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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198573Generated: October 26, 2026

7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid → 1-Ethyl-6-fluoro-7-[3-[(isopropylamino)methyl]pyrrolidin-1-yl]-4-oxo-1,8-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/1198573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 12790859—
ReactantN-(Pyrrolidin-3-ylmethyl)propan-2-amineHCID 13491802—
SolventAcetonitrileHCID 6342—
Product1-Ethyl-6-fluoro-7-[3-[(isopropylamino)methyl]pyrrolidin-1-yl]-4-oxo-1,8-naphthyridine-3-carboxylic acidHCID 46140917.7%

Reaction Steps

A near solution of 0.82 g (3.0 mmole) of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8 -naphthyridine-3-carboxylic acid and 1.4 g (10 mmole) of N-(2-propyl)-3-pyrrolidinemethanamine in 50 mL of acetonitrile was heated at reflux for one hour. The solvent was removed in vacuo, the residue dissolved in water, filtered through a fiber glass pad to clarify and the filtrate adjusted to pH 2.0 with 6M hydrochloric acid. The resulting clear solution was lyophilized and the residue recrystallized from ethanol to give 200 mg of 1-ethyl-6-fluoro-1,4-dihydro-7-[3-[[(1 -methylethyl)amino]methyl]-1-pyrrolidinyl]-4-oxo-l,8-naphthyridine-3-carboxylic acid, mp 302°-304° C. as the hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281612
Source datasetuspto-grants-1994_01
ORD IDord-b177a24793144524b7d969c6c0f9730b
Source noteuspto-grants-1994_01