Reacción #66869

ord-1f664c3939164f5cb0b90f35d5bd664b

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto yield 75 mg (56%)

Procedimiento

In analogy to Example 89, the title compound was prepared from N-(3,4-dichlorophenyl)-5,6,7,8-tetrahydropyrido[4′,3′:4,5]furo[2,3-d]pyrimidin-4-amine from Example 41A (100 mg, 0.30 mmol) and (2E)-4-(dimethylamino)but-2-enoic acid hydrochloride from Example 1A (69 mg, 0.42 mmol) to yield 75 mg (56%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524722B2uspto-grants-2013_09