HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 54717980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 54710916 | HCID 54710916 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54717980 | HCID 54717980 | — |
Reaction Steps
A mixture of 2 parts of N-(4-aminophenyl)-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide, 5 parts of pyridine, and 10 parts of acetic anhydride is left overnight at room temperature. Water is added and the precipitate is filtered off and washed with 2M aqueous hydrochloric acid, water, methanol and ethylether to give N-(4-acetylaminophenyl)-1,2-dihydro-4-hydroxy-1-methyl-2-oxo-quinoline-3-carboxamide (1). M.p. 231°-4° C. (The same compound as 1:41.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04738971 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-92b741763fef4406a5df0885e8688c9b |
| Source note | uspto-grants-1988_04 |