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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290522Generated: October 31, 2026

6,7,8-Trifluoro-1,4-dihydro-4-oxo-1-(2-thiazolyl)-3-quinolinecarboxylic acid → 7-[3[(Ethylamino)methyl]-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-1-(2-thiazolyl)-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/2290522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6,7,8-Trifluoro-1,4-dihydro-4-oxo-1-(2-thiazolyl)-3-quinolinecarboxylic acidHCID 11823570—
ReactantEthyl-pyrrolidin-3-ylmethyl-amineHCID 13491786—
SolventAcetonitrileHCID 6342—
Product7-[3[(Ethylamino)methyl]-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-1-(2-thiazolyl)-3-quinolinecarboxylic acidHCID 1372833224.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 1.0 g (3.06 mmol) of the 6,7,8-trifluoro-1,4-dihydro-4-oxo-1-(2-thiazolyl)-3-quinolinecarboxylic acid in 10 ml of acetonitrile was added 0.46 g of 1,8-diazobicyclo[5.4.0]undec-7-ene and 0.39 g of 3-[(ethylamino)methyl]pyrrolidine. The reaction was warmed to 60° C. for one hour and was then taken to room temperature and stirred overnight. The solids were filtered and washed with ether to give 0.32 g of 7-[3[(ethylamino)methyl]-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-1-(2-thiazolyl)-3-quinolinecarboxylic acid, mp 200°-207° (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04617308
Source datasetuspto-grants-1986_10
ORD IDord-0497da5386684e708b28b149aca592c9
Source noteuspto-grants-1986_10