Reaktion #171307

ord-86209a96cdaa42ce870321d1ddeafa0e

Reaktionsgleichung

O
water
CC1CN(C(=O)C(F)(F)F)CCc2ccc(Cl)cc21
N-trifluoroacetyl-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
F[B-](F)(F)F.F[B-](F)(F)F.F[N+]12CC[N+](CCl)(CC1)CC2
Selectfluor
O=S(=O)(O)C(F)(F)F
trifluoromethanesulfonic acid
CC1CN(C(=O)C(F)(F)F)CCc2cc(F)c(Cl)cc21
white solid
Ausbeute 60.8%
CC1CN(C(=O)C(F)(F)F)CCc2cc(F)c(Cl)cc21
N-Trifluoroacetyl-8-chloro-7-fluoro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine
Ausbeute 60.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with EtOAc (200 mL)
  2. 2
    Waschenthe organic phase washed with saturated aqueous NaHCO3 (2×100 mL), brine (100 mL)
  3. 3
    Trocknendried with Na2SO4
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe crude product was purified by flash chromatography (6% EtOAc in hexane, silica)

Vorschrift

A solution of N-trifluoroacetyl-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (2.5 g, 8.5 mmol) in 1,2-dichloroethane (15 mL) was treated with Selectfluor (3.9 g, 11 mmol), trifluoromethanesulfonic acid (8 mL, 90 mmol) and stirred 60 hours at 75 C. The product mixture was poured into water (200 mL), extracted with EtOAc (200 mL), the organic phase washed with saturated aqueous NaHCO3 (2×100 mL), brine (100 mL), dried with Na2SO4 and concentrated. The crude product was purified by flash chromatography (6% EtOAc in hexane, silica) resulting in 1.6 g of a white solid. MS calculated for C13H12ClF4NO+H: 310, observed: 310.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846906B2uspto-grants-2014_09