HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408076Generated: October 31, 2026
Sodium ethanethiolate → HCID 66586843, compound
https://huagongshe.com/reaction/1408076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethanethiolate | HCID 4459711 | — |
| Reactant | N-(3-(trifluoromethyl)benzyl)-2-(5-fluoro-2-nitrophenyl)-isonicotinamide | HCID 66586802 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 66586843 | HCID 66586843 | — |
Reaction Steps
Into a 50-mL round-bottom flask, was placed a solution of N-(3-(trifluoromethyl)benzyl)-2-(5-fluoro-2-nitrophenyl)isonicotinamide 14d (300 mg, 0.72 mmol, 1.00 equiv) in DMSO (5 mL), and sodium ethanethiolate (100 mg, 1.19 mmol, 1.70 equiv). The resulting solution was stirred for overnight at 90° C. in an oil bath. The mixture was concentrated under vacuum. The residue was diluted with 20 mL of water. The resulting solution was extracted with 3×20 mL of dichloromethane and the organic layers combined. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 300 mg (crude) of N-(3-(trifluoromethyl)benzyl)-2-(5-(ethylthio)-2-nitrophenyl)isonicotinamide as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916569B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-d91106982886453fb464c891026b95a1 |
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| Source note | uspto-grants-2014_12 |
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