Reaktion #61533
ord-af17968064c44cdd8fde6f7fad4387b0
Reaktionsgleichung
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-furan-2-yl-1H -pyrazole-3-carboxylic acid
4-(4-Amino-phenyl)-morpholin-3-one
BOP-Cl
→
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
Edukte
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1EinengenThe mixture was was concentrated under reduced pressure
- 2Sonstigethe residue was purified by preparative HPLC (
- 3WaschenC18 reverse phase column, elution with a H2O/MeCN gradient with 0.1% TFA)
- 4workup.ADDITIONThe fractions containing the product
- 5Sonstigewere evaporated
- 6Sonstigeto 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.