Reaktion #5928

ord-5c1334df7ea540ff925a09322191a344

Reaktionsgleichung

C=CC(=O)Cl
acryloyl chloride
Clc1ccc(C2CNc3c(ccc4ccccc34)S2)cc1
3-(4-chlorophenyl)-2,3-dihydro1H-naphtho[2,1-b][1,4]thiazine
O=C([O-])O.[Na+]
sodium hydrogen carbonate
O
water
C=CC(=O)N1CC(c2ccc(Cl)cc2)Sc2ccc3ccccc3c21
3-(4-chlorophenyl)-1-propenoyl-2,3-dihydro-1H-naphtho[2,1-b][1,4]thiazine
Ausbeute 78.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONis added dropwise
  2. 2
    SonstigeThe organic layer is separated
  3. 3
    Waschenwashed
  4. 4
    Sonstigedried
  5. 5
    workup.DISTILLATIONdistilled
  6. 6
    Sonstigeto remove the solvent
  7. 7
    SonstigeThe residue is chromatographed on silica gel (toluene : acetone =50 : 1)

Vorschrift

To a mixture of 3-(4-chlorophenyl)-2,3-dihydro1H-naphtho[2,1-b][1,4]thiazine (1.50 g), sodium hydrogen carbonate (1.0 g), methylene chloride (30 ml) and water (15 ml) is added dropwise with stirring a solution of acryloyl chloride (0.90 g) in methylene chloride (10 ml) under ice cooling. The mixture is stirred at room temperature for 3 hours. The organic layer is separated, washed, dried and distilled to remove the solvent. The residue is chromatographed on silica gel (toluene : acetone =50 : 1) to give 3-(4-chlorophenyl)-1-propenoyl-2,3-dihydro-1H-naphtho[2,1-b][1,4]thiazine (1.37 g, 78 %) as powder.

Quelle

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