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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 533620Erstellt: 26. Oktober 2026

Pyridine → 7-bromo-2-(2-ethylsulfanylphenyl)-1-methyl-5-trifluoromethyl-1H-benzimidazole

https://huagongshe.com/reaction/533620

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Edukt2-(Ethylsulfanyl)benzoic acidHCID 425758—
Edukt3-bromo-N2-methyl-5-trifluoromethylbenzene-1,2-diamineHCID 86061318—
LösungsmittelWaterHCID 962—
Produkt7-bromo-2-(2-ethylsulfanylphenyl)-1-methyl-5-trifluoromethyl-1H-benzimidazoleHCID 6798433843,2%

Reaktionsbedingungen

Temperatur115 °C

Reaktionsschritte

A mixture of 3-bromo-N2-methyl-5-trifluoromethylbenzene-1,2-diamine (2.22 g), 2-ethylsulfanylbenzoic acid (1.80 g), WSC (1.40 g), and pyridine (10 ml) was stirred under reflux at 115° C. for 6 hours. Into the reaction mixture cooled to room temperature, water was poured, and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to give 1.48 g of 7-bromo-2-(2-ethylsulfanylphenyl)-1-methyl-5-trifluoromethyl-1H-benzimidazole (hereinafter referred to as Present Compound 74).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08853238B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-e941f0879f0546ac9e7860b8073f78cb
Quellennotizuspto-grants-2014_10