Hydrochloric Acid → Thieno[2,3-b]pyridine-2,3-diamine HCl salt

HRID 1615666Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1615666
[N+:1]([C:4]1[S:12][C:7]2=[N:8][CH:9]=[CH:10][CH:11]=[C:6]2[C:5]=1[NH2:13])([O-])=O.[ClH:14].CCOC(C)=O>CCO.[Ni]>[ClH:14].[S:12]1[C:7]2=[N:8][CH:9]=[CH:10][CH:11]=[C:6]2[C:5]([NH2:13])=[C:4]1[NH2:1]

Komponenten

6

Versuchsvorschrift

To a suspension of 2-nitrothieno[2,3-b]pyridin-3-amine (1.1 g, 5.6 mmol) in EtOH (60 mL) was added Raney Ni (1 g), followed by slow addition of N2H4.H2O (1.4 g, 22 mmol). The mixture was stirred at room temperature for 2 h. A solution of HCl in EtOAc (1 M, 18 mL, 18 mmol) was added to the reaction mixture slowly, and the mixture was filtered. The filter cake was washed with EtOAc (20 mL×3), then dried under reduced pressure to give the crude product as a yellow solid (2.7 g). ESI MS: m/z 166 [M+H]+.

Aufarbeitung

  1. filtrationthe mixture was filtered
  2. washThe filter cake was washed with EtOAc (20 mL×3)
  3. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9dc5937daf074e76b280e94996e42b11
Quelldatensatz
uspto-grants-2014_07
Patentnummer
US08765760B2

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