Reaktion #169063

Reaktionsgleichung

triethylamine

2,4-dichloro-3-nitroquinoline

1,2-diamino-2-methylpropane

→

N1-(2-chloro-3-nitroquinolin-4-yl)-2-methylpropane-1,2-diamine

Ausbeute 99.9%

Lösungsmittel

1-methyl-2-pyrrolidinone

1-methyl-2-pyrrolidinone

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwhile maintaining the temperature of the reaction mixture below 4° C
2. 2
   workup.ADDITIONAfter the addition
3. 3
   Sonstigewas removed
4. 4
   workup.ADDITIONThe reaction mixture was slowly poured
5. 5
   workup.STIRRINGinto vigorously stirred
6. 6
   Temperaturwarm water (300 mL)
7. 7
   workup.STIRRINGThe resulting suspension was stirred for 1 hour
8. 8
   Temperaturcooled to 13° C.
9. 9
   workup.ADDITIONby adding ice
10. 10
    SonstigeThe solid was isolated by filtration
11. 11
    Waschenwashed with cold water until the filtrate

Vorschrift

Under a nitrogen atmosphere, triethylamine (6.6 mL, 47 mmol) was added slowly to a solution of 2,4-dichloro-3-nitroquinoline (10.0 g, 41.1 mmol) in anhydrous 1-methyl-2-pyrrolidinone (40 mL). The reaction mixture was cooled to 0° C. with an ice bath. A solution of 1,2-diamino-2-methylpropane (4.1 g, 47.3 mmol) in anhydrous 1-methyl-2-pyrrolidinone (5 mL) was added dropwise over a period of 15 minutes while maintaining the temperature of the reaction mixture below 4° C. After the addition was completed the ice bath was removed and the reaction mixture was allowed to stir at ambient temperature for 4 hours. The reaction mixture was slowly poured into vigorously stirred warm water (300 mL). The resulting suspension was stirred for 1 hour and then cooled to 13° C. by adding ice. The solid was isolated by filtration and then washed with cold water until the filtrate was clear to provide 12.1 g of N1-(2-chloro-3-nitroquinolin-4-yl)-2-methylpropane-1,2-diamine as a damp yellow solid.

Quelle