HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721589Generated: October 30, 2026
Thionyl Chloride → HCID 21890521, compound
https://huagongshe.com/reaction/721589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Bromothiophene-2-carboxylic acid | HCID 349115 | — |
| Reactant | 5-Bromothiophene-2-carbonyl chloride | HCID 605712 | — |
| Reactant | 4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2-methylaniline | HCID 21890510 | — |
| Reactant | HCID 21891177 | HCID 21891177 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21890521 | HCID 21890521 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135466B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-d3389d847f6143c386a6c975195b6a84 |
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| Source note | uspto-grants-2006_11 |
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