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Isoquinolin-3-Amine → 5,6,7,8-Tetrahydroisoquinolin-3-amine

HRID 1740970
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1740970
[NH2:1][C:2]1[N:3]=[CH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[H][H]>FC(F)(F)C(O)=O.[Pt]=O>[NH2:1][C:2]1[N:3]=[CH:4][C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 311869Isoquinolin-3-AmineHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 133023975,6,7,8-Tetrahydroisoquinolin-3-amineAusbeute 34 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 82844Platinum oxide (PtO)KatalysatorHCID 6422Trifluoroacetic acidLösungsmittel

Versuchsvorschrift

Using the method of Example 63, Step A, 75 mg of 3-aminoisoquinoline (7.73 mmoles) and 8.7 mg platinum oxide in 2 mL of trifluoroacetic acid was shaken under 40 psi of hydrogen for 3 h. The mixture was filtered and catalyst was washed with ethyl acetate. After concentrating the filtrate, the residue was dissolved in 10 mL of ethyl acetate and washed with 5 mL of saturated aquous sodium bicarbonate. The organic solution was dried (sodium sulfate), decanted, and concentrated to give a yellow syrup. Flash coumn chromatography on 19 g of silica gel, eluting with 600 mL of 50% ethyl acetate/hexane gave 26.5 mg (34% yield) of 3-amino-5,6,7,8-tetrahydroisoquinoline as a pale yellow solid.

Aufarbeitung

  1. filtrationThe mixture was filtered
  2. washcatalyst was washed with ethyl acetate
  3. concentrationAfter concentrating the filtrate
  4. dissolutionthe residue was dissolved in 10 mL of ethyl acetate
  5. washwashed with 5 mL of saturated aquous sodium bicarbonate
  6. dry with materialThe organic solution was dried (sodium sulfate)
  7. customdecanted
  8. concentrationconcentrated
  9. customto give a yellow syrup
  10. washFlash coumn chromatography on 19 g of silica gel, eluting with 600 mL of 50% ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-590e9480a04b43cd8fc401785bc627d0
Quelldatensatz
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05972975

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