HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tri(butyl)vinylstannane → Ethyl 1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-5-vinyl-3-quinolinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tri(butyl)vinylstannane | HCID 21115800 | — |
| Reactant | Ethyl 5-bromo-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate | HCID 22924353 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-5-vinyl-3-quinolinecarboxylate | HCID 22924366 | — |
Reaction Conditions
| Temperature | -18 °C |
|---|
Reaction Steps
5.9 g of ethyl 5-bromo-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate, 6.7 g of tributylvinylstannane and 0.69 g of tetrakis(triphenylphosphine)palladium(0) are refluxed for 10 hours in 60 ml of absolute toluene under a nitrogen atmosphere. The reaction mixture is cooled to -18° C., and the solid which has precipitated is filtered off with suction, washed with toluene and dried. 4.46 of the title compound are obtained (88% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05659038 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-e127c55241e2448e82fb6f9af52feb11 |
| Source note | uspto-grants-1997_08 |