Reaktion #66871

ord-24d12bd671954b968e16af9392f9ba57

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto yield 66 mg (46%)

Vorschrift

In analogy to Example 89, the title compound was prepared from N-(3-ethynylphenyl)-5,6,7,8-tetrahydropyrido[4′,3′:4,5]furo[2,3-d]pyrimidin-4-amine from Example 43A (100 mg, 0.344 mmol) and (2E)-4-(dimethylamino)but-2-enoic acid hydrochloride from Example 1A (80 mg, 0.48 mmol) to yield 66 mg (46%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524722B2uspto-grants-2013_09