Pyrroloindoles. 15. Synthesis of tryptamine analogs. 6,7-dihydro-3-(2-phthalimidoethyl)-1h,5h-pyrrolo[2,3-f]indole and 3-(2-phthalimidoethyl)-1H,5H-pyrrolo[2,3-f]indole

Autor: Kadzhrishvili, D. O., Gordeev, E. N., Samsoniya, Sh. A., Suvorov, N. N.
Zdroj: Chemistry of Heterocyclic Compounds; February 1994, Vol. 30 Issue: 2 p188-191, 4p
Abstrakt: Diazotization of 1-acetyl-S-aminoindoline and reaction of the diazonium salt with ethyl a-acetyl-d-phthalimidovalerate gave the 1-acetyl-5-iruiolhgl hydrazone of ethyl a-keto-d-phthalimidovalerate. Cyclization of the hydrazone and subsequent hydrolysis, decarboxylation, and dehydrogenation of the pyrroloiruloline gave the corresponding tryptamines.
Databáze: Supplemental Index