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Trimethylsilyl cyanide → 2-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-ol

HRID 1033017
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1033017
[CH3:1][O:2][C:3]1[N:10]=[C:9]([CH3:11])[C:8]([CH2:12][CH3:13])=[CH:7][C:4]=1[CH:5]=[O:6].C[Si]([C:18]#[N:19])(C)C.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C(OCC)C.[I-].[Zn+2].[I-]>[CH3:1][O:2][C:3]1[C:4]([CH:5]([OH:6])[CH2:18][NH2:19])=[CH:7][C:8]([CH2:12][CH3:13])=[C:9]([CH3:11])[N:10]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 82115Trimethylsilyl cyanideHCID 102616792-Methoxy-5-ethyl-6-methylnicotinaldehydeHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 103307592-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-ol

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 9883512zinc(II)iodideKatalysator
HCID 3283
Diethyl Ether
Lösungsmittel
2×

Versuchsvorschrift

A mixture of 2-methoxy-5-ethyl-6-methylnicotinaldehyde (1.05 g, 5.86 mmol) and trimethylsilyl cyanide (0.85 mL, 6.37 mmol) containing zinc iodide (10 mg) was stirred, under a nitrogen atmosphere, at ambient temperature for two hours. This liquid was diluted with anhydrous diethyl ether, filtered and then added dropwise to a suspension of lithium aluminum hydride (225 mg, 5.9 mmol) in diethyl ether (15 mL) under nitrogen. After two hours the reaction was quenched with saturated aqueous sodium sulfate, diluted with methylene chloride, filtered and the solvents evaporated to give a semi-solid. This residue was triturated with cold diethyl ether and the crystalline product was collected by filtration to yield 346 mg (28%).

Aufarbeitung

  1. filtrationfiltered
  2. customAfter two hours the reaction was quenched with saturated aqueous sodium sulfate
  3. additiondiluted with methylene chloride
  4. filtrationfiltered
  5. customthe solvents evaporated
  6. customto give a semi-solid
  7. customThis residue was triturated with cold diethyl ether
  8. filtrationthe crystalline product was collected by filtration
  9. customto yield 346 mg (28%)

Quellen und Nachweise

ORD-Eintrag
ord-989f814f22c349e0b0631f4de664ba38
Quelldatensatz
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05308854

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