HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244465Erstellt: 24. Oktober 2026
1-Methyl-3-(trifluoroacetyl)-1H-indole → HCID 59437212, Verbindung
https://huagongshe.com/de/reaction/244465
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Methyl-3-(trifluoroacetyl)-1H-indole | HCID 3524388 | — |
| Edukt | 5-Bromo-1-(4-fluorophenyl)-3-methyl-1,3-dihydro-benzimidazol-2-one | HCID 59437286 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 59437212 | HCID 59437212 | 12,8% |
Reaktionsschritte
To a chilled (−78° C.) solution of 5-bromo-1-(4-fluorophenyl)-3-methyl-1,3-dihydro-benzimidazol-2-one (80 mg, 0.25 mmol) in anhydrous THF (3 mL) was added tert-butyllithium (0.2 mL of 1.7 M solution in heptane, 0.34 mmol). After 1 minute, a chilled (−78° C.) solution of 2,2,2-trifluoro-1-(1-methyl-1H-indol-3-yl)ethanone (57 mg, 0.25 mmol) in anhydrous THF (1 mL) was added. After 10 minutes, the mixture was quenched with ammonium chloride solution and extracted with three 15 mL portions of methylene chloride. The combined organic layers were washed with water, dried over anhydrous sodium sulfate, and concentrated in vacuo to afford a brownish oil. The residue was purified by column chromatography over silica gel eluting with 0-10% ethyl acetate in methylene chloride to afford 15 mg of the title compound as a white powder. MS m/z 470 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08658637B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-b80428248671469ab8751842b05dafcb |
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| Quellennotiz | uspto-grants-2014_02 |
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