Reaktion #356660

ord-5ed0173ba89f407a903578dedc6ec0a3

Reaktionsgleichung

c1cnc2[nH]ccc2c1
7-azaindole
[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
O=C(Cl)Cc1cccc(F)c1F
(2,3-difluorophenyl)-acetyl chloride
O=C(Cc1cccc(F)c1F)c1c[nH]c2ncccc12
title compound
Ausbeute 13.0%
O=C(Cc1cccc(F)c1F)c1c[nH]c2ncccc12
2-(2,3-Difluoro-phenyl)-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)-ethanone
Ausbeute 13.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with methlene chloride
  2. 2
    Trocknendried (Na2SO4)
  3. 3
    Einengenconcentrated

Vorschrift

To 7-azaindole (1 g, 8.5 mmol) and AlCl3 (1.2 g, 9.0 mmol) in methlene chloride at 0° C. was added (2,3-difluorophenyl)-acetyl chloride [prepared by treating (2,3-difluoro-phenyl)-acetic acid (1.5 mg, 8.72 mmol) with oxalyl chloride (0.90 mL)] in methlene chloride. After stirring at room temperature for 2 hours, the solution was poured into ice water and extracted with methlene chloride, dried (Na2SO4), and concentrated to give 300 mg (13% yield) of title compound used without purification. LCMS Rt=3.00 minutes, MH+ 273.1, M− 271.1.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07446199B2uspto-grants-2008_11