Reaktion #47871

ord-8f8c352671c94590927e6ea4b4fc753b

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was evaporated to dryness in vacuo
  2. 2
    SonstigeThe residue was chromatographed on silica gel
  3. 3
    Wascheneluted with the following solvent system

Vorschrift

5,7-Dichloro-3-isopropylpyrazolo[4,3-d]pyrimidine (90 mg), 1.2 mL of 3-chloroaniline and 250 μL of diisopropyl ethylamine were stirred at 60° C. for 24 hours. The reaction mixture was evaporated to dryness in vacuo. The residue was chromatographed on silica gel eluted with the following solvent system: CHCl3/heptane (100/17), to give 7-(3-chloroanilino)-5-chloro-3-isopropylpyrazolo[4,3-d]pyrimidine, yield 16%, mp=257-259° C. MS (ES+): 322.3 (100%, M+H+), 324.3 (64%, M+H+). 1H NMR (CDCl3; 300 MHz): 1.54 d (6H, J=7.1 Hz); 3.60 sept (1H, J=7.1 Hz), 7.16 d (1H), 7.34 t (1H), 7.88 d (1H), 8.10 s (1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745450B2uspto-grants-2010_06