AbstractDurch Alkylierung der Piperazine und Homopiperazine (II) bzw. (IV) mit Trimethoxyphenylethylchlorid (I) erhält man die sedativ wirksamen Mescalinderivate (III) und (V).
Structural juxtaposition of the 3,4,5-trimethoxyphenyl group in the same molecule with a piperazine or homopiperazine ring has been realized in a series of mescaline analogues (I-IV) as part of an investigation into the pharmacological properties of the seven-membered perhydro-1,4-diazepines (homopiperazines). The analogous six-membered piperazines were synthesized and tested as reference...