HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610285Generated: October 30, 2026
1-Methylpyrrolidine → 5-Amino-7-(3-aminoazetidin-1-yl)-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
https://huagongshe.com/reaction/610285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpyrrolidine | HCID 8454 | — |
| Reactant | Azetidin-3-amine--hydrogen chloride (1/2) | HCID 13491919 | — |
| Reactant | 5-Amino-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 22121165 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Amino-7-(3-aminoazetidin-1-yl)-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 22121191 | 23% |
Reaction Steps
To 550 mg of pyridine were added 185 mg of 5-amino-1- (6-amino-3 , 5-difluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, 110 mg of 3-aminoazetidine dihydrochloride, and 200 mg of N-methylpyrrolidine, and the mixture was stirred at 100° C. for 30 minutes, and concentrated under reduced pressure. After adding 2 ml of ethanol, the mixture was stirred, and the precipitate was collected by filtration and washed with ethanol and diisopropylether successively to obtain 48 mg of the title compound as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05998436 |
|---|
| Source dataset | uspto-grants-1999_12 |
|---|
| ORD ID | ord-ede23245d47f4a2ebdf5c9a0ba824ae2 |
|---|
| Source note | uspto-grants-1999_12 |
|---|