Reaktion #50147

ord-19c9225c5e8a41bcafa33e80ae22cd3d

Reaktionsgleichung

CCOC(=O)C1NCCc2nc(CC)n(Cc3ccc(-c4ccccc4-c4nnnn4C(c4ccccc4)(c4ccccc4)c4ccccc4)cc3)c21
ethyl 2-ethyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate
CCOC(=O)CC(=O)[O-]
monoethyl malonate
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CCN(CC)CC
triethylamine
CCOC(=O)CC(=O)N1CCc2nc(CC)n(Cc3ccc(-c4ccccc4-c4nnn[nH]4)cc3)c2C1C(=O)OCC
ethyl 2-ethyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-5-ethoxycarbonylacetyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate
Ausbeute 67.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe reaction mixture is washed with water
  2. 2
    Trocknendried over sodium sulfate
  3. 3
    Sonstigeevaporated
  4. 4
    workup.DISSOLUTIONThe residue is dissolved in ethanol (30 ml)
  5. 5
    workup.ADDITIONfumaric acid (2.00 g) is added
  6. 6
    Temperaturthe solution is refluxed for three hours
  7. 7
    SonstigeThe solvent is evaporated
  8. 8
    workup.ADDITIONthe residue is treated with a saturated sodium hydrogen carbonate solution
  9. 9
    Extraktionextracted with chloroform
  10. 10
    SonstigeThe organic layer is dried
  11. 11
    Sonstigeevaporated
  12. 12
    SonstigePurification by silica gel column chromatography (solvent; chloroform/methanol)

Vorschrift

A solution of ethyl 2-ethyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (1.94 g), monoethyl malonate (0.74 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.80 g), triethylamine (1.40 g) in dichloromethane (20 ml) is stirred overnight at room temperature. The reaction mixture is washed with water and dried over sodium sulfate, and then evaporated. The residue is dissolved in ethanol (30 ml), fumaric acid (2.00 g) is added, and the solution is refluxed for three hours. The solvent is evaporated and the residue is treated with a saturated sodium hydrogen carbonate solution and then extracted with chloroform. The organic layer is dried and evaporated. Purification by silica gel column chromatography (solvent; chloroform/methanol) gives ethyl 2-ethyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-5-ethoxycarbonylacetyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (1.07 g) as a foam.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05424316uspto-grants-1995_06