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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898110Generated: October 31, 2026

Water → 6-[(2-Aminoethyl)amino]-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

https://huagongshe.com/reaction/898110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthylenediamineHCID 3301—
ReactantFluoroquinolonic acidHCID 483180—
SolventDimethylacetamideHCID 31374—
Product6-[(2-Aminoethyl)amino]-7-chloro-1-cyclopropyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 1798049410%

Reaction Conditions

Temperature115 °C

Reaction Steps

7-Chloro-1-cyclopropyl-1,4-dihydro-6-fluoro4-oxo-quinoline-3-carboxylic acid (56.3 g) and ethylenediamine (36 g) were dissolved in N,N-dimethylacetamide (650 mL) at 100° C. and stirred for 8.5 h at 115° C. Water (700 mL) was added to the reaction mixture cooled at room temperature. The reaction mixture was stirred at room temperature for 2 h, cooled at 0-5° C. and stirred for 1 h. The precipitate obtained was filtered, washed with cold water, cold EtOH, and dried at 110° C. under reduced pressure for 1 h. The crude product was treated with HCl (6% aqueous solution) heating for 1 h in the presence of charcoal. After filtration, the solution was cooled to 35-40° C. and a first precipitation happened. The precipitate was filtered, washed with water and dried at 110° C. for 1 h. The title compound (6.4 g) was obtained as the hydrochloride salt. The hydrochloride salt was then converted to the free base using standard conditions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351696B2
Source datasetuspto-grants-2008_04
ORD IDord-ad37b714cf6b4a51939c308075b4d8e7
Source noteuspto-grants-2008_04