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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428788Generated: November 3, 2026

(2-m-Tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamine → HCID 89455636, compound

https://huagongshe.com/reaction/1428788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-m-Tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamineHCID 86680208—
ReactantHCID 131732364HCID 131732364—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductHCID 89455636HCID 8945563651%

Reaction Conditions

Temperature50 °C

Reaction Steps

2-(N-(2-Fluoro-4-(phenoxycarbonylamino)benzyl)sulfamoylcarbamoyloxy)-2-methylpropan-1-ylium (100 mg, 0.225 mmol) was dissolved in acetonitrile. (2-m-Tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamine (60 mg, 0.225 mmol) and 4-dimethylaminopyridine (27 mg) were added to the solution. The reaction mixture was stirred for overnight at 50° C. The mixture was extracted with ethyl acetate and washed with brine. Drying over magnesium sulfate, evaporation of the ethyl acetate and purification by column chromatography gave tert-butyl N-(2-fluoro-4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)sulfamoylcarbamate (70 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-4a930dd291f7404a9a9cf9f2722421a6
Source noteuspto-grants-2015_01