Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylaniline | HCID 7515 | — |
| Reactant | HCID 54710203 | HCID 54710203 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 54710169 | HCID 54710169 | — |
Reaction Steps
A mixture of 2,3-dihydro-6-ethoxycarbonyl-7-hydroxy-5-oxo-5H-pyrido[1,2,3-de]-1,4-benzoxazine (6 g) and N-methylaniline (4 ml) in pyridine (30 ml) was stirred at 125° C. for 4 hours. The solvent was evaporated, and the residue was purified by column chromatography on silica gel (200 g) eluting with a mixture of chloroform and methanol (5:1). The product was recrystallized from a mixture of ethanol and isopropyl ether to give pale brown crystals of 2,3-dihydro-7-hydroxy-6-(N-methyl-N-phenylcarbamoyl)-5-oxo-5H-pyrido[1,2,3-de]-1,4-benzoxazine (1.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05583135 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-1347d8f94e9f4b19a525bb93aad0d3a8 |
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| Source note | uspto-grants-1996_12 |
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