HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599363Generated: October 31, 2026
Triethylamine → 2-(Quinolin-4-ylmethylthio)-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamide
https://huagongshe.com/reaction/599363
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-(Chloromethyl)quinoline | HCID 12355701 | — |
| Reactant | 2-mercapto-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamide | HCID 178522235 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Quinolin-4-ylmethylthio)-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamide | HCID 11847044 | 52% |
Reaction Steps
Triethylamine (66 μL, 0.47 mmol) was added to a solution of 2-mercapto-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamide (Reference Compound No. 8-3, 52 mg, 0.17 mmol) and 4-(chloromethyl)quinoline (Reference Compound No. 5-1, 28 mg, 0.16 mmol) in anhydrous N,N-dimethylformamide (11.0 mL) at room temperature, and the mixture was stirred for 18 hours. Ethyl acetate (50 mL) was added thereto, then the whole was washed with saturated aqueous sodium hydrogencarbonate solution (5 mL) and brine (50 mL). The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and then the resulting residue was purified by silica gel column chromatography to give 40 mg of the title compound as a white amorphous (Yield: 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897774B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-ce95029d13354666ae5c0ec456e1fa88 |
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| Source note | uspto-grants-2011_03 |
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