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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649456Generated: November 2, 2026

Trifluoroacetylpiperazine → 8-(4-trifluoroacetyl-1-piperazinyl)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid

https://huagongshe.com/reaction/1649456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetylpiperazineHCID 7172020—
Reactant8-(p-toluenesulfonyloxy)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acidHCID 20479743—
SolventDimethyl SulfoxideHCID 679—
Product8-(4-trifluoroacetyl-1-piperazinyl)-9-chloro-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acidHCID 1326952650%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04416884
Source datasetuspto-grants-1983_11
ORD IDord-d81ef5879557425d8886424787a1915e
Source noteuspto-grants-1983_11