Reacción #64277

ord-0d1412ab4e3b409890ef460da4092292

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrog, 16.0 mmol, prepared in accordance with the teachings of U.S
  2. 2
    workup.DISSOLUTIONThe solid initially dissolved
  3. 3
    Otroa precipitate formed
  4. 4
    FiltraciónThe precipitate was collected by filtration
  5. 5
    Lavadowashed with a small quantity of dry methanol

Procedimiento

1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-(tetrahydro-2-furoyl)piperazine monohydrochloride dihydrate (7.37. g, 16.0 mmol, prepared in accordance with the teachings of U.S. Pat. No. 4,25 1,532) was placed in an Edenmeyer flask and dissolved in a minimum amount (about 10 mL) of hot dry methanol. The solid initially dissolved, but soon turned cloudy and a precipitate formed. The precipitate was collected by filtration and washed with a small quantity of dry methanol followed by dry acetone to yield 6.35 g (13.9 mmol, 87.0%) of 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(tetrahydro-2-furoyl)piperazine monohydrochloride methanolate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05412095uspto-grants-1995_05