HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → Ethyl 6,7-difluoro-1-(2-fluoroethyl)-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20067124 | HCID 20067124 | — |
| Product | Ethyl 6,7-difluoro-1-(2-fluoroethyl)-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate | HCID 20067126 | 24.8% |
Reaction Steps
A mixture of the whole (0.0022 mole) of the 3,4-difluoro-N-(2-fluoroethyl)-2-methoxyaniline prepared as described in step (C3) and 0.57 g (0.0026 mole) of diethyl ethoxymethylenemalonate was heated at 140°-150° C. for 6 hours, after which it was allowed to cool to room temperature. 2 ml of acetic anhydride and 1 ml of concentrated sulfuric acid were added in that order to the mixture, and it was then allowed to stand at room temperature. The reaction mixture was then poured into ice-water to precipitate crystals, which were collected by filtration to give 0.18 g of ethyl 6,7-difluoro-1-(2-fluoroethyl)-8-methoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate (X, R9' =2-fluoroethyl) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997943 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-e9c73ec8742646689a09ef251a4ae11b |
| Source note | uspto-grants-1991_03 |