Reaktion #1006907

ord-29eef97f659f4d18861c1db73301e22d

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was evaporated in vacuo
  2. 2
    Sonstigethe residue was purified by silica gel chromatography (5-60% EtOAc/hexanes+2% AcOH)

Vorschrift

A mixture of 7-benzyl-4-hydroxy-8-oxo-7,8-dihydro-[2,7]naphthyridine-3-carboxylic acid methyl ester (40 mg, 0.13 mmol) and ammonia (10 mL, 7 M in MeOH) was stirred at r.t. for 16 h. The solvent was evaporated in vacuo, and the residue was purified by silica gel chromatography (5-60% EtOAc/hexanes+2% AcOH) to give 18 mg of the title compound as a light yellow solid. MS: (+) m/z 296.06 (M+1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09271970B2uspto-grants-2016_03