Reaktion #1978177

ord-7ae01d16e73b4d3dbbb549bc0811dd19

Reaktionsgleichung

Nc1cccc(CS(N)(=O)=O)c1
(3-amino-phenyl)-methanesulfonamide
COc1ccccc1-c1cc(Cl)nc(N)n1
4-chloro-6-(2-methoxyphenyl)-pyrimidin-2-ylamine
COc1ccccc1-c1cc(Nc2cccc(CS(N)(=O)=O)c2)nc(N)n1
{3-[2-amino-6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-methanesulfonamide

Lösungsmittel

Reaktionsbedingungen

Temperatur
85°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevaporated in vacuo
  2. 2
    SonstigeThe resulting residue was purified by column chromatography on silica gel

Vorschrift

A mixture of (3-amino-phenyl)-methanesulfonamide (0.16 g, 0.85 mmol) and 4-chloro-6-(2-methoxyphenyl)-pyrimidin-2-ylamine (0.2 g, 0.85 mmol) in DMF (5 mL) was stirred at 80-90° C. till the reaction completion (TLC control), then evaporated in vacuo. The resulting residue was purified by column chromatography on silica gel yielding {3-[2-amino-6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-methanesulfonamide

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08507498B2uspto-grants-2013_08