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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344899Generated: October 30, 2026

Acetic Acid → (RS)-8-(3-benzyl-1-piperazinyl)-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/344899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(RS)-8-(3-benzyl-1-piperazinyl)-3-ethoxycarbonyl-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridineHCID 54492054—
SolventEthanolHCID 702—
SolventPotassium HydroxideHCID 14797—
Product(RS)-8-(3-benzyl-1-piperazinyl)-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 5367325982.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of (RS)-8-(3-benzyl-1-piperazinyl)-3-ethoxycarbonyl-7-fluoro-1-methyl-4-oxo-1,4dihydrobenzo[b][1,8]naphthyridine (2.65 g) in N aqueous potassium hydroxide (14 cc) and ethanol (20 cc) is heated to a temperature in the region of 80° C. for 20 minutes, treated at the same temperature with 5% strength acetic acid (32 cc) and stirred for 20 minutes. The insoluble matter is drained at approximately 80° C. and washed with water (2×20 cc), ethanol (2×20 cc) and ethyl ether (2×20 cc). After 2 recrystallizations in dimethylformamide (50 cc each time), (RS)-8-(3-benzyl-1-piperazinyl)-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (2.05 g) is obtained in the form of a yellow solid, decomposing at 270°-275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053509
Source datasetuspto-grants-1991_10
ORD IDord-040e5a16ce0e41309ed764b8d0845989
Source noteuspto-grants-1991_10