Reacción #95016

ord-3793e228fe1f42c4bf7da6b6768a2b83

Ecuación de reacción

Cc1cnc(N)cn1
2-amino-5-methylpyrazine
BrBr
bromine
[Na+].[OH-]
sodium hydroxide
CC(=O)[O-].O.O.O.[Na+]
sodium acetate trihydrate
Cc1cnc(N)c(Br)n1
2-Amino-3-bromo-5-methylpyrazine

Condiciones de reacción

Temperatura
20°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat 2° C.
  2. 2
    workup.ADDITIONpoured into ice
  3. 3
    Filtraciónfiltered
  4. 4
    Extracciónresidue extracted with ether
  5. 5
    Otrothe 2-amino-3-bromo-5-methylpyrazine crystallized from a suitable solvent

Procedimiento

To acetic acid (1500 ml.), 2-amino-5-methylpyrazine (1 mole) and 326.5 g. sodium acetate trihydrate are slowly added 1.1 mole bromine in 180 ml. acetic acid at 2° C. in the absence of light. The mixture is stirred about 15 hours at 20° C., stripped of acetic acid in vacuo, poured into ice, made alkaline with sodium hydroxide, filtered, and residue extracted with ether, the extract stripped and the 2-amino-3-bromo-5-methylpyrazine crystallized from a suitable solvent.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04343802uspto-grants-1982_08