Reaktion #3251

Reaktionsgleichung

6-chloro-3-fluoro-7H-indeno[2,1-c]quinoline-7-on

N,N-dimethylethylenediamine

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title compound

Ausbeute 68.6%

6-(((dimethylamino)ethyl)amino)-3-fluoro-7H-indeno[2,1-c]quinoline-7-on dihydrochloride

Ausbeute 68.6%

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.DISTILLATIONThe reaction mixture was distilled to dryness
2. 2
   workup.ADDITIONTo the residue was added water and chloroform
3. 3
   Extraktionfor extraction
4. 4
   TrocknenThe chloroform layer was dried over magnesium sulfate
5. 5
   Sonstigeevaporated
6. 6
   SonstigeThe residue was purified by silica gel column chromatography (eluent; chloroform:ethanol=10:1(v/v))
7. 7
   workup.DISSOLUTIONThe purified material was dissolved in 20 ml of tetrahydrofuran
8. 8
   workup.ADDITIONTo the the solution was added 4N-hydrochloride/dioxane (2 ml)
9. 9
   Einengenthe mixture was concentrated under reduced pressure
10. 10
    SonstigeThe residue obtained
11. 11
    Sonstigewas crystallized from diethylether

Vorschrift

To a suspension of 6-chloro-3-fluoro-7H-indeno[2,1-c]quinoline-7-on (860 mg, 3.0 mmol) in pyrydine (10 ml) was added N,N-dimethylethylenediamine (800 mg, 9.0 mmol), and the mixture was stirred with heat at 90° C. for 12 hours. The reaction mixture was distilled to dryness. To the residue was added water and chloroform for extraction. The chloroform layer was dried over magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (eluent; chloroform:ethanol=10:1(v/v)). The purified material was dissolved in 20 ml of tetrahydrofuran. To the the solution was added 4N-hydrochloride/dioxane (2 ml) and the mixture was concentrated under reduced pressure. The residue obtained was crystallized from diethylether to give 420 mg (yield 34.3%) of title compound. The physicochemical properties thereof are shown in table 1.

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