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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073618Generated: November 2, 2026

1-Ethylpiperazine → 1-Cyclopropyl-8-(4-ethyl-1-piperazinyl)-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/1073618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-EthylpiperazineHCID 79196—
Reactant8-Chloro-1-cyclopropyl-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700556—
SolventPyridineHCID 1049—
Product1-Cyclopropyl-8-(4-ethyl-1-piperazinyl)-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acidHCID 1470057627.2%

Reaction Steps

The reaction is carried out under the conditions of Reference Example 5 but starting from 2 g of 8-chloro-1-cyclopropyl-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid and 2.74 g of 1-ethylpiperazine in 20 cm, of pyridine. The pure product is isolated after a first recrystallization from 105 cm3 of ethanol containing 25% of dimethylformamide followed by a second recrystallization from 75 cm3 of ethanol containing 50% of dimethylformamide. 0.67 g of 1-cyclopropyl-8-(4-ethyl-1-piperazinyl)-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid is obtained in the form of a yellow-green solid melting at 254° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970213
Source datasetuspto-grants-1990_11
ORD IDord-fc2363bad67f4ed6b0c0cc69f51c843c
Source noteuspto-grants-1990_11