Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178524722 | HCID 178524722 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178479697 | HCID 178479697 | — |
Reaction Steps
4-Hydroxy-1,5-naphthyridine-3-carboxylic acid was added to a mixture of benzene, 0.73 g of dimethylformamide and 1.56 g of thionyl chloride, and the resulting mixture was stirred at 40 to 85°C for 3 hours. The precipitated crystals were collected by filtration, washed with benzene and dried under reduced pressure to give 2.37 g of 4-hydroxyl-1,5-naphthyridine-3-carbonyl chloride hydrochloride as crystals. Purity (determined by NMR analysis as the ester from obtained by further alcoholysis), 96.3 %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03954733 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-6f040c532ad24e17aa0b4da4e7996ca0 |
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| Source note | uspto-grants-1976_05 |
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