반응 #4785

ord-1b0e899e852c46f697084b105512427c

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축the reaction mixture was concentrated under reduced pressure
  2. 2
    여과The precipitate was collected by filtration
  3. 3
    세척washed with water
  4. 4
    기타dried in vacuo

실험 절차

To a mixture of 6-methyl-5-(1-piperazinylmethyl)-4-(3-nitrophenyl)-2-phenylpyrimidine dihydrochloride (1 g), dichloromethane (10 ml) and triethylamine (0.48 g), was added 2-furoyl chloride (0.31 g) at 5° C. under ice cooling. After stirring for 1 hour at the same temperature, the reaction mixture was concentrated under reduced pressure. The residue was suspended in water and adjusted to pH=9 with aqueous saturated sodium hydrogen carbonate. The precipitate was collected by filtration, washed with water and dried in vacuo to give 6-methyl-5-[4-(2-furoyl)piperazin-1-ylmethyl]-4-(3-nitrophenyl)-2-phenylpyrimidine (1.02 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04727073uspto-grants-1988_02