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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Methyl-3-(trifluoroacetyl)-1H-indoleHCID 3524388—
Edukt5-Bromo-1-(4-fluorophenyl)-3-methyl-1,3-dihydro-benzimidazol-2-oneHCID 59437286—
EduktHCID 178418306HCID 178418306—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 59437212HCID 5943721212,8%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658637B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-b80428248671469ab8751842b05dafcb
Quellennotizuspto-grants-2014_02