Cyclobutanamine, hydrochloride (1:1) → N-Cyclobutyl-6-[1-hydroxy-1-(1H-imidazol-4-yl)-2-methylpropyl)-2-naphthamide

Participants

Reaction Steps

In a manner to that described in Example 9-(i), methyl 6-(1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl)-2-naphthoate (1.78 g) was converted to 6-(1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl)-2-naphthoic acid, which was reacted with cyclobutylamine hydrochloride (405 mg) in a similar manner as described in Example 24-(i) to give the titled compound (1.36 g) as a colorless powder.

Provenance & Evidence