Ethanol → 4-Ethyl-6-methoxy-1,2,3,4-tetrahydroisoquinoline

HRID 1633880Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1633880
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]([CH2:12][CH3:13])[CH2:10][NH2:11])[CH:6]=[CH:7][CH:8]=1.C=O.[OH-].[K+].[CH2:18](O)C>C(O)=O>[CH2:12]([CH:9]1[C:5]2[C:6](=[CH:7][CH:8]=[C:3]([O:2][CH3:1])[CH:4]=2)[CH2:18][NH:11][CH2:10]1)[CH3:13]

Komponenten

6

Edukt 4

HCID 702EthanolHCID 712FormaldehydeHCID 14797Potassium HydroxideHCID 145280732-(3-Methoxyphenyl)butan-1-amine

Produkt 1

HCID 186800734-Ethyl-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 284Formic AcidLösungsmittel

Versuchsvorschrift

A solution of 2-(3-methoxyphenyl)-1-butanamine (25 g, 131 mmol, prepared according to the procedure described in J. Med. Chem. 1990, 33, 153-160) in formic acid (120 mL) at room temperature was treated with paraformaldehyde (4.18 g, 131 mmol), stirred for 16 hours, treated with 25% KOH (30 mL) and ethanol (100 mL), and refluxed for 2.5 hours. The mixture was cooled to room temperature, extracted with dichloromethane, and the combined extracts were dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with dichloromethane to provide the desired product.

Aufarbeitung

  1. temperaturerefluxed for 2.5 hours
  2. extractionextracted with dichloromethane
  3. dry with materialthe combined extracts were dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe concentrate was purified by flash column chromatography on silica gel with dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-79184d3f718c4a2398fdadd987c32f79
Quelldatensatz
uspto-grants-2003_01
Patentnummer
US06504031B1

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