Synthetic processes for the preparation of aminocyclohexyl ether compounds
This invention is directed to stereoselective synthesis of compounds of formula (I) or formula (II): or a pharmaceutically acceptable salt, ester, amide, complex, chelate, clathrate, solvate, polymorph, stereoisomer, metabolite or prodrug thereof; wherein R 3 , R 4 and R 5 are defined herein. Compounds of formula (I) and formula (II) are known to be useful in treating arrhythmias.
1. A method of making a compound of formula (I):
or a pharmaceutically acceptable salt, ester, amide, clathrate with a cyclodextrin or solvate in a solution phase thereof; or a single stereoisomer or mixture thereof;
wherein:
R 3 , R 4 and R 5 are independently bromine, chlorine, fluorine, carboxy, hydrogen, hydroxy, hydroxymethyl, methanesulfonamido, nitro, cyano, sulfamyl, trifluoromethyl, —CHF 2 , —SO 2 N(R 8 )R 9 , —OCF 3 , C 2 -C 7 alkanoyloxy, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 7 -C 12 aralkoxy, C 2 -C 7 alkoxycarbonyl, C 1 -C 6 thioalkyl, aryl or —N(R 6 )R 7 ; and
R 6 , R 7 , R 8 , and R 9 are each independently selected from hydrogen, acetyl, methanesulfonyl or C 1 -C 6 alkyl;
which method comprises the following:
a) reacting a compound of formula (1a):
with a compound of formula (2a):
under suitable condensation conditions to form a product;
b) reacting the product of a) with a compound of formula (5):
wherein Q is a leaving group and R 3 , R 4 and R 5 are as defined above, under suitable ether coupling conditions to form a product;
c) reacting the product of b) under suitable cyclization conditions to form a compound of formula (6):
wherein each R 2a is O or H 2 where at least one R 2a is O, R is H, C 2 -C 5 acyl or an oxygen-protecting group and R 3 , R 4 and R 5 are as defined above; and
d) reducing the compound of formula (6) under suitable conditions to form a compound of formula (I), as set forth above;
e) optionally treating the compound of formula (I) with a suitable reagent or solvent to form the pharmaceutically acceptable salt, ester, amide, clathrate with a cyclodextrin or solvate in a solution phase thereof.
2. The method of claim 1 wherein the product of a) comprises a compound of formula (9), a compound of formula (10) or a mixture of a compound of formula (9) and a compound of formula (10):
where each R 2a is O or H 2 and R is H, C 2 -C 5 acyl or an oxygen-protecting group.
3. The method of claim 1 or claim 2 wherein the product of b) comprises a compound of formula (11), a compound of formula (12) or a mixture of a compound of formula (11) and a compound of formula (12):
where each R 2a is O or H 2 , R is H, C 2 -C 5 acyl or an oxygen-protecting group and R 3 , R 4 and R 5 are as defined above.
4. The method of claim 1 further comprising the formation of an acid addition salt of the compound of formula (I).
5. The method of claim 1 wherein the compound of formula (I) is a compound of formula (I) where R 3 , R 4 and R 5 are independently hydrogen, hydroxy or C 1 -C 6 alkoxy; with the proviso that R 3 , R 4 and R 5 cannot all be hydrogen at the same time.
6. The method of claim 5 wherein the compound of formula (I) is a compound of formula (Ia):
or a pharmaceutically acceptable salt, ester, amide, clathrate with a cyclodextrin or solvate in a solution phase thereof.
7. The method of claim 5 wherein the compound of formula (I) is selected from the group consisting of:
or pharmaceutically acceptable salts, esters, amides, clathrates with cyclodextrin or solvates in solution phase thereof.