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Gram-scale, chemoselective synthesis of N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-2-oxopiperidine-3-carboxamide (HIOC).
Setterholm, Noah A; McDonald, Frank E; Boatright, Jeffrey H; Iuvone, P Michael.
Afiliação
  • Setterholm NA; Department of Chemistry, Emory University, 1515 Dickey Drive NE, Atlanta, GA 30322 USA.
  • McDonald FE; Department of Chemistry, Emory University, 1515 Dickey Drive NE, Atlanta, GA 30322 USA.
  • Boatright JH; Department of Ophthalmology, Emory University School of Medicine, 1365B Clifton Road NE, Atlanta, GA 30322 USA ; Rehabilitation R & D Center, Atlanta VA Medical Center, Decatur, GA USA 30033 USA.
  • Iuvone PM; Department of Ophthalmology, Emory University School of Medicine, 1365B Clifton Road NE, Atlanta, GA 30322 USA ; Department of Pharmacology, Emory University School of Medicine, 1510 Clifton Road NE, Atlanta, GA 30322 USA.
Tetrahedron Lett ; 56(23): 3413-3415, 2015 Jun 03.
Article em En | MEDLINE | ID: mdl-26028783
N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-2-oxopiperidine-3-carboxamide (HIOC) is a potent activator of the TrkB receptor in mammalian neurons and of interest because of its potential therapeutic uses. In the absence of a commercial supply of HIOC, we sought to produce several grams of material. However, a synthesis of HIOC has never been published. Herein we report the preparation of HIOC by the chemoselective N-acylation of serotonin, without using blocking groups in the key acylation step.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article