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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058505Generated: October 30, 2026

Piperazine → HCID 12836921, compound

https://huagongshe.com/reaction/2058505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 12836918HCID 12836918—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 12836921HCID 1283692137.2%

Reaction Steps

20 ml of dimethyl sulfoxide were added to a mixture of 3 g of 9-chloro-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid and 6 g of anhydrous piperazine and the mixture was heated on an oil bath at 140° to 150° C. for 6 hours. After completion of reaction, the solvent was removed therefrom under reduced pressure and 50 ml of water was added to the residue to dissolve it. The solution was shaken with 100 ml of chloroform and the water layer was separated and treated with activated carbon. The aqueous solution was rendered acidic with a 10% aqueous hydrochloric acid and filtered. The filtrate was again treated with activated carbon followed by concentration. The addition of ethanol to the concentrate gave rise to crystals which were recrystallized from ethanol-water to obtain 1.5 g of 9-(1-piperazinyl)-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid hydrochloride as light yellow needles having a melting point of 300° C. or more.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04317820
Source datasetuspto-grants-1982_03
ORD IDord-a363df6095454a7c9f68b305254f65ff
Source noteuspto-grants-1982_03