Sulfur analogs of psychotomimetic amines

✍ Scribed by David E. Nichols; Alexander T. Shulgin

• Book ID: 102404889
• Publisher: John Wiley and Sons
• Year: 1976
• Tongue: English
• Weight: 372 KB
• Volume: 65
• Category: Article
• ISSN: 0022-3549
• DOI: 10.1002/jps.2600651040

✦ Synopsis

The syntheses and physical properties are described for 2,5-dimethoxy-4-methylthiophenylethylamine and 2,5-dimethoxy-4-methylthiophenylisopropylamine. The latter compound is the sulfur analog of the psychotomimetic phenylisopropylamines 2,4,5-trimethoxyphenylisopropylamine and 2.5-dimethoxy-4-methylphenylisopropylamine wherein the methylthio group replaces a methoxy group or a methyl group, respectively. This compound is predicted to be about 30 times as active as mescaline.

Keyphrases Amines, phenylalkyl, substituted-sulfur analogs of psychotomimetic agents synthesized Sulfur analogs-psychotomimetic substituted phenylalkylamines synthesized 0 Psychotomimetic agents, potential-sulfur analogs of substituted phenylalkylamines synthesized Also referred to as DOM and STP. N M R spectra were obtained on a Varian A-60 or EM-360 spectrometer. IR mectra were obtained usine a Beckman IR-18. Melting w i n s were determined -. iA open glass capillaries acd are uncorrected. 3 Celite.