Hydrochloric Acid → 5-(5-Isoquinolylsulfanyl)isoquinoline
Reaktionsgleichung
Cl.N[C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][N:7]=[CH:8]2.[N-]=[N+]=[N-].[Na+].C([O-])(=O)C.[Na+].[OH-].[Na+].[CH:24]1[C:33]2[CH:32]=[CH:31][CH:30]=[C:29]([SH:34])[C:28]=2[CH:27]=[CH:26][N:25]=1>C(OCC)(=O)C.O>[CH:8]1[C:9]2[C:4](=[C:3]([S:34][C:29]3[CH:30]=[CH:31][CH:32]=[C:33]4[C:28]=3[CH:27]=[CH:26][N:25]=[CH:24]4)[CH:12]=[CH:11][CH:10]=2)[CH:5]=[CH:6][N:7]=1Komponenten
Edukt 6
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To an aqueous 4N hydrochloric acid solution 24 ml of 5-aminoisoquinoline 1.00 g (6.9 mmol), a water solution 2 ml of sodium azide 480 mg (6.9 mmol) was added dropwise. The reaction mixture was stirred at 0° C. for 30 minutes and neutralized with sodium acetate, and insoluble materials were filtered. The filtrate was added to a sodium hydroxide solution (300 mg/3 ml) of 5-isoquinolinethiol 1.23 g (7.6 mmol), and the mixture was stirred for 1.5 hours at 80° C. After adding ethyl acetate, the reaction solution was washed with 1N sodium hydroxide and saturated sodium chloride, and dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure, the resulting residue was purified by silica gel column chromatography (ethyl acetate), and 5-(5-isoquinolylsulfanyl)isoquinoline 230 mg (11.5%) was obtained.
Aufarbeitung
- filtrationwere filtered
- stirringthe mixture was stirred for 1.5 hours at 80° C
- washthe reaction solution was washed with 1N sodium hydroxide and saturated sodium chloride
- dry with materialdried over anhydrous magnesium sulfate
- concentrationThe organic layer was concentrated under reduced pressure
- customthe resulting residue was purified by silica gel column chromatography (ethyl acetate)
Quellen und Nachweise
- ORD-Eintrag
- ord-e91e54707b5f44f1aa3b1a0c322e892f
- Quelldatensatz
- uspto-grants-1999_09
- Patentnummer
- US05959107
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