Reaktion #1787806

Reaktionsgleichung

7-(2-chlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one

1-amino-3-hydroxyguanidine p-toluenesulfonate

hydrochloric acid

→

7-(2-chlorophenyl)-5-(1-hydroxyguanidin-3-yl)imino-4-methyl-5,6,7,8-tetrahydroquinoline hydrochloride

Ausbeute 166.3%

Lösungsmittel

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe reaction solution was concentrated under reduced pressure
2. 2
   workup.ADDITIONto the residue were added ethyl acetate (40 ml), tetrahydrofuran (30 ml) and 0.2 N sodium hydroxide (50 ml)
3. 3
   workup.STIRRINGThe mixture was shaken
4. 4
   Waschenthe separated upper layer was washed with 0.2 N sodium hydroxide (20 ml) and water (15 ml, thrice)
5. 5
   workup.ADDITIONTo the upper layer was added 2 N hydrochloric acid (2.5 ml)
6. 6
   Einengenthe mixture was concentrated under reduced pressure
7. 7
   workup.ADDITIONTo the residue was added ethanol (10 ml)
8. 8
   workup.STIRRINGthe mixture was stirred at 900° C. (bath temperature) for 3 hours
9. 9
   Temperaturcooled
10. 10
    Sonstigeto give crystals, which
11. 11
    Filtrationwere filtered

Vorschrift

A mixture of 7-(2-chlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one (679 mg), 1-amino-3-hydroxyguanidine p-toluenesulfonate (917 mg) and concentrated hydrochloric acid (0.3 ml) in ethanol (10 ml) was stirred at 90° C. (bath temperature) for 3 hours. The reaction solution was concentrated under reduced pressure, and to the residue were added ethyl acetate (40 ml), tetrahydrofuran (30 ml) and 0.2 N sodium hydroxide (50 ml). The mixture was shaken, and the separated upper layer was washed with 0.2 N sodium hydroxide (20 ml) and water (15 ml, thrice). To the upper layer was added 2 N hydrochloric acid (2.5 ml), and the mixture was concentrated under reduced pressure. To the residue was added ethanol (10 ml), and the mixture was stirred at 900° C. (bath temperature) for 3 hours and cooled to give crystals, which were filtered to give 7-(2-chlorophenyl)-5-(1-hydroxyguanidin-3-yl)imino-4-methyl-5,6,7,8-tetrahydroquinoline hydrochloride (Compound 106) (790 mg) as pale yellow crystals.

Quelle