Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721816Generated: October 30, 2026

Thionyl Chloride → HCID 58738975, compound

https://huagongshe.com/reaction/721816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-Methylthiophene-2-carboxylic acidHCID 74713—
Reactant5-Methylthiophene-2-carbonyl chlorideHCID 2760083—
Reactant4-((6,7-Dimethoxyquinolin-4-yl)oxy)-3-fluorobenzenamineHCID 11426997—
ReactantHCID 21890540HCID 21890540—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 58738975HCID 5873897562%

Reaction Conditions

Temperature100 °C

Reaction Steps

Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 5-methyl-2-thiophenecarboxylic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 5-methyl-2-thiophenecarbonyl isothiocyanate was prepared using the resultant 5-methyl-2-thiophenecarbonyl chloride as a starting compound according to the description of the literature. 5-Methyl-2-thiophenecarbonyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-3-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 (49 mg, yield 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-12d3af0f77724fc78f0deff8fc73bd81
Source noteuspto-grants-2006_11