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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828557Generated: November 1, 2026

Dimethyl Sulfide → HCID 22063563, compound

https://huagongshe.com/reaction/1828557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 22063507HCID 22063507—
Solvent1,2-DichloroethaneHCID 11—
SolventChloroformHCID 6212—
ProductHCID 22063563HCID 220635633%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of aluminum chloride (266 mg, 2.00 mmol) in 1,2-dichloroethane (4 ml) was added with dimethyl sulfide (0.293 ml, 4.00 mmol) and stirred at 0° C. for 30 minutes. Then, the reaction mixture was added with ethyl 1-cyclopropyl-6-fluoro-7-[(4-isopropyl-1,3-thiazol-2-yl)methyl]-2-morpholino-4-oxo-1,4-dihydro-3-quinolinecar boxylate (51.5 mg, 0.0999 mmol) and refluxed overnight by heating. The reaction mixture was left stand for cooling, diluted with chloroform, washed with 1 N hydrochloric acid, and dried over anhydrous magnesium sulfate. The solvent was evaporated and the obtained residue was purified by preparative TLC (chloroform:methanol=10:1) to obtain the title compound (1.3 mg, 3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056917B2
Source datasetuspto-grants-2006_06
ORD IDord-35736636a3f54a32ba9ad54cded121b3
Source noteuspto-grants-2006_06