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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 533647Erstellt: 25. Oktober 2026

1-Hydroxybenzotriazole → 2-(2-ethylsulfanyl-phenyl)-3-methyl-6-trifluoromethyl-3H-benzimidazole-4-ylamine

https://huagongshe.com/reaction/533647

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt2-(Ethylsulfanyl)benzoic acidHCID 425758—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktN'-methyl-5-trifluoromethyl-benzene-1,2,3-triamineHCID 68091212—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
Produkt2-(2-ethylsulfanyl-phenyl)-3-methyl-6-trifluoromethyl-3H-benzimidazole-4-ylamineHCID 6798168715,2%

Reaktionsschritte

To a mixture of N′-methyl-5-trifluoromethyl-benzene-1,2,3-triamine (1.3 g), 2-ethylsulfanylbenzoic acid (1.3 g), and pyridine (12 mL), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.4 g) and 1-hydroxybenzotriazole (86 mg) were added at room temperature. The mixture was stirred at room temperature for 5 hours, then heated to 110° C., and stirred with heating for 8 hours. After the reaction mixture was allowed to cool to room temperature, the reaction mixture was diluted with water, and extracted with ethyl acetate. The combined organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 339 mg of 2-(2-ethylsulfanyl-phenyl)-3-methyl-6-trifluoromethyl-3H-benzimidazole-4-ylamine (hereinafter, Present Compound 336).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08853238B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-0cbd1663b2d84c7797cd713e2e24c962
Quellennotizuspto-grants-2014_10