Reaktion #1978194

ord-cc7ab4dcabe94485bb9b4fe45fe736a9

Reaktionsgleichung

Nc1cccc(CS(N)(=O)=O)c1
(3-amino-phenyl)-methanesulfonamide
COCCOc1ccccc1-c1cc(Cl)nc(C)n1
4-chloro-6-[2-(2-methoxy-ethoxy)-phenyl]-2-methyl-pyrimidine
COCCOc1ccccc1-c1cc(Nc2cccc(CS(N)(=O)=O)c2)nc(C)n1
(3-{6-[2-(2-methoxy-ethoxy)-phenyl]-2-methyl-pyrimidin-4-ylamino}-phenyl)-methanesulfonamide

Lösungsmittel

Reaktionsbedingungen

Temperatur
90°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 (0.1 g, 0.54 mmol) and 4-chloro-6-[2-(2-methoxy-ethoxy)-phenyl]-2-methyl-pyrimidine (0.16 g, 0.0.57 mmol) in DMF (3 mL) was stirred at 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-{6-[2-(2-methoxy-ethoxy)-phenyl]-2-methyl-pyrimidin-4-ylamino}-phenyl)-methanesulfonamide (Compound 83) as beige powder.

Quelle

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