Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 13345729 | HCID 13345729 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13345730 | HCID 13345730 | — |
Reaction Steps
A mixture of 11.5 g of ethyl 2,3-dihydro-3-methyl-7-oxo-10-phenyl-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylate and 75 ml of glacial acetic acid was heated to reflux temperature and 75 ml of 6 N hydrochloric acid was subsequently added. Refluxing was continued for one hour after which time 150 ml of water was added. The solution was cooled and filtered to provide light brown solid 2,3-dihydro-3-methyl-7-oxo-10-phenyl-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid, m.p. 295°-296° C. Recrystallization from aqueous N,N-dimethylformamide gave light yellow crystals. Analysis: Calculated for C19H15NO4 : %C, 71.0; %H, 4.7; %N, 4.4; Found: %C, 70.4; %H, 4.6; %N, 4.3. The structural assignment was confirmed by infrared and nuclear magnetic resonance spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04443447 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-4031e9a82bf549dabee976dd3257fea3 |
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| Source note | uspto-grants-1984_04 |
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