HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242032Generated: October 31, 2026
Lawesson's reagent → HCID 86662687, compound
https://huagongshe.com/reaction/242032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 66776512 | HCID 66776512 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86662687 | HCID 86662687 | 82% |
Reaction Steps
A solution of 460 mg (1.5 mmol) ethyl 1,4-dimethyl-2-oxo-7-(trifluoromethyl)-1H-quinoline-3-carboxylate in toluene (10 ml) was treated with 2.4 g (5.9 mmol) Lawesson's reagent at RT, followed by heating to 120° C. for 16 h. After cooling to RT the RS was quenched with a sat. aq. Na2CO3 solution (30 ml). The mixture was then extracted with EtOAc (3×30 ml). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo. CC (EtOAc/hexane 1:4) of the residue provided 400 mg (1.2 mmol, 82%) ethyl 1,4-dimethyl-2-thioxo-7-(trifluoromethyl)-1H-quinoline-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653102B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-0ac1a85a87bc4dc4af7c4976d4defeca |
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| Source note | uspto-grants-2014_02 |
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