Hydroxylamine → (S)-2-((R)-2-(4-Fluoro-3-methylphenyl)-2-methoxyethyl)-N-hydroxypent-4-enamide

HRID 1643284Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1643284
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([O:18][CH3:19])[CH2:9][C@H:10]([CH2:15][CH:16]=[CH2:17])[C:11](OC)=[O:12])=[CH:4][C:3]=1[CH3:20].C1COCC1.[NH2:26][OH:27].[C-]#N.[K+]>O.CO>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([O:18][CH3:19])[CH2:9][C@H:10]([CH2:15][CH:16]=[CH2:17])[C:11]([NH:26][OH:27])=[O:12])=[CH:4][C:3]=1[CH3:20]

Komponenten

7

Versuchsvorschrift

(S)-Methyl 2-((R)-2-(4-fluoro-3-methylphenyl)-2-methoxyethyl)pent-4-enoate (50 mg) was dissolved into 1 mL of a mixture of THF, methanol, and 50% NH2OH in H2O (2:2:1) and to this solution was added 2 mg KCN. The reaction was stirred for 3 days at room temperature and then quenched by the addition of 1M HCl (10 mL). The mixture was extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with brine (2×10 mL) before being concentrated under reduced pressure. The product was isolated by flash column chromatography eluting with 0% to 10% methanol/DCM to obtain the title compound (34 mg) as white solid.

Aufarbeitung

  1. customquenched by the addition of 1M HCl (10 mL)
  2. extractionThe mixture was extracted with ethyl acetate (3×20 mL)
  3. washThe combined organic layers were washed with brine (2×10 mL)
  4. concentrationbefore being concentrated under reduced pressure
  5. customThe product was isolated by flash column chromatography
  6. washeluting with 0% to 10% methanol/DCM

Quellen und Nachweise

ORD-Eintrag
ord-4696ee3eb0d7433dacfa4d627db1b57b
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08119692B2

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