Synthetic methods and intermediates for the preparation of xenicanes
The invention provides novel synthetic intermediates and synthetic methods that are useful for preparing compounds of the xenicane family. Certain compounds of the invention may also possess anti-cancer properties.
1. A compound of formula 1:
wherein:
R a is H, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, aryl, or heteroaryl, wherein each (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 3 -C 8 )cycloalkyl, and (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl of R a is optionally substituted with one or more groups independently selected from halo, hydroxy, cyano, nitro, (C 1 -C 6 )alkoxy, (C 3 -C 8 )cycloalkyl, oxo, carboxy, aryl, aryloxy, and —NR b R c ; and wherein each aryl, and heteroaryl of R a is optionally substituted with one or more groups independently selected from (C 1 -C 6 )alkyl, halo, hydroxy, cyano, carboxy, nitro, trifluoromethyl, trifluoromethoxy, (C 1 -C 6 )alkoxy, (C 1 -C 6 )alkoxycarbonyl, (C 1 -C 6 )alkanoyloxy, and —NR b R c ; and
R b and R c are each independently selected from H, (C 1 -C 6 )alkyl, (C 3 -C 8 )cycloalkyl, (C 3 -C 8 )cycloalkyl(C 1 -C 6 )alkyl, aryl, heteroaryl, aryl(C 1 -C 6 ) alkyl and heteroaryl(C 1 -C 6 )alkyl; or R b and R c together with the nitrogen to which they are attached form a aziridino, azetidino, morpholino, piperazino, pyrrolidino or piperidino.
2. A method for preparing an ester of formula 1:
wherein R a is methyl;
comprising treating an acid of formula 2:
with (Me) 2 SiCHN 2 in methanol at about 0° C. to provide the ester of formula 1.
3. A compound of formula 2, 10, 11b, 12, 13, 20, 23, 24, 25, 26, or 27: