HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884975Generated: October 26, 2026
Dimethylformamide → N-(5-tert-butyl-2-hydroxyphenyl)-3-fluoroisonicotinamide
https://huagongshe.com/reaction/884975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4-tert-butylphenol | HCID 70982 | — |
| Reactant | 3-Fluoroisonicotinoyl chloride | HCID 23287757 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(5-tert-butyl-2-hydroxyphenyl)-3-fluoroisonicotinamide | HCID 66880592 | — |
Reaction Steps
A mixture of 1.5 g of 3-fluoroisonicotinic acid, 5 ml of thionyl chloride and 50 mg of DMF was heated to reflux for two hours. The reaction mixture was cooled to room temperature, and then the reaction mixture was concentrated under reduced pressure to give 3-fluoroisonicotinic acid chloride. A mixture of the resultant 3-fluoroisonicotinic acid chloride and 5 ml of DMF was added dropwise to a mixture of 1.76 g of 2-amino-4-tert-butylphenol, 2.18 g of triethylamine and 10 ml of DMF while ice-cooling. The reaction mixture was stirred at room temperature for 1.5 hours and at 50° C. for 30 minutes. The reaction mixture was cooled to room temperature, and then water was added. Precipitated crystals were collected by filtration. The resultant crystals were dissolved in ethyl acetate, washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, concentrated under reduced pressure to give 2.41 g of N-(5-tert-butyl-2-hydroxyphenyl)-3-fluoroisonicotinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242133B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-faef342a950f4f35a03f8e5e9e2f5424 |
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| Source note | uspto-grants-2012_08 |
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