Reaktion #1536745

ord-6f566a4e791f43e39446d5d25129b9c0

Reaktionsgleichung

COC(=O)c1c(N)cccc1OC
methyl 2-amino-6-methoxybenzoate
COC(=O)C#CC(=O)OC
dimethyl acetylenedicarboxylate
CC(C)(C)[O-].[K+]
potassium t-butoxide
COC(=O)c1nc2cccc(OC)c2c(O)c1C(=O)OC
desired compound
Ausbeute 65.0%
COC(=O)c1nc2cccc(OC)c2c(O)c1C(=O)OC
Dimethyl 4-hydroxy-5-methoxyquinoline-2,3-dicarboxylate
Ausbeute 65.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    Sonstigeprecipitated out of solution
  3. 3
    TemperaturThe mixture was cooled to room temperature
  4. 4
    Filtrationfiltered
  5. 5
    workup.DISSOLUTIONthe collected solids were dissolved in water
  6. 6
    Sonstigeto form a light tan precipitate
  7. 7
    SonstigeThe solids were collected
  8. 8
    Filtrationfiltered
  9. 9
    Waschenwashed with water and air
  10. 10
    Sonstigedried

Vorschrift

A solution of methyl 2-amino-6-methoxybenzoate ((1.30 g, 7.17 mM) and dimethyl acetylenedicarboxylate (1.17 g, 8.23 mM) in t-butanol (11 mL) was refluxed under a nitrogen atmosphere for 4 hr. The reaction mixture was cooled to-room temperature, potassium t-butoxide (0.92 g, 8.23 mM) was added, and the resulting mixture was heated to 90° C. for 1.5 hr during which solids precipitated out of solution. The mixture was cooled to room temperature, filtered and the collected solids were dissolved in water. The resulting solution was acidified with 1N H2SO4 to form a light tan precipitate. The solids were collected, filtered, washed with water and air dried to provide the desired compound (1.35 g, 65%) as a tan solid. A 0.28 g portion of this material was recrystallized from ethyl acetate to provide an analytical sample (0.24 g) of the title compound as a white solid, mp 184°-186° C.; MS(CI): 292 (M+H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05599814uspto-grants-1997_02