Reaktion #61533

ord-af17968064c44cdd8fde6f7fad4387b0

Reaktionsgleichung

O=C(O)c1cc(-c2ccco2)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-furan-2-yl-1H -pyrazole-3-carboxylic acid
Nc1ccc(N2CCOCC2=O)cc1
4-(4-Amino-phenyl)-morpholin-3-one
O=C1OCCN1P(=O)(Cl)N1CCOC1=O
BOP-Cl
O=C(Nc1ccc(N2CCOCC2=O)cc1)c1cc(-c2ccco2)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-furan-2-yl-1H-pyrazole-3-carboxylic acid [4-(3-oxo-morpholin-4-yl)-phenyl]-amide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe mixture was was concentrated under reduced pressure
  2. 2
    Sonstigethe residue was purified by preparative HPLC (
  3. 3
    WaschenC18 reverse phase column, elution with a H2O/MeCN gradient with 0.1% TFA)
  4. 4
    workup.ADDITIONThe fractions containing the product
  5. 5
    Sonstigewere evaporated
  6. 6
    Sonstigeto yield a white solid

Vorschrift

To 100 mg 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-furan-2-yl-1H -pyrazole-3-carboxylic acid in 2 ml DCM and 0.1 ml NEt3, 62 mg 4-(4-Amino-phenyl)-morpholin-3-one and 67 mg BOP-Cl were added at RT and the mixture was stirred for 16 h. The mixture was was concentrated under reduced pressure and the residue was purified by preparative HPLC (C18 reverse phase column, elution with a H2O/MeCN gradient with 0.1% TFA). The fractions containing the product were evaporated and lyophilized to yield a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07429581B2uspto-grants-2008_09