Reaktion #5936

ord-d606b4fe377c4554b35432c5e54a1380

Reaktionsgleichung

O=C(Cl)CCl
chloroacetyl chloride
Clc1ccc([C@@H]2CNc3ccccc3S2)cc1
(R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
CCN(CC)CC
triethylamine
O=C(CCl)N1C[C@@H](c2ccc(Cl)cc2)Sc2ccccc21
(R)-4-chloroacetyl-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine
Ausbeute 108.8%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISTILLATIONAfter the solvent is distilled off, to the residue
  2. 2
    workup.ADDITIONare added ethyl acetate and water
  3. 3
    Waschenthe ethyl acetate layer is washed with aqueous sodium hydrogen carbonate solution, water and saline
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    workup.DISTILLATIONdistilled
  6. 6
    Sonstigeto remove the solvent

Vorschrift

To a suspension of (R)-(+)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (1.30 g, 0.005 mole) and triethylamine (1.66 ml, 0.012 mole) in dichloromethane (16 ml) is added dropwise a solution of chloroacetyl chloride (0.79 ml, 0.01 mole) in dichloromethane (4 ml) under ice cooling, and the mixture is stirred at room temperature for 45 minutes. After the solvent is distilled off, to the residue are added ethyl acetate and water, and the ethyl acetate layer is washed with aqueous sodium hydrogen carbonate solution, water and saline, dried over sodium sulfate and distilled to remove the solvent to give (R)-4-chloroacetyl-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (1.84 g) as caramel.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246929uspto-grants-1993_09