Reaction #78455

ord-19887dc558144894847848b5693d0f22

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

Following the same procedure as described in example 1F, [4-(3-ethoxy-phenyl)-2-methoxy-quinolin-6-yl]-di-pyridin-3-yl-methanol (212 mg, 0.457 mmol) was treated with HCl in aqueous THF to yield the title compound (91 mg, 44.3% yield).

Source

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