Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 18994607 | HCID 18994607 | — |
| Product | HCID 14700561 | HCID 14700561 | — |
Reaction Steps
7-Fluoro-8-(4-methyl-1-piperazinyl)-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid is prepared under the conditions of Application Example 2, but starting with 0.3 g of 7-fluoro-1-methyl-8-(4-methyl-1-piperazinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxamide. After cooling to approximately 20° C., the reaction mixture is treated with 50 cm3 of water; the insoluble matter is drained and washed with twice 10 cm3 of water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05442070 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-c657066e69f04acb9ec0b1d983e7541e |
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| Source note | uspto-grants-1995_08 |
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