반응 #64277

ord-0d1412ab4e3b409890ef460da4092292

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05412095uspto-grants-1995_05