HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161797Generated: October 29, 2026
Sodium Azide → Methyl 7-fluoro-6-(2-fluorophenylamino)-3-methylbenzo[c]isoxazole-5-carboxylate
https://huagongshe.com/reaction/1161797
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Methyl 5-acetyl-2-(2-fluorophenylamino)-3,4-difluorobenzoate | HCID 59519431 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 7-fluoro-6-(2-fluorophenylamino)-3-methylbenzo[c]isoxazole-5-carboxylate | HCID 59519479 | 89% |
Reaction Steps
To a solution of methyl 5-acetyl-3,4-difluoro-2-(2-fluorophenylamino)benzoate (example 3, step D) (1.50 g, 4.64 mmol) in a mixture of acetone (36 ml) and H2O (12 ml) was added NaN3 (452 mg, 6.96 mmol). The reaction was heated at 65° C. for 16 h and cooled to room temperature. Acetone was concentrated and the resulting mixture was extracted with EtOAc (2×50 ml). The combined organic solution was washed with brine (50 ml), dried over MgSO4 and concentrated to give a yellow solid. To the solid was added H2O (24 ml) and the reaction was heated at reflux for 3 h. The reaction was cooled to room temperature, filtered, and washed with H2O. The resulting solid was dried under high vacuum with P2O5 at 65° C. for 24 h to give 1.31 g (89%) of methyl 7-fluoro-6-(2-fluorophenylamino)-3-methylbenzo[c]isoxazole-5-carboxylate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820664B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-b37c440abe2f4301a5f2ad73e1d3bcec |
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| Source note | uspto-grants-2010_10 |
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