HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetylpiperazine → 8-(4-trifluoroacetyl-1-piperazinyl)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetylpiperazine | HCID 7172020 | — |
| Reactant | 8-(p-toluenesulfonyloxy)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid | HCID 20479743 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 8-(4-trifluoroacetyl-1-piperazinyl)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid | HCID 13269526 | 50% |
Reaction Steps
A mixture of 4.5 g of 8-(p-toluenesulfonyloxy)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid, 9.1 g of 1-trifluoroacetylpiperazine and 200 ml of anhydrous dimethyl sulfoxide was heated with stirring in an autoclave at 150° to 160° C. for 17 hours under nitrogen gas flow at a pressure of 10 atms. The reaction mixture was treated in the same manner as Example 73 to obtain 2.3 g of 8-(4-trifluoroacetyl-1-piperazinyl)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid as white rhombic crystals having a melting point of 300° C. or more.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04416884 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-d81ef5879557425d8886424787a1915e |
| Source note | uspto-grants-1983_11 |