Diisopropylethylamine → 3-Fluoro-4-(4-{2-methoxyethyl}-3-oxopiperazin-1-yl)nitrobenzene

HRID 1108585Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1108585
[CH3:1][O:2][CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][NH:8][CH2:7][C:6]1=[O:11].C(N(CC)C(C)C)(C)C.[F:21][C:22]1[CH:23]=[C:24]([N+:29]([O-:31])=[O:30])[CH:25]=[CH:26][C:27]=1F.FC(F)(F)C(O)=O.C(N(CC)C(C)C)(C)C>C(#N)C>[F:21][C:22]1[CH:23]=[C:24]([N+:29]([O-:31])=[O:30])[CH:25]=[CH:26][C:27]=1[N:8]1[CH2:9][CH2:10][N:5]([CH2:4][CH2:3][O:2][CH3:1])[C:6](=[O:11])[CH2:7]1

Komponenten

6

Versuchsvorschrift

1-(2-Methoxyethyl)-2-oxopiperazine (4TFA salt, 13.5 g) was dissolved in acetonitrile (200 ml), and N,N-diisopropylethylamine (22.6 ml) followed by 3,4-difluoronitrobenzene (2.2 ml) were added. The mixture was heated to reflux for 18 hours. Solvent was evaporated, and the residue chromatographed on silica, using as eluant a gradient increasing in polarity from 0 to 4% methanol in dichloromethane. Relevant fractions were combined and evaporated to give a solid containing some N,N-diisopropylethylamine trifluoroacetate. The solid was purified by dissolving in ethyl acetate and washing well with water. Evaporation of the organic layer gave 3-fluoro-4-(4-{2-methoxyethyl}-3-oxopiperazin-1-yl)nitrobenzene as a solid (4.07 g).

Aufarbeitung

  1. additionwere added
  2. temperatureThe mixture was heated
  3. temperatureto reflux for 18 hours
  4. customSolvent was evaporated
  5. customthe residue chromatographed on silica
  6. temperaturea gradient increasing in polarity from 0 to 4% methanol in dichloromethane
  7. customevaporated
  8. customto give a solid
  9. customThe solid was purified
  10. dissolutionby dissolving in ethyl acetate
  11. washwashing well with water
  12. customEvaporation of the organic layer

Quellen und Nachweise

ORD-Eintrag
ord-0793201206914d67a7c39c99a9472194
Quelldatensatz
uspto-grants-2000_05
Patentnummer
US06069145

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