HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268316Generated: November 1, 2026
Dimethylformamide → 2H-Pyrido[4,3-d][1,3]oxazine-2,4(1H)-dione
https://huagongshe.com/reaction/268316
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-(Aminocarbonyl)-3-pyridinecarboxylic acid | HCID 1201428 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Product | 2H-Pyrido[4,3-d][1,3]oxazine-2,4(1H)-dione | HCID 10797096 | — |
Reaction Steps
A 50 ml. flask was charged with 2.6 g. lead tetra-acetate suspended in 10 ml. dimethylformamide and stirred while a solution of 0.96 g. of 4-carbamylnicotinic acid in 5 ml. dimethylformamide was added dropwise during 10 minutes. The mixture was stirred for 10 minutes after completion of the addition, then poured onto 40 g. crushed ice. A precipitate of cream solids was collected by filtration, washed with water and dried in vacuo. The yield of 5-azaisatoic anhydride amounted to 0.68 g., melting point 180° with decomposition, and represented 72 percent of theory. On attempted purification by crystallization from organic solvents, extensive decomposition occurred. The structure was confirmed by elemental analysis, infra-red spectroscopy and mass spectrometry.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03947416 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-5388b720fde34ecca7b9a30e63f0c943 |
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| Source note | uspto-grants-1976_03 |
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