Reaktion #4724

ord-e24ed27fe652417993abf3a0ffe56ba7

Reaktionsgleichung

OO
Hydrogen peroxide
CNC(=S)NNC(=S)NCCCOc1cccc(CN2CCCCC2)c1
N-methyl-N'-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-1,2-hydrazine dicarbothioamide
CNc1nnc(NCCCOc2cccc(CN3CCCCC3)c2)s1
N-Methyl-N'-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]1,3,4-thiadiazole-2,5-diamine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture is briefly heated to boiling
  2. 2
    FiltrationThe sulphur which separates is filtered off hot with the aid of active charcoal
  3. 3
    Einengenthe filtrate is concentrated by evaporation
  4. 4
    Sonstigepurified by preparative layer chromatography

Vorschrift

2 ml of 30% Hydrogen peroxide are added to 1.58 g (4 mmol) of N-methyl-N'-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-1,2-hydrazine dicarbothioamide in 30 ml of ethanol and the reaction mixture is briefly heated to boiling. The sulphur which separates is filtered off hot with the aid of active charcoal and the filtrate is concentrated by evaporation and purified by preparative layer chromatography.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04727081uspto-grants-1988_02