The Synthesis of Some Analogs of the Hallucinogen 1-(2,5-Dimethoxy-4-methyl-phenyl)-2-aminopropane (DOM). III. Some Derivatives of 3-phenylalanine
Ronald T. Coutts, Jerry L. Malicky
Canadian Journal of Chemistry February 1, 1974 DOI: 10.1139/v74-062 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Peer reviewed |
|---|---|
| Key points | Reports synthetic routes to the hydrochlorides of three dimethoxyphenylalanine derivatives and concludes that a related phenol (C10H14ClNO4) is a monohydrate of the lactone 3-amino-6-hydroxy-7-methyl hydrocoumarin hydrochloride. |
Abstract
Syntheses of the hydrochlorides of 3-(2,5-dimethoxyphenyl)alanine, 3-(2,5-dimethoxy-4-methylphenyl) alanine, and 3-(4-bromo-2,5-dimethoxyphenyl)alanine are described. A phenol, C10H14ClNO4, related to the second of these three compounds was also prepared and is concluded to be a monohydrate of the lactone, 3-amino-6-hydroxy-7-methyl hydrocoumarin hydrochloride.