Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Oxcarbazepine | HCID 34312 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57087814 | HCID 57087814 | — |
Reaction Steps
A mixture of 0.2 g (0.8 mmol) of 10,11-dihydro-10-oxo-5H-dibenz[b,f]azepine-5-carboxamide, 0.5 g (4.6 mmol) of phenylhydrazine and 0.5 g (6 mmol) of sodium acetate in a mixture of 5 mL of water, 5 mL of ethanol and 3 drops of concentrated hydrochloric acid was heated at 60° C. for thirty minutes and then allowed to cool to room temperature. The precipitate was then filtered and washed with cold water and dilute ethanol to give the desired product as yellow crystals of m.p. 220° to 220.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866566 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-855a5c958cf4417daab61cf5df6532a4 |
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| Source note | uspto-grants-1999_02 |
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