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213ChemInform Abstract The condensation product (III) of α-methyltryptamine (I) and veratraldehyde (II) is alkylated by the chloroalkanoic amides (IV) to yield the amides (V) which are reduced, forming the amines (VI). The psychotropic activity of the compounds synthesized is tested. (IR-, NMR-data).

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The reaction product (III) of the tetrahydro‐β‐carboline (I) and epichlorohydrin (II) is converted to the aminopropanol derivatives (V) and their dihydrochlorides.