Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,6-Octanedione | HCID 165054 | — |
| Reactant | HCID 12603548 | HCID 12603548 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 23275890 | HCID 23275890 | 85.7% |
Reaction Steps
To 1.95 g (10 m moles) of 3-hydrazino-6-morpholino-pyridazine dissolved in 12 ml of acetic acid, 1.71 g (12 m moles) of 3,6-octanedione dissolved in 4 ml of acetic acid are added at room temperature. The mixture is heated at 67° C. for 2 hours and then evaporated to dryness under vacuum. The oily residue is dissolved in toluene and the solution is evaporated to dryness. The residue is slurried with ice-water and neutralized with sodium bicarbonate to yield 2.58 g of a solid product. Said material, after crystallization from isopropanol gives 1.25 g (42%) of the title product, melting at 186°-9° C. Elemental analysis, I. R., N.M.R. and mass spectra are in agreement with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04247551 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-2577727d135a48c081c88daa4e556844 |
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| Source note | uspto-grants-1981_01 |
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