Reaktion #88412

ord-f2c2b502275b4457a2d77a9bb4faf6f8

Reaktionsbedingungen

Temperatur
3°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe precipitated solid was collected by filtration
  2. 2
    Waschenwas then washed with water (45 ml)
  3. 3
    Sonstigeto obtain a white solid as a crude product
  4. 4
    Temperaturthe obtained mixture was then cooled to 3° C
  5. 5
    SonstigeThe obtained crude product
  6. 6
    workup.STIRRINGThe obtained mixture was stirred at 3° C. for 30 minutes
  7. 7
    Filtrationthe precipitated solid was collected by filtration
  8. 8
    WaschenThe collected solid was washed with methyl tert-butyl ether (20 ml)
  9. 9
    Sonstigewas then dried at 45° C.

Vorschrift

70% Perchloric acid (18.9 ml) was added to a 1,4-dioxane (26 ml) solution of (Z)-ethyl N-(mesitylsulfonyl)oxyacetimidate (11.7 g) at 4° C. over 20 minutes. Thereafter, the reaction solution was stirred at 3° C. for 30 minutes, and it was then poured into water (100 ml). The precipitated solid was collected by filtration, and was then washed with water (45 ml) to obtain a white solid as a crude product. Methyl 2-aminoisonicotinate (5 g) was added to methylene chloride (35 ml), and the obtained mixture was then cooled to 3° C. The obtained crude product was dissolved in methylene chloride (40 ml), and only an organic layer was added to a methylene chloride solution of 2-aminoisonicotinate. The obtained mixture was stirred at 3° C. for 30 minutes. Thereafter, methyl tert-butyl ether (50 ml) was added to the reaction solution, and the precipitated solid was collected by filtration. The collected solid was washed with methyl tert-butyl ether (20 ml), and was then dried at 45° C., so as to obtain the title compound (10.7 g) in the form of a light yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440970B2uspto-grants-2016_09