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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344906Generated: October 29, 2026

HCID 54470582, compound → (RS)-1-cyclopropyl-7-fluoro-8-[3-(4-methoxyphenyl)-1-piperazinyl]-4-oxo-1,4-dihydrobenzo [b][1,8]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/344906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54470582HCID 54470582—
SolventEthanolHCID 702—
SolventPotassium HydroxideHCID 14797—
Product(RS)-1-cyclopropyl-7-fluoro-8-[3-(4-methoxyphenyl)-1-piperazinyl]-4-oxo-1,4-dihydrobenzo [b][1,8]naphthyridine-3-carboxylic acidHCID 53972680105.7%

Reaction Steps

(RS)-1-Cyclopropyl-7-fluoro-8-[3-(4-methoxyphenyl)-1-piperazinyl]-4-oxo-1,4-dihydrobenzo [b][1,8]naphthyridine-3-carboxylic acid was prepared under the conditions of Example 29, but starting with (RS)-1-cyclopropyl-3-ethoxycarbonyl-7-fluoro-8-[3-(4-methoxyphenyl)-1-piperazinyl]-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine (1.5 g) in N aqueous potassium hydroxide (18.4 cc) and ethanol (18.4 cc). After 1 recrystallization in dimethylformamide (50 cc), (RS)-1-cyclopropyl-7-fluoro-8-[3-(4-methoxyphenyl)-1-piperazinyl]-4-oxo-1,4-dihydrobenzo [b][1,8]naphthyridine-3-carboxylic acid (1.5 g) is obtained in the form of a yellow solid, decomposing at 287° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053509
Source datasetuspto-grants-1991_10
ORD IDord-f02b6b31cd3943e89f351c9b03061b39
Source noteuspto-grants-1991_10