Reaktion #41845
ord-1f25ff321e514b58b4c5fca27a5d1686
Reaktionsgleichung
sulfolane
3-piperazinylbenzo[d]isothiazole
6-chloro-5-(2-chloroethyl)indolin-2-one
potassium carbonate
→
5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one
Ausbeute 74.8%
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeIn glass-lined reactor placed
- 2TemperaturThe contents of the flask were initially heated to 75° C. to 80° C. for 2 hrs
- 3TemperaturThen temperature was raised to 95° C. to 100° C.
- 4workup.ADDITIONwas added to the reaction mixture
- 5workup.STIRRINGstirred
- 6FiltrationThe product was filtered off
- 7Waschenwashed with water
- 8Sonstigedried
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).