Reaktion #3300

ord-68d8ae5623a045faa4752c54188d8074

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux for 10 minutes
  2. 2
    SonstigeCrystals separated on inducement
  3. 3
    workup.ADDITIONAn additional 3 drops of water were added
  4. 4
    Sonstigeto precipitate additional tacky solid
  5. 5
    SonstigeAfter decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether
  6. 6
    FiltrationThe solids were filtered
  7. 7
    Waschenwashed with 50% ethyl acetate/petroleum ether
  8. 8
    Sonstigedried
  9. 9
    SonstigePurification
  10. 10
    Filtrationby filtering an ethyl acetate solution through a layer of silica gel
  11. 11
    SonstigeConcentration of the filtrate to 1 mL volume yielded pure crystalline product

Vorschrift

A solution of 0.100 g (0.25 mmol) of 6-(2,6-dichlorophenyl)-8-ethyl-2-methanesulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 68 and 0.061 g (0.50 mmol) of 4-methoxyaniline in 0.5 mL of dimethylformamide was heated at reflux for 10 minutes. Three drops of water were added. Crystals separated on inducement. An additional 3 drops of water were added to precipitate additional tacky solid. After decantation, the solid was triturated with 0.5 mL of ethyl acetate and 0.5 mL of petroleum ether. The solids were filtered and washed with 50% ethyl acetate/petroleum ether and dried; wt 0.080 g. Purification was effected by filtering an ethyl acetate solution through a layer of silica gel. Concentration of the filtrate to 1 mL volume yielded pure crystalline product; wt 0.033 g; mp 213°-215° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733914uspto-grants-1998_03