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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350827Generated: October 31, 2026

1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride → 3-Chloro-4-(trifluoromethyl)phenoxyl-N-{3-methyl-4-[(methylsulfonyl)amino]benzyl}acetamide

https://huagongshe.com/reaction/1350827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chlorideHCID 10986715—
Reactant[3-Chloro-4-(trifluoromethyl)phenoxy]acetic acidHCID 21097484—
ReactantN-[4-(aminomethyl)-2-methylphenyl]methanesulfonamide hydrochlorideHCID 21097529—
SolventTriethylamineHCID 8471—
Product3-Chloro-4-(trifluoromethyl)phenoxyl-N-{3-methyl-4-[(methylsulfonyl)amino]benzyl}acetamideHCID 1166959267%

Reaction Steps

[3-Chloro-4-(trifluoromethyl)phenoxy]acetic acid (127 mg, 0.5 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (97 mg, 0.6 mmol), triethylamine (0.33 ml) and N{4-(aminomethyl)-2-methylphenyl]methanesulfonamide hydrochloride (151 mg, 0.6 mmol) were treated in the same procedure described in Example 2(b). The crude residue was applied to a silica gel chromatography column and eluted with a volume mixture of hexane and ethyl acetate (3/1 to 1/1) to furnish 150 mg (67% yield) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214824B2
Source datasetuspto-grants-2007_05
ORD IDord-37b36ae4724240e8a28d897160a28d48
Source noteuspto-grants-2007_05