HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038433Generated: October 25, 2026
N-(3-Aminophenyl)-1-phenylmethanesulfonamide → 1-phenyl-N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide
https://huagongshe.com/reaction/1038433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(3-Aminophenyl)-1-phenylmethanesulfonamide | HCID 16772451 | — |
| Reactant | 2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazole | HCID 71060395 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-phenyl-N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide | HCID 71060466 | — |
Reaction Steps
A mixture of 2-chloro-5-(4-(trifluoromethyl)phenyl)oxazole 31 (0.651 g, 2.63 mmol) and N-(3-aminophenyl)-1-phenylmethanesulfonamide 26 (0.69 g, 2.63 mmol) in 2-propanol (50 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide 1-phenyl-N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide. 34 (0.407 g, 33% yield) as a solid. MS (ES) m/z 474 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551992B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-a8ab3eb49e8045ffb5fd057807149178 |
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| Source note | uspto-grants-2013_10 |
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