Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 10478140 | HCID 10478140 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10044403 | HCID 10044403 | — |
Reaction Steps
A mixture of 610 mg of ethyl 7-(4-acetyl-1-piperazinyl)-6-chloro-1-methyl-4-oxo-4H-(1,3)thiazeto(3,2-a)quinoline-3-carboxylate, 12 ml of 5% hydrochloric acid and 3 ml of ethanol was heated with stirring on an oil bath of 100°-110° C. for 2 hours. After cooling to about 50° C., this was neutralized with 5% ammonia water. Crystals separated out were collected by filtration, washed with water, dried and recrystallized from N,N-dimethylformamide to give pale yellow crystals, m.p. not lower than 300° C. (decompn).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04843070 |
|---|
| Source dataset | uspto-grants-1989_06 |
|---|
| ORD ID | ord-48d6301a79fc4da0aa48c3ea41a12dfd |
|---|
| Source note | uspto-grants-1989_06 |
|---|