Reaktion #305316

ord-e1a142618bcf4bfaa529b9d80e7bc35f

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe mixture was carefully quenched with MeOH
  2. 2
    workup.ADDITIONpoured into brine
  3. 3
    Extraktionextracted with ethyl acetate (2×100 mL)
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Einengenconcentrated

Vorschrift

(a)(b) To a stirred solution of (S)-2,2-dimethyl-3-(1-methyl-1H-indazol-5-yl)-3-phenylpropanenitrile (24 mg, 0.078 mmol) in anhydrous THF (10 mL) was added 1.0M lithium aluminum hydride in diethyl ether (0.5 mL, 0.5 mmol) portionwise at RT under nitrogen. After stirring at RT for 3 hr, the mixture was carefully quenched with MeOH, poured into brine, extracted with ethyl acetate (2×100 mL), dried (MgSO4) and concentrated. The crude product was coupled with 2,2,2-trifluoroethanesulfonyl chloride (14 mg, 0.073 mmol) using General Coupling Method B to give (S)—N-(2,2-dimethyl-3-(1-methyl-1H-indazol-5-yl)-3-phenylpropyl)-3,3,3-trifluoropropanamide. MS found: (M+H)+=468.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08198311B2uspto-grants-2012_06