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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 572828Erstellt: 25. Oktober 2026

Water → [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine

https://huagongshe.com/reaction/572828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt(1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amineHCID 136335844—
EduktHCID 178506173HCID 178506173—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amineHCID 66835968—

Reaktionsschritte

To a solution of (1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amine (70 mg) in tetrahydrofurane (3 mL) is added a 1.5M solution of 3-trifluoromethylphenylmagnesium bromide in tetrahydrofurane (0.77 mL) at room temperature. The mixture is then stirred at 40° C. for 1 h, hydrolyzed with water and extracted with ethyl acetate. The pooled organic extracts are washed with brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by column chromatography (gradient dichloromethane/methanol/ammonia from 95/5/0.5 to 90/10/0.5) to give [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine as a yellow solid melting at 90° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09029357B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-1307a4a9dfd7453aaf605f302d87ff9d
Quellennotizuspto-grants-2015_05