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Abstract
Se prepara 3-alquil-4-amino-2-metil-4,5,6,7-tetrahidroindol (lll) por reducción de 3-alquil-4-hidroxiimino-2-metil-4,5,6,7-tetrahidroindol (H) con Zn/AcOH. El compuesto II se ha obtenido por condensación de 3-alquil-2-metil-4-oxo-4,5,6,7-tetrahidroindol (I) con hidroxilamina. La reacción del compuesto (lll) con N-(2-cloroetil)-N,N-dimetilamina dá 3-alquil-4-[(2-dimetilarninoetil)arnino]-2-metil-4,5,6,7-tetrahidroindol (IV).
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