Reaktion #1379889

ord-02e64fcc1c34429789c49e94ff5532f7

Reaktionsgleichung

[Na+].[OH-]
sodium hydroxide
COC(=O)c1ccc(Nc2cccc3ncccc23)cc1
product
COC(=O)c1ccc(Nc2cccc3ncccc23)cc1
4-(quinolin-5-ylamino)-benzoic Acid Methyl Ester
O=C(O)c1ccc(Nc2cccc3ncccc23)cc1
orange powder
O=C(O)c1ccc(Nc2cccc3ncccc23)cc1
4-(quinolin-5-ylamino)-benzoic Acid

Reaktionsbedingungen

Temperatur
50°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas removed under reduced pressure
  2. 2
    SonstigeThe resultant residue was purified
  3. 3
    workup.DISSOLUTIONby dissolving in water (1000 ml)
  4. 4
    Sonstigeprecipitating the crude product by acidification to pH3 with 2N HCl
  5. 5
    SonstigeThe precipitate so formed
  6. 6
    Filtrationwas collected by filtration
  7. 7
    Waschenwashed with water (250 ml)
  8. 8
    SonstigeThis purification procedure
  9. 9
    Sonstigewas dried

Vorschrift

A solution of sodium hydroxide (7 g, 0.18 mol) in water (100 ml) was added to a solution of the product from stage (a) in a mixture of tetrahydrofuran (100 ml) and methanol (350 ml). The reaction mixture was stirred at 50° C. for 3 h before the solvent was removed under reduced pressure. The resultant residue was purified by dissolving in water (1000 ml) adjusted to pH10 with 2M NaOH and precipitating the crude product by acidification to pH3 with 2N HCl. The precipitate so formed was collected by filtration and washed with water (250 ml). This purification procedure was repeated a further two times before the product was dried to give 12.3 g of an orange powder.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07238228B2uspto-grants-2007_07