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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085783Generated: November 1, 2026

tert-Butanol → 6,8-Difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid

https://huagongshe.com/reaction/1085783

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantPotassium HydroxideHCID 14797—
Reactantethyl 6,8-difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylateHCID 10000764—
SolventWaterHCID 962—
Product6,8-Difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acidHCID 1024838092.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 0.5 g of ethyl 6,8-difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate was added 10 ml of 5% solution of potassium hydroxide in a 3:1 mixture of tert-butanol and water and the mixture was stirred at 60° C. for 30 minutes. tert-Butanol was evaporated therefrom in vacuo and the residue was neutralized with acetic acid. After cooling, the crystals separated out therefrom were collected by filtration, washed with water and then washed with acetone and ether to give 0.43 g of the title product, m.p. 260° C. (decompn.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011831
Source datasetuspto-grants-1991_04
ORD IDord-3f8bc9ea90af4344b2e23845e1db3f16
Source noteuspto-grants-1991_04