Water → (2 Aminoeth 1-yl) 4-naphth-1-ylpiperidine

HRID 1197877

Reaktionsgleichung

Reaktionsgleichung von HRID 1197877
[H-].[Al+3].[Li+].[H-].[H-].[H-].Cl.[C:8]1([CH:18]2[CH2:23][CH2:22][N:21]([CH2:24][C:25]#[N:26])[CH2:20][CH2:19]2)[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=1.O.[OH-].[Na+]>O1CCCC1>[NH2:26][CH2:25][CH2:24][N:21]1[CH2:22][CH2:23][CH:18]([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]=[CH:10][CH:9]=2)[CH2:19][CH2:20]1

Komponenten

6

Versuchsvorschrift

1.75 g of lithium aluminum hydride are added in fractions under a stream of nitrogen to a solution of 4.4 g of the compound from Example 4 in 150 ml of tetrahydrofuran. After stirring for 1 hour, the mixture is hydrolyzed with 1.75 ml of water, 3.5 ml of a 10% (wt/wt) sodium hydroxide solution and 7 ml of water. Filtration through celite, followed by evaporation of the solvent, yields an oily product which is used as it is in the following stage.

Aufarbeitung

  1. filtrationFiltration through celite
  2. customfollowed by evaporation of the solvent
  3. customyields an oily product which

Quellen und Nachweise

ORD-Eintrag
ord-3ba964bb8dea44cb8682166389a402b8
Quelldatensatz
uspto-grants-1994_01
Patentnummer
US05278185

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