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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434566Generated: October 30, 2026

Allyl bromide → HCID 12770911, compound

https://huagongshe.com/reaction/434566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTriethylamineHCID 8471—
ReactantHCID 12770893HCID 12770893—
SolventDimethylformamideHCID 6228—
ProductHCID 12770911HCID 1277091130.3%

Reaction Steps

A mixture of 1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)quinoline-3carboxylic acid hydrochloride (0.18 g), triethylamine (0.12 g), allyl bromide (0.09 g), and DMF (3 ml) was heated with stirring at 90° for 3 hours and the solvent was evaporated. The residue was dissolved in 2N sodium hydroxide solution. The alkaline solution was adjusted to pH 7 with aqueous acetic acid and extracted with dichloromethane. The organic layer was washed with water, dried over anhydrous sodium sulfate, and evaporated. The residue was recrystallized from a mixture of DMF and ethanol to give 7-(4-allyl-1-piperazinyl)-1-ethyl-6,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (0.055 g), mp 227°-230° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04398029
Source datasetuspto-grants-1983_08
ORD IDord-df06e0da7e5a4fd19395ad74c2b33431
Source noteuspto-grants-1983_08