Reaction #78446

ord-3c71e74672144d9a8e9da2c41d24fa42

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

The same procedure described in example 8, 6-[(6-chloro-pyridin-3-yl)-hydroxy-(3-methyl-3H-imidazol-4-yl)-methyl]-4-(3-ethoxy-phenyl)-1H-quinolin-2-one (50 mg, 0.103 mmol) and 1-bromo-2-methylpropane (0.022 ml, 0.206 mmol) generated the title compound as a white solid (24 mg, 40% yield).

Source

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