HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bicarbonate → 8-Cyano-1-cyclopropyl-7-[(1S,6S)-2-(5methyl-2-oxo-1,3-dioxol-4-yl)methyl-2,8-diazabicyclo[4.3.0]nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | Pradofloxacin | HCID 9802884 | — |
| Reactant | 4-(Bromomethyl)-5-methyl-1,3-dioxol-2-one | HCID 10774141 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Cyano-1-cyclopropyl-7-[(1S,6S)-2-(5methyl-2-oxo-1,3-dioxol-4-yl)methyl-2,8-diazabicyclo[4.3.0]nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid | HCID 70108425 | — |
Reaction Steps
100 mg (0.25 mmol) of 8-cyano-1-cyclopropyl-7-((1S,6S)-2,8-diazabicyclo[4.3.0]-nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 59 mg (0.30 mmol) of 4-bromomethyl-5-methyl-1,3-dioxol-2-one and 30 mg of potassium bicarbonate are heated at 140° C. in 2 ml of dimethylformamide for 30 minutes. The reaction solution is concentrated in vacuo, the residue is taken up in methylene chloride and the mixture is washed with water. The organic phase is dried over magnesium sulfate and concentrated in vacuo. The resulting residue is stirred with water, filtered off with suction and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06278013B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-b83e3be2654649b0a695f16018a44d6b |
| Source note | uspto-grants-2001_08 |