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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619117Generated: October 26, 2026

Sodium Bicarbonate → 6-fluoro-1-methyl-4-[2-[4-(thieno[3,2-c]pyridine-4-yl)-1-piperazinyl]ethyl]-2(1H)-quinolone hydrochloride

https://huagongshe.com/reaction/619117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Piperazin-1-yl)thieno[3,2-c]pyridineHCID 10966027—
Reactant4-(2-chloroethyl)-6-fluoro-1-methyl-2(1H)-quinoloneHCID 21846043—
SolventAcetonitrileHCID 6342—
Product6-fluoro-1-methyl-4-[2-[4-(thieno[3,2-c]pyridine-4-yl)-1-piperazinyl]ethyl]-2(1H)-quinolone hydrochlorideHCID 2184603927%

Reaction Conditions

Temperature57.5 °C

Reaction Steps

1.4 g (5.8 mmol) of 4-(2-chloroethyl)-6-fluoro-1-methyl-2(1H)-quinolone are added to a mixture of 1.3 g (5.9 mmol) of 4-(1-piperazinyl)thieno[3,2-c]pyridine and 0.50 g (5.95 mmol) of sodium hydrogen carbonate in 20 ml of acetonitrile, and the reaction medium is heated to 55-60° C. for 18 hours. The solvent is evaporated off and the residue is taken up in 100 ml of dichloromethane. It is washed with saturated aqueous sodium bicarbonate solution and then with water. The organic phase is dried over sodium sulphate and filtered and the filtrate is condensed. The crude product is purified by flash chromatography on silica, eluting with a methanol/dichloromethane (5:95) mixture containing traces of aqueous ammonia. 0.70 g of the expected product is obtained in base form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05958924
Source datasetuspto-grants-1999_09
ORD IDord-0176029c30724412b685e2b0d7b42484
Source noteuspto-grants-1999_09