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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344855Generated: October 25, 2026

2-(4-Fluorophenyl)piperazine → (RS)-1-Ethyl-7-fluoro-4-oxo-8-[3-(4-fluorophenyl)-1-piperazinyl]-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/344855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Fluorophenyl)piperazineHCID 4617623—
Reactant8-Chloro-1-ethyl-7-fluoro-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700555—
SolventPyridineHCID 1049—
Product(RS)-1-Ethyl-7-fluoro-4-oxo-8-[3-(4-fluorophenyl)-1-piperazinyl]-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 5382405042.3%

Reaction Steps

The reaction is performed under the conditions of Example 4, but starting with 8-chloro-1-ethyl-7-fluoro-4-oxo-1,4-dihydrobenzo[b][1,8 ]-naphthyridine-3-carboxylic acid (1.5 g) and (RS)-2-(4-fluorophenyl)piperazine (3.4 g) in pyridine (15 cc). (RS)-1-Ethyl-7-fluoro-4-oxo-8-[3-(4-fluorophenyl)-1-piperazinyl]-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (0.92 g) is obtained in the form of a yellow solid, m.p. 298° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053509
Source datasetuspto-grants-1991_10
ORD IDord-c58e21139aa048aead8f63054985faa1
Source noteuspto-grants-1991_10