HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743644Generated: November 4, 2026
Potassium Hydroxide → HCID 19423741, compound
https://huagongshe.com/reaction/743644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 19423646 | HCID 19423646 | — |
| Product | HCID 19423741 | HCID 19423741 | 74.3% |
Reaction Steps
A suspension of 1.8 g of 8-(3-acetylamino-1-azetidinyl)-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydrobenzo[b][1,8]-naphthyridine in 40 cm3 of N aqueous potassium hydroxide is heated with stirring to a temperature in the region of 100° C. for 24 hours. After cooling to approximately 70° C., some slight insoluble matter is removed by filtration. At the same temperature, 40 cm3 of N methanesulphonic acid are added to the filtrate, and the precipitate formed is drained and washed with 3 times 20 cm3 of water at approximately 70° C. After recrystallization in 100 cm3 of dimethylformamide, 1.05 g of 8-(3-amino-1-azetidinyl)-7-fluoro-1-methylamino-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid are obtained in the form of a yellow solid, which decomposes at 315°-318° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05556861 |
|---|
| Source dataset | uspto-grants-1996_09 |
|---|
| ORD ID | ord-8a7e95fd4dcf4d90be49293f0fff3aa7 |
|---|
| Source note | uspto-grants-1996_09 |
|---|