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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2273331Erstellt: 26. Oktober 2026

Citric Acid → 3-Ethylsulfanyl pyridin-2-carboxylic acid [2-(2,2,2-trifluoroethyl)amino-5-trifluoromethylpyridin-3-yl]amide

https://huagongshe.com/reaction/2273331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt3-(Ethylsulfanyl)pyridine-2-carboxylic acidHCID 79006954—
EduktN2-(2,2,2-trifluoroethyl)-5-trifluoromethylpyridine-2,3-diamineHCID 86725179—
LösungsmittelPyridineHCID 1049—
Produkt3-Ethylsulfanyl pyridin-2-carboxylic acid [2-(2,2,2-trifluoroethyl)amino-5-trifluoromethylpyridin-3-yl]amideHCID 9032421288,1%

Reaktionsschritte

A mixture of N2-(2,2,2-trifluoroethyl)-5-trifluoromethylpyridin-2,3-diamine (0.52 g), 3-ethylsulfanylpyridin-2-carboxylic acid (0.37 g), WSC (0.46 g), HOBt (27 mg) and pyridine (2 ml) was stirred at room temperature for 3 hours. To the reaction mixture was poured aqueous 10% citric acid solution, and then the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over sodium sulfate, and concentrated under reduced pressure to give 3-ethylsulfanyl pyridin-2-carboxylic acid [2-(2,2,2-trifluoroethyl)amino-5-trifluoromethylpyridin-3-yl]amide (0.75 g), which is hereinafter referred to as “intermediate compound (M3-43)”.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09120823B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-1225677c803d42a09aad29db42533660
Quellennotizuspto-grants-2015_09