Benzylated PDE4 inhibitors
The present invention is directed to a method for reducing the emetogenic effects of PDE inhibitors, and more particularly is directed to compounds having PDE4 inhibition activity with little or no emetogenic side-effects, and chemical methods including benzylation for preparing such compounds. A benzyl group may be attached to either a carbon or nitrogen atom of a PDE4 inhibitor. Suitable benzylation chemistry is to extract a hydrogen from a PDE4 inhibitor, preferably with a base, and then react the resulting nucleophilic PDE4 inhibitor with a benzylating agent, e.g., benzyl bromide or a derivative thereof.
1. A compound having the following formula:
wherein:
Bzl is a benzyl group of the formula
wherein each of the numerals 1, 2, 3, 4 and 5 is carbon, with the proviso that the ring is aromatic; and
n is 5 and R 1 at each occurrence is independently selected from halogen, nitro, R 2 , and OR 2 wherein and R 2 at each occurrence is independently selected from H, C 1 -C 8 alkyl, alkoxyalkyl having 3-7 carbons in the alkoxy portion and 2-4 carbons in the alkyl portion, phenoxyalkyl having 2-6 carbons in the alkyl portion, C 3 -C 7 cycloalkyl, C 6 -C 9 polycycloalkyl, alkylcycloalkyl, hydroxyalkyl, carboxylate, alkylcarboxylate, carboxyl, alkyl carboxyl, amide, alkylamide, phenyl, phenylalkyl having 1-8 carbons in the alkyl portion, phenylaminoalkyl having 2-6 carbons in the alkyl portion and the amino may be optionally substituted with C 1 -C 4 alkyl and indanyl; wherein the alkyl portion of an R 2 group may be optionally substituted with one or more fluorine atoms, hydroxyl or C 1 -C 8 alkoxy; and the phenyl portion of an R 2 group may be optionally substituted with C 1 -C 8 alkyl, C 1 -C 8 alkoxy or halogen.