반응 #69646

ord-0eb6d9ccbea645b387af24bfb3716cae

반응 방정식

Cc1cc(C)c(Nc2ncc(Br)c(Nc3ccc(C#N)cc3)n2)c(C)c1
intermediate 2
Cc1cc(C)c(Nc2ncc(Br)c(Nc3ccc(C#N)cc3)n2)c(C)c1
4-[[5-bromo-2-[(2,4,6-trimethylphenyl)amino]-4-pyrimidinyl]amino]benzonitrile
CCOCC
ether
N#Cc1ccc(N)cc1
4-aminobenzonitrile
C1COCCO1
1,4-dioxane
Cl
HCl
CCOCC
diethyl ether
Cc1cc(C)c(Nc2nc(Nc3ccc(C#N)cc3)ncc2Br)c(C)c1
4-[[5-bromo-4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile
수율 13.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was evaporated
  2. 2
    workup.ADDITION1,4-dioxane (20 ml) was added
  3. 3
    온도refluxed for seven days
  4. 4
    기타The solvent was evaporated
  5. 5
    workup.DISSOLUTIONthe residue dissolved in CH2Cl2
  6. 6
    세척washed with 1 M NaOH
  7. 7
    기타the solvent evaporated
  8. 8
    workup.DISSOLUTIONThe residue was dissolved in CH2Cl2 (10 ml)
  9. 9
    여과the precipitate was filtered off
  10. 10
    기타dried

실험 절차

To a flask containing intermediate 2 (0.00285 mop was added ether. To this homogeneous solution was added HCl in diethyl ether (1M; 0.00855 mol). The solvent was evaporated and 1,4-dioxane (20 ml) was added. Finally, 4-aminobenzonitrile (0.00291 mol) and 1,4-dioxane (15 ml) were added and the reaction mixture was stirred and refluxed for seven days. The solvent was evaporated, the residue dissolved in CH2Cl2, washed with 1 M NaOH, and the solvent evaporated. The residue was dissolved in CH2Cl2 (10 ml) and the precipitate was filtered off and dried, yielding 0.15 g (13%) of 4-[[5-bromo-4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile (comp. 3).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08530655B2uspto-grants-2013_09