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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382210Generated: November 1, 2026

Ciprofloxacin → HCID 70393803, compound

https://huagongshe.com/reaction/1382210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCiprofloxacinHCID 2764—
ReactantAllyl bromideHCID 7841—
ReactantTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
ProductHCID 70393803HCID 7039380348.6%

Reaction Steps

3.3 g (10 mmol) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid are heated at 60° C. in 50 ml of dimethylformamide with 1.8 g (15 mmol) of allyl bromide and 2.1 g of triethylamine for 8 hours. The mixture is concentrated in vacuo, the residue is stirred with 30 ml of water and the precipitate is filtered off with suction, washed with methanol and dried. 2.2 g of 7-(4-allyl-1-piperazinyl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrobromide of melting point 295°-298° (with decomposition) are obtained; after recrystallization from water, 1.5 g of melting point 300°-302° (with decomposition) are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806539
Source datasetuspto-grants-1989_02
ORD IDord-296d4d4908354960bb47e32d59ca155c
Source noteuspto-grants-1989_02