Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | HCID 19783732 | HCID 19783732 | — |
| Reactant | HCID 20149300 | HCID 20149300 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 10668222 | HCID 10668222 | 62% |
Reaction Steps
To a solution of 3.36 g of 7 chloro-1-p-fluoro-phenyl-6-fluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid (the product of Example 4(b)) in 35 ml of 1-methyl-2-pyrrolidinone at 115° C. is added 4.13 g of thiomorpholine. After stirring at 115° C. for 20 hours, the solvent is removed by reduced pressure to dryness. Methanol is added to the residue and the resulting mixture is filtered and washed with ethylacetate and then washed with water. The solid is dried, yielding 2.51 g 1-p-fluorophenyl-6-fluoro-1,4-dihydro-4-oxo-7-thiomorpholino-quinoline-3-carboxylic acid (9) ##STR36## R=p-fluorophenyl) in 62% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04730000 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-2acc54ceb1b845af845fec96aaba23d9 |
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| Source note | uspto-grants-1988_03 |
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