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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649457Generated: October 26, 2026

Hydrochloric Acid → 8-(4-trifluoromethyl-1-piperazinyl)-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid hydrochloride

https://huagongshe.com/reaction/1649457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant8-methanesulfonyloxy-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acidHCID 12899680—
Reactant1-(Trifluoromethyl)piperazineHCID 22717047—
SolventDimethyl SulfoxideHCID 679—
Product8-(4-trifluoromethyl-1-piperazinyl)-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid hydrochlorideHCID 70529582—

Reaction Steps

A mixture of 3.37 g of 8-methanesulfonyloxy-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid, 9.1 g of 1-trifluoromethylpiperazine and 200 ml of anhydrous dimethyl sulfoxide was heated with stirring in an autoclave at 170° to 180° C. for 20 hours under nitrogen gas flow at a pressure of 8 atms. The reaction mixture was treated in the same manner as in Example 73 and further treated with concentrated hydrochloric acid to obtain 1.7 g of 8-(4-trifluoromethyl-1-piperazinyl)-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid hydrochloride 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-b19115834d0f49b0983be4a0dc341bec
Source noteuspto-grants-1983_11