Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Daunorubicin Hydrochloride | HCID 62770 | — |
| Reactant | p-Phenylbenzhydrazide | HCID 72718 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Daunorubicin | HCID 30323 | 111.3% |
Reaction Steps
A solution of 1.13 g (2.0 mmole) of daunomycin hydrochloride and 0.85 g (4.0 mmole) of 4-phenylbenzhydrazide in 75 ml of methanol was stirred at room temperature in the dark for 4 days. After concentrating to about 10 ml, the reaction mixture was stirred and slowly diluted with 100 ml of acetonitrile. The resulting precipitate was collected and washed with 3 × 5 ml of acetonitrile to afford 1.174 g of the hydrazone (I) with a small amount of 4-phenylbenzhydrazide. The mother liquors were evaporated; the residue was dissolved in 5 ml of methanol and the stirred solution was diluted with 75 ml of acetonitrile to give an additional 0.211 g of (I). The two crops of (I) were combined and dissolved in 5 ml of methanol; the solution was stirred and 75 ml of acetonitrile were added dropwise. The resulting precipitate was triturated in the methanol-acetonitrile mixture overnight and then collected, washed with acetonitrile and dried at room temperature/0.1 mm/15 hr to yield the hydrazone hydrochloride (I), 1.253 g (81%) mp 205°-208° decomposed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04125704 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-ad62024268224c8d916ae96891917c00 |
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| Source note | uspto-grants-1978_11 |
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