HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 13116432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | N-Piperidinoethanol | HCID 18232 | — |
| Reactant | 8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)quinoline-4-carboxylic acid | HCID 10470045 | — |
| Product | HCID 13116432 | HCID 13116432 | — |
Reaction Steps
A mixture of 500 mg (1.67 mmol) of 8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylic acid and 1.09 grams (8.34 mmol) of N-(beta-hydroxyethyl)-piperidine was suspended in 20 ml of pyridine and the mixture was heated to reflux for thirty two hours. When the reaction was completed, the mixture was cooled to a room temperature, crystals separated out therefrom were collected by filtration, successively washed with pyridine, ethanol and ether, and recrystallized from dimethyl formamide to give the title compound as pale yellow powders. Yield 426.6 mg (65 percent). Melting point 256° to 256.5° C. Elementary analysis calculated as C18H20FN3O4S: C 54.95, H 5.12, N 10.68; Found: C 54.52, H 5.14, N 10.73.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04426381 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-c70ba637521f4d6894b515cfa00e7864 |
| Source note | uspto-grants-1984_01 |