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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721589Generated: October 30, 2026

Thionyl Chloride → HCID 21890521, compound

https://huagongshe.com/reaction/721589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-Bromothiophene-2-carboxylic acidHCID 349115—
Reactant5-Bromothiophene-2-carbonyl chlorideHCID 605712—
Reactant4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2-methylanilineHCID 21890510—
ReactantHCID 21891177HCID 21891177—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 21890521HCID 2189052165%

Reaction Conditions

Temperature100 °C

Reaction Steps

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 5-bromo-2-thiophenecarboxylic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 5-bromo-2-thiophene isothiocyanate was prepared using the resultant 5-bromo-2-thiophenecarbonyl chloride as a starting compound according to the description of the literature. 5-Bromo-2-thiophenecarbonyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-methylaniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 18 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 (58 mg, yield 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-d3389d847f6143c386a6c975195b6a84
Source noteuspto-grants-2006_11