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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649446Generated: October 31, 2026

Piperazine → HCID 12836921, compound

https://huagongshe.com/reaction/1649446

Reaction equation

Participants

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

Reaction Steps

20 ml of dimethyl sulfoxide was 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 numberUS04416884
Source datasetuspto-grants-1983_11
ORD IDord-ba1e26ce1fa94436a5769126a052cae5
Source noteuspto-grants-1983_11