FARNESYL CHAIN MODIFICATION OF SQUALENE SYNTHASE INHIBITOR BENZYLFARNESYLAMINE - CONVERSION TO THE TERMINAL BIS(TRIFLUOROMETHYL) DERIVATIVE

Potent squalene synthase inhibitor 1 was converted to the bis(trifluor omethyl) analog 14 in 11% overall yield for 9 steps. The amine nitroge n of 1 was protected with the 2-(trimethylsilyl)ethoxycarbonyl (TEOC) protecting group. The 10,11 olefin was selectively epoxidized, cleaved and converted to the phosphonium salt 6. The ylid from 6 underwent a Wittig condensation with hexafluoroacetone to give the TEOC containing olefin 8. Tetrabutylammonium fluoride or HF could not remove the TEOC group without isomerizing the 10,11 olefin of the famesyl chain to th e E-9,10 olefin. The bis(trifluoromethyl) olefin of 8 is very sensitiv e to either acidic or basic conditions. However, it was found that BF3 .Et2O could remove the TEOC group without the undesired isomerization to give 14.