Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydrazinobenzoic acid | HCID 12089 | — |
| Reactant | 2-(2-Hydroxyphenyl)-4H-1,3-benzoxazin-4-one | HCID 135685723 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Trichloroacetic Acid | HCID 6421 | — |
| Product | Deferasirox | HCID 214348 | 55% |
Reaction Steps
A suspension of 0.7 g (2.92 mmol) of 2-(2-hydroxyphenyl)benz[e][1,3]oxazin-4-one and 0.52 g (3.44 mmol) of 4-hydrazinobenzoic acid in 5 g of trichloroacetic acid and 5 ml of toluene is heated to 110° C. The mixture is maintained and stirred at this temperature for 3 hours. After completion of the reaction, the mixture is cooled and poured onto crushed ice. The resulting crystals are aspirated and washed with water and ethyl acetate. After drying, 0.6 g of raw deferasirox is obtained, i.e. 55% of the theory, with an HPLC content of 99.56% and a melting temperature of 258 to 262° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129421B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-37518feb4b82461f84686015f36dc57a |
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| Source note | uspto-grants-2012_03 |
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