Reaktion #46789

ord-79f71b05143e49688872fd3f6a5d773c

Reaktionsgleichung

O=C(O)c1nc2ccccc2[nH]1
1H-Benzoimidazole-2-carboxylic acid
NC1CCN(c2ccncn2)CC1.O=C(O)C(F)(F)F
1-Pyrimidin-4-yl-piperidin-4-ylamine trifluoroacetate
O=C1OCCN1P(=O)(Cl)N1CCOC1=O
BOP-Cl
O=C([O-])O.[Na+]
NaHCO3
O=C(NC1CCN(c2ccncn2)CC1)c1nc2ccccc2[nH]1
1H-Benzoimidazole-2-carboxylic acid (1-pyrimidin-4-yl-piperidin-4-yl)-amide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe mixture was filtered through a chem elut® cartridge by elution with ethyl acetate
  2. 2
    SonstigeAfter removal of the solvent under reduced pressure the crude product
  3. 3
    Sonstigewas subjected to the next reaction step without further purification

Vorschrift

To a solution of 80 mg 1H-Benzoimidazole-2-carboxylic acid in 1 mL DMF and 0.2 mL NEt3, 200 mg 1-Pyrimidin-4-yl-piperidin-4-ylamine trifluoroacetate and 125 mg BOP-Cl were added and the mixture was stirred for 3 h. Finally, 3 mL saturated NaHCO3 solution were added and the mixture was filtered through a chem elut® cartridge by elution with ethyl acetate. After removal of the solvent under reduced pressure the crude product was subjected to the next reaction step without further purification. Yield: 160 mg.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741341B2uspto-grants-2010_06