HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721593Generated: October 30, 2026
Thionyl Chloride → HCID 21890302, compound
https://huagongshe.com/reaction/721593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2-Nitrophenyl)acetic acid | HCID 77337 | — |
| Reactant | o-Nitrophenylacetyl chloride | HCID 140956 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21890302 | HCID 21890302 | — |
Reaction Steps
Toluene (20 ml) and thionyl chloride (1 ml) were added to commercially available 2-(2-nitrophenyl)acetic acid (80 mg), and the mixture was heated at 100° C. for one hr. The solvent was removed by distillation, and 2-(2-nitrophenyl)ethanoyl isothiocyanate was prepared using the resultant 2-(2-nitrophenyl)ethanoyl chloride as a starting compound according to the description of the literature. 2-(2-Nitrophenyl)ethanoyl isothiocyanate thus obtained was dissolved in ethanol (1 ml) to prepare a solution. 3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]aniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 16 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/methanol for development to give the title compound (8 mg, yield 10%).
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-916c7574315c4e11821922763572e3f1 |
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| Source note | uspto-grants-2006_11 |
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