HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | (1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amine | HCID 136335844 | — |
| Edukt | HCID 178506173 | HCID 178506173 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | [(1H-benzimidazol-2-yl)(3-trifluoromethylphenyl)methyl](1-methylpiperidin-4-yl)amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09029357B2 |
| Quelldatensatz | uspto-grants-2015_05 |
| ORD ID | ord-1307a4a9dfd7453aaf605f302d87ff9d |
| Quellennotiz | uspto-grants-2015_05 |