Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoniazid | HCID 3767 | — |
| Reactant | HCID 178467321 | HCID 178467321 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | HCID 178465645 | HCID 178465645 | 84.5% |
Reaction Steps
20.3 g of 3-acetyl-2,4-dihydroxyquinoline and 13.8 g of isonicotinic acid hydrazide are condensed in 180 ml of ethyl cellosolve analogously to Example 1, yielding 27.2 g of 3-acetyl-2,4-dihydroxyquinoline isonicotinoylhydrazone. 3.2 g of this product are suspended in 25 ml of dimethylformamide and treated with a solution of 2.7 g of nickel(II) acetate·4H2O in dimethylformamide. The resulting mixture is stirred for 2 hours at 80°-90° C. and the product is then isolated by filtration and subsequently washed with isopropanol and then with water. After the product has been dried under vacuum at 70°-80° C., 3.5 g of a yellow powder of the following formula: ##STR23## as the 1:1 nickel complex, are obtained which gives the following microanalysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05066695 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-a8fe6c371e79460f915b6288784ba7c8 |
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| Source note | uspto-grants-1991_11 |
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