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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620887Generated: October 29, 2026

Triethylamine → 4-Quinolone-3-carboxylic acid

https://huagongshe.com/reaction/620887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 1508834HCID 1508834—
Reactanttert-butyl N-(pyrrolidin-3-yl)carbamateHCID 2757234—
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, 2.79 g (15 mmole) of 3-(t-butoxycarbonylamino)pyrrolidine, 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-(t-butoxycarbonylamino)-1-pyrrolidinyl[-4-oxo-1,4-dihydroquinoline-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822801
Source datasetuspto-grants-1989_04
ORD IDord-fc3b050b6acf4b52a8e3888a127e5835
Source noteuspto-grants-1989_04