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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745659Generated: October 31, 2026

Hydrochloric Acid → HCID 13377054, compound

https://huagongshe.com/reaction/745659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantHCID 15571787HCID 15571787—
SolventDimethylformamideHCID 6228—
ProductHCID 13377054HCID 1337705460%

Reaction Steps

A mixture of 9-fluoro-6,7-dihydro-5-methyl-8-(1-piperazinyl)-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid (Compound [III]), hydrochloride (1.1 g), p-nitrobenzyl bromide (Compound [IV]) (1.87 g) and triethylamine (1.46 g) in N,N-dimethylformamide (50 ml) was heated with stirring at 80°-90° C. for 10 hr. After evaporation of the solvent, water was added to the residue, and the aqueous mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate and evaporated to dryness. The residue was recrystallized from a mixture of N,N-dimethylformamide and ethanol (2:1) to give 0.83 g (yield: 60%) of 8-[4-(4-nitrobenzyl)-1-piperazinyl]-9-fluoro-6,7-dihydro-5-methyl-1-oxo-1H, 5H-benzo[ij]quinolizine-2-carboxylic acid (Compound [II]) as pale yellow needles, m.p. 230°-233° C. (decompd.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04599418
Source datasetuspto-grants-1986_07
ORD IDord-0208913166824fd3b3cff771bf82c585
Source noteuspto-grants-1986_07