Reaktion #1755461

ord-4eac18d7e6fd4a71b9ac6f4d56a48bca

Reaktionsgleichung

Cc1cc(C)cc(CC(NS(=O)C(C)(C)C)c2cnn(C)c2)c1
2-methyl-propane-2-sulfinic acid [2-(3,5-dimethyl-phenyl)-1-(1-methyl-1H-pyrazol-4-yl)-ethyl]-amide
Cl
hydrogenchloride
Cc1cc(C)cc(CC(N)c2cnn(C)c2)c1
2-(3,5-Dimethyl-phenyl)-1-(1-methyl-1H-pyrazol-4-yl)-ethylamine
Ausbeute 77.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was quenched with aqueous potassium carbonate solution
  2. 2
    Extraktionextracted
  3. 3
    Trocknenthe organic phases dried over magnesium sulfate
  4. 4
    SonstigeAfter evaporation of the solvent a yellowish oil
  5. 5
    Sonstigewas obtained in 77% yield (1.05 g)

Vorschrift

A solution of RS 2-methyl-propane-2-sulfinic acid [2-(3,5-dimethyl-phenyl)-1-(1-methyl-1H-pyrazol-4-yl)-ethyl]-amide (2.0 g) in methanol (12 ml) was treated with a solution of hydrogenchloride in dioxane (12 ml, 4 N) at room temperature overnight. The reaction mixture was quenched with aqueous potassium carbonate solution and adjusted to pH 8-9, extracted and the organic phases dried over magnesium sulfate. After evaporation of the solvent a yellowish oil was obtained in 77% yield (1.05 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07989394B2uspto-grants-2011_08