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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052927Generated: October 26, 2026

1-Hydroxybenzotriazole → 2-ethylsulfanyl-4-trifluoromethyl-N-(5-trifluoromethyl-pyri din-2-yl)-benzamide

https://huagongshe.com/reaction/1052927

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(Ethylthio)-4-(trifluoromethyl)benzoic acidHCID 91876372—
SolventPyridineHCID 1049—
Product2-ethylsulfanyl-4-trifluoromethyl-N-(5-trifluoromethyl-pyri din-2-yl)-benzamideHCID 11803509765%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1.62 g of 2-amino-5-trifluoromethylpyridine, 2.5 g of 2-ethylsulfanyl-4-trifluoromethylbenzoic acid, 2.3 g of EDCI hydrochloride, 0.13 g of HOBt and 5 mL of pyridine was stirred at room temperature for 2 hours and at 60° C. for 1 hour. A saturated aqueous sodium bicarbonate solution was added to the cooled reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 2.56 g of 2-ethylsulfanyl-4-trifluoromethyl-N-(5-trifluoromethyl-pyridin-2-yl)-benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09392791B2
Source datasetuspto-grants-2016_07
ORD IDord-2cb9444d3b4547088d144d19f3398ee6
Source noteuspto-grants-2016_07