Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Trifluoromethyl)aniline | HCID 9964 | — |
| Reactant | 5-Methyl-1,2-oxazole-4-carbonyl chloride | HCID 2759917 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Leflunomide | HCID 3899 | 86.2% |
Reaction Steps
4-Trifluoromethylaniline (5.75 g, 35.7 mm) was dissolved in a mixture of NaHCO3 (3.16 g, 37.6 mm), N,N-dimethylacetamide (0.7 ml, 7.5 mm) and toluene (70 ml). The mixture was warmed to 40° C. and 5-methylisoxazole-4-carboxylic acid chloride (5 g, 34.4 mm) was added dropwise over 20 min. The mixture was stirred at this temperature for another 3 h. and then it was heated to reflux temperature. The hot mixture was washed with water (3×10 ml). The organic phase was allowed to cool to ambient temperature, which induced leflunomide to precipitate as a white powder. The powder was isolated by filtration and then dried at 60° C. to give leflunomide (8.0 g, 86%) in 99.5% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06723855B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-cb0f6b5efcf3449cbd3b1a8808f4caef |
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| Source note | uspto-grants-2004_04 |
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