Reaction #78454

ord-92ff14d55bef43148911363873a59fd9

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

Following the same procedure as that described in example 1E, 6-bromo-4-(3-ethoxy-phenyl)-2-methoxy-quinoline (400 mg, 1.11 mmol) and di-pyridin-3-yl-methanone (225 mg, 1.22 mmol) generated the title compound of 37A (212 mg, 41.2% yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06710209B2uspto-grants-2004_03