Reaktion #333618

ord-acc7fcafef77470e94fe641360589037

Reaktionsgleichung

Cn1ccc2cccc(B3OC(C)(C)C(C)(C)O3)c21
Methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
CC(C)(C)NC(=O)c1cn(COCC[Si](C)(C)C)c2ncc(Br)nc12
2-Bromo-N-tert-butyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1cc2cccc(B3OC(C)(C)C(C)(C)O3)c2[nH]1
2-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Cc1cc2cccc(-c3cnc4c(n3)c(C(=O)NC(C)(C)C)cn4COCC[Si](C)(C)C)c2[nH]1
N-tert-butyl-2-(2-methyl-1H-indol-7-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide
Ausbeute 73.6%

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewater (0.5 mL), then the reaction was purged with nitrogen for 1 minute
  2. 2
    Temperaturthe reaction was heated at 80° C. for an additional 2 h
  3. 3
    TemperaturThe reaction mixture was cooled
  4. 4
    Waschenwashed water and brine
  5. 5
    Trocknendried (MgSO4)
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated in vacuo
  8. 8
    SonstigeThe crude residue was purified by chromatography (silica gel, 3-15% ethyl acetate in hexanes)

Vorschrift

2-Bromo-N-tert-butyl-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (79 mg, 185 μmol), potassium carbonate (51.1 mg, 370 μmol) and 2-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole (95.1 mg, 370 μmol) were dissolved in dioxane (5 mL) and water (0.5 mL), then the reaction was purged with nitrogen for 1 minute. Tetrakis(triphenylphosphine)palladium(0) (21.4 mg, 18.5 μmol) was then added, and the reaction was placed under a nitrogen atmosphere and the mixture heated at to 80° C. for 2 h. Methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole (45 mg), was added and the reaction was heated at 80° C. for an additional 2 h. The reaction mixture was cooled, diluted with ethyl acetate/ether (ca 3:1), washed water and brine, dried (MgSO4), filtered and concentrated in vacuo. The crude residue was purified by chromatography (silica gel, 3-15% ethyl acetate in hexanes) to give N-tert-butyl-2-(2-methyl-1H-indol-7-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (65 mg) as an oil. MS (M+H)+=478.3.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08658646B2uspto-grants-2014_02