Stannous chloride dihydrate → 2-Amino-N-quinolin-8-yl-benzenesulfonamide

HRID 513545Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 513545
O.O.[Sn](Cl)Cl.[N+:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[S:15]([NH:18][C:19]1[CH:20]=[CH:21][CH:22]=[C:23]2[C:28]=1[N:27]=[CH:26][CH:25]=[CH:24]2)(=[O:17])=[O:16])([O-])=O>CCO>[NH2:6][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[S:15]([NH:18][C:19]1[CH:20]=[CH:21][CH:22]=[C:23]2[C:28]=1[N:27]=[CH:26][CH:25]=[CH:24]2)(=[O:17])=[O:16]

Komponenten

4

Versuchsvorschrift

Tin (II) chloride dihydrate (4.11 g, 18.2 mmol) was added to a solution of 2-nitro-N-quinolin-8-yl-benzenesulfonamide (Example Compound 6) (2.0 g, 6.07 mmol) in EtOH (50 ml) and the mixture was heated under reflux for 2 h. After cooling, the mixture was concentrated in vacuo. The crude residue was dissolved in EtOAc (40 ml) and cooled in an ice bath, the mixture was basified with aqueous ammonia. The resulting white precipitate was collected by filtration, washed with EtOAc and discarded. The organic combined organic filtrates were washed with brine, dried (Na2SO4) and concentrated in vacuo to give the title compound (1.82 g, 53%).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 2 h
  3. temperatureAfter cooling
  4. concentrationthe mixture was concentrated in vacuo
  5. dissolutionThe crude residue was dissolved in EtOAc (40 ml)
  6. temperaturecooled in an ice bath
  7. filtrationThe resulting white precipitate was collected by filtration
  8. washwashed with EtOAc
  9. washThe organic combined organic filtrates were washed with brine
  10. dry with materialdried (Na2SO4)
  11. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-a3b0524498184d1fac8cfc3fb199a40a
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09102688B2

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