반응 #93280

ord-a7d385ad8eba4da9bf9d492fd1a5c7a1

반응 방정식

O=Cc1ccc(OCC(=O)O)cc1
Compound A
O=Cc1ccc(OCC(=O)O)cc1
4-(Carboxymethyloxy)benzaldehyde
CCCn1c(N)c(N)c(=O)n(CCC)c1=O
5,6-diamino-1,3-dipropyluracil
CCCn1c(N)c(N=Cc2ccc(OCC(=O)O)cc2)c(=O)n(CCC)c1=O
6-Amino-1,3-dipropyl-5-(4'-carboxymethyloxybenzylideneamino)uracil

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A representative synthesis of benzylidene adduct
  2. 2
    온도After heating 15 minutes
  3. 3
    기타the volume was reduced by evaporation until crystallization
  4. 4
    workup.ADDITIONEther (40 ml) was added
  5. 5
    기타the nearly white solid was collected

실험 절차

A representative synthesis of benzylidene adduct is given. Compound A (1.51 g, 8.37 mmol) was dissolved in a mixture of methanol (35 ml) and acetic acid (5 ml) in a 50 ml boiling flask on a steam bath. To this was added a methanolic solution (60 ml) of freshly synthesized 5,6-diamino-1,3-dipropyluracil. After heating 15 minutes, the volume was reduced by evaporation until crystallization occurred. Ether (40 ml) was added and the nearly white solid was collected. Yield 2.80 g (86%), mp 179°-180° C. Analysis (C19H24N4O5): calc. 58.60% C, 6.21% H, 14.39% N; found 58.72% C, 6.16% H, 14.43% N.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04612315uspto-grants-1986_09