Reaktion #61536

ord-028c8038433b40b496f5b00080a16d09

Reaktionsgleichung

O=C(O)c1cc(CO)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-hydroxymethyl-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(CO)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-hydroxymethyl-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 concentrated under reduced pressure
  2. 2
    Sonstigetriturated in a mixture of water/DMF
  3. 3
    FiltrationThe precipitate was collected by filtration
  4. 4
    Waschenwashed with water containing 0.5% TFA
  5. 5
    SonstigeThe product was obtained as a white solid which
  6. 6
    Sonstigewas dried under reduced pressure

Vorschrift

To 100 mg 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-hydroxymethyl-1H-pyrazole-3-carboxylic acid in 2 ml DCM and 0.1 ml NEt3, 67 mg 4-(4-Amino-phenyl)-morpholin-3-one and 74 mg BOP-Cl were added at RT and the mixture was stirred for 16 h. The mixture was concentrated under reduced pressure and triturated in a mixture of water/DMF. The precipitate was collected by filtration and washed with water containing 0.5% TFA. The product was obtained as a white solid which was dried under reduced pressure.

Quelle

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