Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637928Generated: October 31, 2026

Hydrochloric Acid → 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-{4-[(3-methoxycarbonylpropyl)-carbamoyl]-piperazin-1-yl}-quinoline-3-carboxylic acid

https://huagongshe.com/reaction/637928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCiprofloxacinHCID 2764—
ReactantMethyl 4-isocyanatobutanoateHCID 2759393—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
Product1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-{4-[(3-methoxycarbonylpropyl)-carbamoyl]-piperazin-1-yl}-quinoline-3-carboxylic acidHCID 1334021163.2%

Reaction Steps

6.6 g (0.02 mol) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(piperazin-1-yl)-quinoline-3-carboxylic acid are dissolved in a solution of 0.4 g of sodium hydroxide in 40 ml of water, and a solution of 3.2 g (0.022 mol) of methyl 4-isocyanato-butyrate in 12 ml of dioxane is added, while cooling with ice. Thereafter, stirring is continued for 2 hours at room temperature, the pH is adjusted to 5 with 2N hydrochloric acid and the precipitate is filtered off under suction and recrystallised from methanol. 6 g (63% of theory) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-{4-[(3-methoxycarbonylpropyl)-carbamoyl]-piperazin-1-yl}-quinoline-3-carboxylic acid of melting point 198°-200° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559341
Source datasetuspto-grants-1985_12
ORD IDord-c553ee97ffc64e9a8cd039de1d3ab2c3
Source noteuspto-grants-1985_12