Reacción #66814

ord-084e91f3981f46cba9a252406bdee933

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto yield 443 mg (28%)

Procedimiento

In analogy to Example 38A, the title compound was prepared from ethyl 3-cyano-2-{[(1E)(dimethylamino)methylidene]amino}-4,7-dihydrofuro[2,3-c]pyridine-6(5H)-carboxylate from Example 37A (1.20 g, 4.14 mmol) and 3-ethynylaniline (968 mg, 8.27 mmol) to yield 443 mg (28%).

Fuente

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