HuagongsheHuagongshe Chemistry Print Report · For research reference only
Norfloxacin → HCID 482669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Norfloxacin | HCID 4539 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Product | HCID 482669 | HCID 482669 | — |
Reaction Steps
1-Ethyl-6-fluoro-7-{4-[2-(4-chlorophenyl)-2-oxoethyl]-1-piperazinyl}-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid was prepared from norfloxacin (0.5 g, 1.56 mmole) and 2-bromo-4′-chloroaceto-phenone(0.43 g, 1.86 mmole) by a method similar to that described for Example 4 (67% yield). Mp: 207° C. (dec). 1H NMR (DMSO-d6) δ 1.41 (7, 3H, J=7.2), 2.73 and 3.29 (two m, 8H), 3.95 (s, 2H), 4.58 (q, 2H, J=7.2 7.19 (d, 1H, J=7.2), 7.59 and 8.02 (m, 4H), 7.92 (d, 1H, J=13.2), 8.95 (s, 1H), 15.41 (br s, 1H). Anal. Calcd. for C24H23ClFN3O4•0.25H2O: C, 60.51; H, 4.97; N, 8.82. Found: C, 60.49; H, 4.96; N, 8.82.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492373B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-80343a4dde814298a129ae1cb14148b5 |
| Source note | uspto-grants-2002_12 |