Reaktion #1606171

ord-9427481d1a0648acbd7a2c8f642037ce

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture was concentrated in vacuo
  2. 2
    Sonstigethe residue partitioned between dichloromethane (3 ml) and water (3 ml)
  3. 3
    SonstigeThe organic layer was separated
  4. 4
    Sonstigedried by passage through a hydrophobic frit
  5. 5
    Einengenconcentrated in vacuo
  6. 6
    SonstigeThe crude residue was purified by preparative HPLC

Vorschrift

A solution of 3-[(4-chloro-benzyl)-(1-methyl-1H-pyrazole-3-sulfonyl)-amino]-benzoic acid (30 mg, 0.07 mmol), diisopropylethylamine (0.26 ml, 0.14 mmol), HATU (56 mg, 0.15 mmol) and 2-aminoethanol (9 μL, 0.14 mmol) were stirred in dry acetonitrile (3 ml) for 18 hrs. The reaction mixture was concentrated in vacuo and the residue partitioned between dichloromethane (3 ml) and water (3 ml). The organic layer was separated and dried by passage through a hydrophobic frit, then concentrated in vacuo. The crude residue was purified by preparative HPLC to afford the title compound as an off white solid (11.9 mg). HPLC retention time 5.03 min. Mass spectrum (ES+) m/z 449 (M+H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09073834B2uspto-grants-2015_07