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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994000Generated: November 1, 2026

Dimethylformamide → 4-[3-(3-Trifluoromethyl-benzenesulfonylamino)-benzo[1,2,4]triazin-7-yloxy]-pyridine-2-carboxylic acid methyl amide trifluoroacetate salt

https://huagongshe.com/reaction/1994000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
Reactant4-((3-Aminobenzo[e][1,2,4]triazin-7-yl)oxy)-N-methylpicolinamideHCID 59135329—
ReactantHCID 178418922HCID 178418922—
Product4-[3-(3-Trifluoromethyl-benzenesulfonylamino)-benzo[1,2,4]triazin-7-yloxy]-pyridine-2-carboxylic acid methyl amide trifluoroacetate saltHCID 86604283—

Reaction Conditions

Temperature100 °C

Reaction Steps

100 mg (0.337 mmol, 1.0 equivalent) of 4-(3-amino-benzo[1,2,4]triazin-7-yloxy)-pyridine-carboxylic acid methylamide were dissolved in 2 mL of anhydrous dimethylformamide with heating to about 100° C. 45.4 mg (0.405 mmol, 1.2 equivalent) of solid tert-BuOK was added to the solution. The resulting dark-red solution was stirred at 100° C. for 30 min, then it was allowed to cool down to ambient temperature. 100 mg (0.405 mmol, 1.2 equivalent) of 3-trifluoromethyl-benzenesulfonyl chloride was added to the mixture via a syringe. It was allowed to stir at ambient temperature for 2 hours. The reaction mixture was filtered through 0.22 g syringe filter and purified by reverse-phase preperative HPLC using acetonitrile/water mixture with 0.1% of TFA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-1f08baf0619646918da074a665c7668f
Source noteuspto-grants-2010_01