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Hydrochloric Acid → (3S,5S,6R)-3-amino-5-(2-fluoro-3-methylphenyl)-6-methyl-1-(2,2,2-trifluoroethyl)piperidin-2-one

HRID 448216
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 448216
[F:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[C:9]1[CH:10]=[C:11]([N+:22]([O-])=O)[C:12](=[O:21])[N:13]([CH2:16][C:17]([F:20])([F:19])[F:18])[C:14]=1[CH3:15].Cl.[H][H]>CO.[Pt](=O)=O>[NH2:22][C@H:11]1[CH2:10][C@@H:9]([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([CH3:8])[C:2]=2[F:1])[C@@H:14]([CH3:15])[N:13]([CH2:16][C:17]([F:19])([F:18])[F:20])[C:12]1=[O:21]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 86665195HCID 86665195, VerbindungHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 68748739(3S,5S,6R)-3-amino-5-(2-fluoro-3-methylphenyl)-6-methyl-1-(2,2,2-trifluoroethyl)piperidin-2-one

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 345198Adams' catalystKatalysator
HCID 887
Methanol
Lösungsmittel

Versuchsvorschrift

A mixture of 5-(2-fluoro-3-methylphenyl)-6-methyl-3-nitro-1-(2,2,2-trifluoroethyl)pyridin-2(1H)-one (1.95 g, 5.66 mmol), platinum(IV) oxide (0.643 g, 2.83 mmol), and concentrated aqueous hydrochloric acid solution (12 M, 4.72 mL, 56.6 mmol) in methanol (57 mL) was shaken under 50 psi of hydrogen at 23° C. for 5 h. The catalyst was removed by filtration through Celite® and washed thoroughly with methanol. The filtrate was concentrated, and the residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic layer was washed with brine, dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography on silica gel, eluting with dichloromethane initially, grading to 5% MeOH (basified 0.1% concentrated aqueous ammonium hydroxide solution) in dichloromethane to give the title compound as a racemate. The enantiomers were separated by normal-phase HPLC using a ChiralCel® OD column, eluting with 40% hexane in ethanol (0.1% diethylamine used as a modifier) to afford the title compound as the second enantiomer to elute. MS: m/z=319.2 (M+1).

Aufarbeitung

  1. customThe catalyst was removed by filtration through Celite®
  2. washwashed thoroughly with methanol
  3. concentrationThe filtrate was concentrated
  4. customthe residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution
  5. washThe organic layer was washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated
  8. customThe residue was purified by flash column chromatography on silica gel
  9. washeluting with dichloromethane initially

Quellen und Nachweise

ORD-Eintrag
ord-224dc2879f3e4a5f8318f715f9b919be
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08481556B2

Notizen zur Reaktion

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