Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663077Generated: October 29, 2026

Anthranilic Acid → HCID 67132180, compound

https://huagongshe.com/reaction/1663077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnthranilic AcidHCID 227—
Reactant4-QuinolinecarboxaldehydeHCID 78072—
SolventMethanolHCID 887—
ProductHCID 67132180HCID 6713218093.9%

Reaction Steps

A solution of anthranilic acid (5.46 g) in methanol was added to a melt of quinoline-4-carbaldehyde (6.26 g) and the mixture was heated on a water bath for 6 hours. The mixture was cooled to room temperature and the solid material was isolated by filtration and washed with methanol, affording 2-[(quinolin-4-ylmethylene)-amino]-benzoic acid (10.33 g). This intermediate (10.3 g) was dissolved in THF and ethanol, and sodium borohydride (1.41 g) was added portion-wise. The reaction mixture was stirred at room temperature for 3 hours. More sodium borohydride (1.41 g) and a small amount of methanol were added and stirring continued at room temperature for 4 hours. The mixture was evaporated under reduced pressure and transferred to a separatory funnel with EtOAc and water. Layers were separated and the aqueous layer was neutralised by addition of 4M hydrochloric acid. The resulting precipitated material was isolated by filtration, washed with water and dried in vacuo, affording the title compound (7.1 g). 13C-NMR (DMSO-d6) δ 170.4, 150.3, 150.3, 147.6, 144.8, 133.4, 131.7, 129.6, 129.2, 126.5, 126.1, 123.5, 118.5, 114.6, 112.9, 111.2, 42.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034811B2
Source datasetuspto-grants-2011_10
ORD IDord-a93304be12bd4b53833ed2341a8da468
Source noteuspto-grants-2011_10