HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477856Generated: October 31, 2026
Sodium Iodide → 1-Ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[2-(1-pyrrolidinylmethyl)morpholino]quinoline-3-carboxylic acid
https://huagongshe.com/reaction/477856
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 7-(2-Chloromethylmorpholino)-1-ethyl-6,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 14652631 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[2-(1-pyrrolidinylmethyl)morpholino]quinoline-3-carboxylic acid | HCID 14652632 | — |
Reaction Steps
A mixture of 397 mg of 7-(2-chloromethylmorpholino)-1-ethyl-6,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, 156 mg of pyrrolidine, 150 mg of sodium iodide and 15 ml of dimethylformamide is stirred at 150° C. for 7 hours. The reaction mixture is concentrated under reduced pressure and to the residue is added water followed by extracting with chloroform. The organic layer is washed with water, dried over anhydrous magnesium sulfate and then the solvent is distilled off to give 1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[2-(1-pyrrolidinylmethyl)morpholino]quinoline-3-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04889857 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-be0c3dbdce244c3dbed9a9d058a6f0ed |
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| Source note | uspto-grants-1989_12 |
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