Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372089Generated: November 1, 2026

Triethylamine → 4-Quinolone-3-carboxylic acid

https://huagongshe.com/reaction/2372089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 1508834HCID 1508834—
ReactantEthyl-pyrrolidin-3-ylmethyl-amineHCID 13491786—
SolventAcetonitrileHCID 6342—
Product4-Quinolone-3-carboxylic acidHCID 220875—

Reaction Steps

A suspension of 3.02 g (10 mmole) of 1-ethyl-5-amino-6,7,8-trifluoro-4-oxo-1,4-dihydro quinoline-3-carboxylic acid, 1.93 g (15 mmole) of N-ethyl-3-pyrrolidinemethanamine, 3.0 g (30 mmole) of triethylamine and 100 ml of acetonitrile is refluxed for 18 hours. The reaction mixture is cooled to room temperature and the precipitate is removed by filtration, washed with acetonitrile, ether, and dried in vacuo to give 1-ethyl-5-amino-6,8-difluoro-7-[3-(ethylamino)methyl-1-pyrrolidinyl)]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05097032
Source datasetuspto-grants-1992_03
ORD IDord-101435aaf05047029df4559fd8340b90
Source noteuspto-grants-1992_03