HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(6-Fluoroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(3-Chloro-6-fluoro-3,4-dihydroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil | HCID 19025383 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(6-Fluoroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil | HCID 19025385 | 97.4% |
Reaction Steps
A stirred solution of 5.2 grams (0.013 mole) of 3-(3-chloro-6-fluoro-3,4-dihydroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil and 6.2 grams (0.061 mole) of triethylamine in 200 mL of tetrahydrofuran was concentrated under reduced pressure to a residue. The residue was dissolved in methylene chloride and washed with water. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 4.5 grams of 3-(6-fluoroquinolin-2-on-7-yl)-1-methyl-6-trifluoromethyluracil, mp 179° C., dec. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05310723 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-111766c06f1c49099b4d4be7a08e703c |
| Source note | uspto-grants-1994_05 |