Reaktion #4536

ord-25cf147f10cf48b9989fcb580416b649

Reaktionsgleichung

COC(C)=O
methyl acetate
CC(=O)OCc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Ausbeute 54.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated to the boil
  2. 2
    workup.DISTILLATIONwas slowly distilled off in the course of 5 hours
  3. 3
    SonstigeThe mixture was then evaporated down to one-third of its total volume
  4. 4
    Sonstigethe precipitated crystals were isolated
  5. 5
    Sonstigerecrystallized from ethyl acetate

Vorschrift

A mixture of 15 g (0.04 mole) of 3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine, 150 ml of methanol and 0.15 g of p-toluenesulfonic acid was heated to the boil, and a mixture of methanol and methyl acetate was slowly distilled off in the course of 5 hours. The mixture was then evaporated down to one-third of its total volume, and the precipitated crystals were isolated, and recrystallized from ethyl acetate. 7.18 g (54%) of 5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine of melting point 188°-189° C. were obtained. 1H-NMR (CDCl3 270 MHz): δ4.7 (s, 2H), 6.9 (s, 1H), 8.1 (m, 4H), 9.1 (s, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04725689uspto-grants-1988_02