반응 #327473

ord-ef26d88e0aad42ae88e8a23b6ba642bf

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was heated
  2. 2
    온도at reflux for 36 h
  3. 3
    기타Most of the solvent was evaporated
  4. 4
    workup.ADDITIONThe resulting residue was diluted with water (300 mL)
  5. 5
    추출extracted with EtOAc (250 mL×2)
  6. 6
    세척The extracts were washed with brine
  7. 7
    건조dried over MgSO4
  8. 8
    농축concentrated
  9. 9
    기타to give a mixture, which
  10. 10
    기타was separated by silica gel column
  11. 11
    세척eluted with 20-30% ethyl acetate in petroleum ether

실험 절차

To a solution of MeONa (0.82 M) in methanol (200 mL), freshly prepared from sodium (3.80 g, 165 mmol) and dry methanol (200 mL), was added methyl 2-(2-(2-chloro-5-fluorobenzylcarbamothioyl)hydrazono)propanoate (28, 10.00 g, 31.5 mmol). The mixture was heated at reflux for 36 h. Most of the solvent was evaporated. The resulting residue was diluted with water (300 mL), acidified with 2 N HCl to pH=1˜2, and then extracted with EtOAc (250 mL×2). The extracts were washed with brine, dried over MgSO4, and concentrated to give a mixture, which was separated by silica gel column, and eluted with 20-30% ethyl acetate in petroleum ether to give 4-(2-chloro-5-fluorobenzyl)-6-methyl-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one (29).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08648073B2uspto-grants-2014_02