 992379286%

Reaction Steps

A mixture of 1.0 g of 4-chloro-6,7-dimethoxy-3-quinolinecarbonitrile, 0.98 g of 3-aminobenzyl alcohol, 0.32 ml of pyridine, and 12 ml of ethoxyethanol was stirred, under nitrogen, at reflux temperature for 3 h. The mixture was cooled and partitioned with dichloromethane and aqueous sodium bicarbonate. The organic layer was washed with water, dried and evaporated. The residue was washed with hot methanol to give 1.16 g of 4-[(3-(hydroxymethyl)phenyl)amino]-6,7-dimethoxy-3-quinolinecarbonitrile as a solid, mp 250-255° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06002008
Source datasetuspto-grants-1999_12
ORD IDord-fb735e727db9469bb0778e23797efbbd
Source noteuspto-grants-1999_12