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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726304Generated: October 25, 2026

Triethylamine → 8-[2,6-dichloro-3-[N-methyl-N-((E)-styrylsulfonylglycyl)amino]benzyloxy]-2-methylquinoline

https://huagongshe.com/reaction/726304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(E)-2-phenylethene-1-sulfonyl chlorideHCID 5369377—
Reactant8-[3-(N-glycyl-N-methylamino)2,6-dichlorobenzyloxy]-2-methylquinolineHCID 11795484—
SolventDichloromethaneHCID 6344—
Product8-[2,6-dichloro-3-[N-methyl-N-((E)-styrylsulfonylglycyl)amino]benzyloxy]-2-methylquinolineHCID 2211314168.2%

Reaction Steps

To a solution of 8-[3-(N-glycyl-N-methylamino)-2,6-dichlorobenzyloxy]-2-methylquinoline (81 mg) and triethylamine (0.04 ml) in dichloromethane (2 ml) was added a solution of (E)-styrenesulfonyl chloride (48 mg) in dichloromethane (1 ml) in an ice-water bath. After being stirred for 30 minutes under ice-cooling, the reaction mixture was partitioned into dichloromethane and water. The organic layer was dried over magnesium sulfate and evaporated in vacuo. The residue was purified by preparative thin-layer chromatography (dichloromethane-methanol) to give 8-[2,6-dichloro-3-[N-methyl-N-((E)-styrylsulfonylglycyl)amino]benzyloxy]-2-methylquinoline (78 mg) as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708173
Source datasetuspto-grants-1998_01
ORD IDord-e8684d22257f4a4387f6429b732f93a2
Source noteuspto-grants-1998_01