Reaktion #356665

ord-97b5414125a94f1fa05a61292c482fa6

Reaktionsgleichung

O=C(Cl)Cc1cccc(F)c1F
(2,3-Difluoro-phenyl)-acetyl chloride
CN(C)CC#Cc1cnc2[nH]ccc2c1
Dimethyl-[3-(1H-pyrrolo[2,3-b]pyridin-5-yl)-prop-2-ynyl]-amine
[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
CN(C)CC#Cc1cnc2[nH]cc(C(=O)Cc3cccc(F)c3F)c2c1
2-(2,3-Difluoro-phenyl)-1-[5-(3-dimethylamino-prop-1-ynyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-ethanone

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe reaction

Vorschrift

189 mg of crude Dimethyl-[3-(1H-pyrrolo[2,3-b]pyridin-5-yl)-prop-2-ynyl]-amine was stirred in 5 ml of DCM with AlCl3 (4 equivalents) for 30 minutes. Two equivalents of (2,3-Difluoro-phenyl)-acetyl chloride were added and the reaction was stirred in a sealed tube overnight. The LC/MS showed the reaction to be complete and was worked-up under standard conditions. Normal phase column chromatography yielded 101 mg of 2-(2,3-Difluoro-phenyl)-1-[5-(3-dimethylamino-prop-1-ynyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-ethanone with a yield over two steps of 33%. LC/MS retention time of 1.83 minutes. M+ 354.17, M− 352.1

Quelle

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