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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284524Generated: October 26, 2026

Ciprofloxacin → 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-{4-[2-oxo-1-(methoxycarbonyl)-1-propyl]-1-piperazinyl}-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/1284524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCiprofloxacinHCID 2764—
ReactantTriethylamineHCID 8471—
ReactantMethyl 2-chloroacetoacetateHCID 107332—
SolventDimethylformamideHCID 6228—
Product1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-{4-[2-oxo-1-(methoxycarbonyl)-1-propyl]-1-piperazinyl}-3-quinolinecarboxylic acidHCID 1333793144%

Reaction Steps

6.6 g (0.02 mole) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid are heated at 80° C. with 4.5 g of methyl 2-chloroacetoacetate and 4.2 g of triethylamine in 100 ml of dimethylformamide for 3 hours. The solution is then concentrated in vacuo, the residue is stirred with 50 ml of water and the resulting solid product is washed with methanol and water and recrystallized from glycol monomethyl ether. 3.9 g (44% of theory) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-{4-[2-oxo-1-(methoxycarbonyl)-1-propyl]-1-piperazinyl}-3-quinolinecarboxylic acid of decomposition point 224° to 228° C. are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563448
Source datasetuspto-grants-1986_01
ORD IDord-47d429a7435e48fda8e9b2d108dfdb70
Source noteuspto-grants-1986_01