Reacción #491712

ord-35bfe89916774882a1a23dcca66bb928

Ecuación de reacción

CCOCC
ether
CS(=O)(=O)O
methanesulphonic acid
N=C(N)NN.O=C(O)O
aminoguanidine bicarbonate
CS(=O)(=O)O.CS(=O)(=O)O.N=C(N)NN
Aminoguanidine Bismesylate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONWhen the addition
  2. 2
    Otrohad fallen to ˜40°
  3. 3
    workup.ADDITIONDuring the addition, colourless needles
  4. 4
    Filtraciónfiltered
  5. 5
    Lavadothe product washed with cold ether
  6. 6
    Otrodried overnight in vacuo at 50°
  7. 7
    OtroYield=528 g (99.25%), mpt=149-150° (Lit: WO/2004/026845; 147.5°)

Procedimiento

To a stirred solution of 99.5% methanesulphonic acid [Aldrich] (422 g; 4.40 mol) in methanol (720 cm3) at 40° was added portionwise over 30 minutes aminoguanidine bicarbonate [Aldrich] (272.0 g; 2.00 mol). When the addition was complete, the solution was stirred until the temperature had fallen to ˜40° and then treated slowly with cold ether (500 cm3). During the addition, colourless needles started to deposit. The resulting slurry was stood at 0° for 4 hrs, filtered and the product washed with cold ether and dried overnight in vacuo at 50°. Yield=528 g (99.25%), mpt=149-150° (Lit: WO/2004/026845; 147.5°)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08748599B2uspto-grants-2014_06