HuagongsheHuagongshe Chemistry Print Report · For research reference only
7,8-Difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid → HCID 19423673, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7,8-Difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid | HCID 11197026 | — |
| Reactant | 3-Methyl-3-(methylamino)azetidine dimethanesulphonate | HCID 19423736 | — |
| Product | HCID 19423673 | HCID 19423673 | — |
Reaction Steps
7-Fluoro-1-methyl-8-(3-methyl-3-methylamino-1-azetidinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]-naphthyridine-3-carboxylic acid was prepared under the conditions of Example 15, but starting with 1.45 g of 7,8-difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b]-[1,8]naphthyridine-3-carboxylic acid and 2.34 g of 3-methyl-3-(methylamino)azetidine dimethanesulphonate. The reaction mixture is heated for 1 and a half hours to approximately 90° C. 1.12 g of 7-fluoro-1-methyl-8-(3-methyl-3-methylamino-1-azetidinyl)-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid are obtained in the form of a yellow solid, which decomposes at approximately 336° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556861 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-7d6f0f5508794e00903aceff1c4a9a9c |
| Source note | uspto-grants-1996_09 |