Diisopropylethylamine → 3-Fluoro-4-(4-ethyl-3-oxopiperazin-1-yl)nitrobenzene

HRID 1108577ノート

反応式

HRID 1108577 の反応式
[CH2:1]([N:3]1[CH2:8][CH2:7][NH:6][CH2:5][C:4]1=[O:9])[CH3:2].C(N(CC)C(C)C)(C)C.[F:19][C:20]1[CH:21]=[C:22]([N+:27]([O-:29])=[O:28])[CH:23]=[CH:24][C:25]=1F.FC(F)(F)C(O)=O.C(N(CC)C(C)C)(C)C>C(#N)C>[F:19][C:20]1[CH:21]=[C:22]([N+:27]([O-:29])=[O:28])[CH:23]=[CH:24][C:25]=1[N:6]1[CH2:7][CH2:8][N:3]([CH2:1][CH3:2])[C:4](=[O:9])[CH2:5]1

参加物

6

実験手順

1-Ethyl-2-oxopiperazine (3TFA salt, 10.5 g) was dissolved in acetonitrile (200 ml), and N,N-diisopropylethylamine (19.5 ml) followed by 3,4-difluoronitrobenzene (2.25 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-ethyl-3-oxopiperazin-1-yl)nitrobenzene as a solid (3.44 g).

後処理

  1. additionwere added
  2. temperatureThe mixture was heated
  3. temperatureto reflux for 18 hours
  4. customSolvent was evaporated
  5. customthe residue chromatographed on silica using as eluant
  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

出典と根拠

ORDレコード
ord-e6d6bb280fdc4ebf98f0251e68132f1e
出典データセット
uspto-grants-2000_05
特許番号
US06069145

反応ノート

読み込み中…