Ammonium formate → (S)-1-(3-(2-amino-5-methylphenoxy)piperidin-1-yl)-2,2,2-trifluoroethanone

HRID 240601Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 240601
C([O-])=O.[NH4+].[F:5][C:6]([F:27])([F:26])[C:7]([N:9]1[CH2:14][CH2:13][CH2:12][C@H:11]([O:15][C:16]2[CH:21]=[C:20]([CH3:22])[CH:19]=[CH:18][C:17]=2[N+:23]([O-])=O)[CH2:10]1)=[O:8]>[Pd].CO>[NH2:23][C:17]1[CH:18]=[CH:19][C:20]([CH3:22])=[CH:21][C:16]=1[O:15][C@H:11]1[CH2:12][CH2:13][CH2:14][N:9]([C:7](=[O:8])[C:6]([F:27])([F:5])[F:26])[CH2:10]1

Komponenten

5

Edukt 2

HCID 2723923Ammonium formateHCID 58413139(S)-2,2,2-trifluoro-1-(3-(5-methyl-2-nitrophenoxy)piperidin-1-yl)ethanone

Produkt 1

HCID 58413119(S)-1-(3-(2-amino-5-methylphenoxy)piperidin-1-yl)-2,2,2-trifluoroethanone

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 887MethanolLösungsmittel

Versuchsvorschrift

Amoniumformiate (0.238 g) was added into a suspension of (S)-2,2,2-trifluoro-1-(3-(5-methyl-2-nitrophenoxy)piperidin-1-yl)ethanone and palladium on charcoal (50.0 mg) in MeOH (6.0 ml) at room temperature. The mixture was heated at reflux for 40 mins. The mixture was filtered through a pad of celite and the filtercake was washed with dichloromethane. The filtrate was washed with water and. The residue was purfied by chromatography.

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 40 mins
  3. filtrationThe mixture was filtered through a pad of celite
  4. washthe filtercake was washed with dichloromethane
  5. washThe filtrate was washed with water

Quellen und Nachweise

ORD-Eintrag
ord-300843a7813441c6b1ca2abcb34f42f2
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08648068B2

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