Reaktion #41845

ord-1f25ff321e514b58b4c5fca27a5d1686

Reaktionsgleichung

O=S1(=O)CCCC1
sulfolane
c1ccc2c(N3CCNCC3)nsc2c1
3-piperazinylbenzo[d]isothiazole
O=C1Cc2cc(CCCl)c(Cl)cc2N1
6-chloro-5-(2-chloroethyl)indolin-2-one
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one
Ausbeute 74.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeIn glass-lined reactor placed
  2. 2
    TemperaturThe contents of the flask were initially heated to 75° C. to 80° C. for 2 hrs
  3. 3
    TemperaturThen temperature was raised to 95° C. to 100° C.
  4. 4
    workup.ADDITIONwas added to the reaction mixture
  5. 5
    workup.STIRRINGstirred
  6. 6
    FiltrationThe product was filtered off
  7. 7
    Waschenwashed with water
  8. 8
    Sonstigedried

Vorschrift

In glass-lined reactor placed 21.1 Kg (96.34 mole) of 3-piperazinylbenzo[d]isothiazole; 31 kg (134.7 moles) of 6-chloro-5-(2-chloroethyl)indolin-2-one; 1.1 kg of potassium iodide; 20.0 kg (111.92 mole) of potassium carbonate and 63.2 lit of sulfolane. The contents of the flask were initially heated to 75° C. to 80° C. for 2 hrs. Then temperature was raised to 95° C. to 100° C. and stirred till completion of the reaction. After completion of the reaction 210 lit of DM water was added to the reaction mixture and stirred. The product was filtered off and washed with water and dried to obtain 29.75 kg of 5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one (Ziprasidone).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728136B2uspto-grants-2010_06