
Bufotenine (1, 5-hydroxy-N,N-dimethyltryptamine) was isolated from seeds of Anadenanthera spp., a tree widespread in the Brazilian cerrado, using an efficient acid-base shakeout protocol. The conversion of bufotenine into N,N-dimethyltryptamine (4) and 5-methoxy-N,N-dimethyltryptamine (5) was accomplished through an innovative and short approach featuring the use of novel bufotenine-aminoborane complex (7). Furthermore, an easy methodology for conversion of bufotenine into 5-hydroxy-N,N,N-trimethyltryptamine (6) was well-established. This is the first study that highlights bufotenine as a resource for the production of N,N-dimethyltryptamines for either pharmacological and toxicological investigations or for synthetic purposes.
Models, Molecular, Methoxydimethyltryptamines, Molecular Structure, Bufotenin, N,N-Dimethyltryptamine, Seeds, Fabaceae, Brazil
Models, Molecular, Methoxydimethyltryptamines, Molecular Structure, Bufotenin, N,N-Dimethyltryptamine, Seeds, Fabaceae, Brazil
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