Reaktion #50007

Reaktionsgleichung

bromine

2,4-dichloro-6-fluoro-7-isothiocyanatobenzothiazole

2-amino-4,4-dimethylpyrroline hydrochloride

sodium hydroxide

→

2,4-Dichloro-7-(6,6-dimethyl-3,5,6,7-tetrahydropyrrolo-[2,1-c][1,2,4]thiadiazol-3-ylidenamino)-6-fluorobenzothiazole

Lösungsmittel

dichloromethane

dichloromethane

dichloromethane

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigerose to 20° C
2. 2
   TemperaturThe mixture was cooled to -10° C.
3. 3
   workup.STIRRINGdropwise, slowly and the mixture stirred for I hour whereby the temperature
4. 4
   Sonstigerose to 10° C
5. 5
   WaschenThe solution was washed with water and with dilute caustic soda
6. 6
   Trocknendried over magnesium sulfate
7. 7
   Einengenconcentrated
8. 8
   SonstigeThe residue was recrystallised from diisopropyl ether

Vorschrift

A solution of 2 g 2,4-dichloro-6-fluoro-7-isothiocyanatobenzothiazole in 10 ml dichloromethane was added, dropwise, at 0° C., to a suspension of 1.1 g 2-amino-4,4-dimethylpyrroline hydrochloride in 20 ml dichloromethane. A solution of 0.3 g sodium hydroxide and 6 ml water was added, dropwise, at 2° C. to this mixture which was stirred for 3 hours, whereby the temperature rose to 20° C. The mixture was cooled to -10° C. and a solution of 1 g bromine in 10 ml dichloromethane was added, dropwise, slowly and the mixture stirred for I hour whereby the temperature rose to 10° C. The solution was washed with water and with dilute caustic soda, dried over magnesium sulfate and concentrated. The residue was recrystallised from diisopropyl ether. Yield: 1.5 g=53% of theory m.p.: 134°-136° C.

Quelle