Reacción #93096

ord-a2e90dd09dc44e3eaf94f2fa50d32e67

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónWhen the catalyst was filtered off
  2. 2
    Concentraciónthe filtrate was concentrated

Procedimiento

In 150 ml of methanol was dissolved 782 mg of Nα -[(S)-2-azetidinone-4-carbonyl]-L-histidyl-L-proline benzyl ester (12) and the compound (12) was hydrogenated for 2 hours at room temperature using 156 mg of 10% palladium-carbon as a catalyst. When the catalyst was filtered off and the filtrate was concentrated, 620 mg of Nα -[(S)-2-azetidinone-4-carbonyl]-L-histidyl-L-proline (13) was obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04610821uspto-grants-1986_09