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Triethylsilane → (S)-2-amino-4,4-difluoro-pentanoic acid methyl ester

HRID 19309
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 19309
[CH3:1][O:2][C:3](=[O:21])[C@@H:4]([NH:10]C(OCC1C=CC=CC=1)=O)[CH2:5][C:6]([F:9])([F:8])[CH3:7].C([SiH](CC)CC)C>[Pd].CO>[CH3:1][O:2][C:3](=[O:21])[C@@H:4]([NH2:10])[CH2:5][C:6]([F:9])([F:8])[CH3:7]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 12052Triethylsilane3×HCID 57535380HCID 57535380, Verbindung

Produkt 1

HCID 57946221(S)-2-amino-4,4-difluoro-pentanoic acid methyl esterAusbeute 43,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysator3×HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

In a flask under argon was placed (S)-2-benzyloxycarbonylamino-4,4-difluoro-pentanoic acid methyl ester (626 mg, 2.08 mmol), methanol (8 mL) and 10% palladium on activated carbon (100 mg). Triethylsilane (3 mL) was added slowly and the mixture stirred at 25° C. for 30 min. Another portion of 10% palladium on activated carbon (100 mg) and triethylsilane (3 mL) was added and the mixture was stirred for 30 min. A third portion of 10% palladium on activated carbon (100 mg) and triethylsilane (3 mL) was added and the mixture was stirred for 30 min. The mixture was filtered to remove the catalyst and the solids washed with methanol. The filterate was concentrated in vacuo, azeotroped with toluene, dissolved in dichloromethane and concentrated in vacuo with silica gel (2 g). Purification by Biotage flash chromatography (Aspire 40 g column, 100% ethyl acetate) afforded (S)-2-amino-4,4-difluoro-pentanoic acid methyl ester (151 mg) as a clear colorless liquid.

Aufarbeitung

  1. customIn a flask under argon was placed
  2. stirringthe mixture was stirred for 30 min
  3. stirringthe mixture was stirred for 30 min
  4. filtrationThe mixture was filtered
  5. customto remove the catalyst
  6. washthe solids washed with methanol
  7. concentrationThe filterate was concentrated in vacuo
  8. customazeotroped with toluene
  9. dissolutiondissolved in dichloromethane
  10. concentrationconcentrated in vacuo with silica gel (2 g)
  11. customPurification by Biotage flash chromatography (Aspire 40 g column, 100% ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-a5f207c3c18646ceb932bfd46a4ee98e
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07741327B2

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