Reacción #68957

ord-e655c65431ab438b8107c65886b84adc

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothose described in Synthesis 5-1
  2. 2
    Otrothe reaction at 140° C.

Procedimiento

The title compound was prepared using methods analogous to those described in Synthesis 5-1, replacing 3,8-dichloroisoquinoline with 5-(8-bromoisoquinolin-3-ylamino)pyrazine-2-carbonitrile and replacing (R)-5-amino-3-(pyrrolidin-3-yloxy)pyrazine-2-carbonitrile with N-(2-aminoethyl)morpholine, and conducting the reaction at 140° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08530468B2uspto-grants-2013_09