Reaktion #1978191

ord-ecadf2fd796146ed823dbc01d51eb61c

Reaktionsgleichung

Nc1cccc(CS(N)(=O)=O)c1
(3-amino-phenyl)-methanesulfonamide
Clc1cc(-c2ccccc2OCC2CCCO2)ncn1
4-chloro-6-[2-(tetrahydro-furan-2-ylmethoxy)-phenyl]-pyrimidine
NS(=O)(=O)Cc1cccc(Nc2cc(-c3ccccc3OCC3CCCO3)ncn2)c1
(3-{6-[2-(tetrahydro-furan-2-ylmethoxy)-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 (0.18 g, 0.62 mmol) and 4-chloro-6-[2-(tetrahydro-furan-2-ylmethoxy)-phenyl]-pyrimidine (0.115 g, 0.62 mmol) in DMF (3 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-{6-[2-(tetrahydro-furan-2-ylmethoxy)-phenyl]-pyrimidin-4-ylamino}-phenyl)-methanesulfonamide (Compound 82) as white solid.

Quelle

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