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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721788Generated: October 31, 2026

Toluene → HCID 21890357, compound

https://huagongshe.com/reaction/721788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
Reactant4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-fluoroanilineHCID 11301470—
Reactant2,6-Dichlorobenzoyl isothiocyanateHCID 13798361—
SolventEthanolHCID 702—
Product2,6-Dichlorobenzoyl isothiocyanateHCID 13798361—
ProductHCID 21890357HCID 2189035782%

Reaction Steps

2,6-Dichloro-1-benzenecarbonyl isothiocyanate was prepared using commercially available 2,6-dichloro-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 2,6-Dichloro-1-benzenecarbonyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-fluoroaniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (71 mg, yield 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-29f291be635d4d52a9e027c27799958d
Source noteuspto-grants-2006_11