Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178469573 | HCID 178469573 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178515215 | HCID 178515215 | — |
Reaction Steps
To a slurry of 1.5 g of ethyl 4-hydroxy-1,5-naphthyridine-3-carboxylate (prepared according to J. Inorg. Nucl. Chem., (1966) 28, 2439) in 17 ml of dimethylformamide is added 0.907 g of oxalyl chloride in 2 ml of methylene chloride while maintaining the reaction temperature between -25° and -30°. The mixture is stirred at -25° for 35 minutes. A solution of 0.995 g of diisopropylethylamine and 0.833 g of phenylhydrazine in 4 ml of methylene chloride is added to the mixture in 8 minutes at -30° to -25°. The mixture is then stirred for 30 minutes at -25°, 20 minutes at 0° and 40 minutes at 23°. The resultant dark purple solution is poured into 60 ml of water. Dark precipitate is collected, washed with water and crystallized from methanol to yield 2-phenyl-pyrazolo[4,3-c] [1,5]naphthyridin-3(5H)-one, m.p. 314°-316°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04479955 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-4054b2332f69434db1d2e76cc3c223ea |
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| Source note | uspto-grants-1984_10 |
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