Reaction #4705

ord-fc8d952f1485405099b4c829a6ef36c1

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.WAITthe reaction mixture is left
  2. 2
    Otherthe precipitation
  3. 3
    Filtrationfiltered
  4. 4
    Washwashed with ether
  5. 5
    Otherrecrystallised from ethanol

Procedure

1.62 g (5 mmol) of N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]hydrazine carbothioamide are dissolved in 30 ml of THF, 0.40 g (6 mmol) of methylisocyanate are added and the reaction mixture is left to stand overnight at room temperature. Ether is added to complete the precipitation, and the precipitate is suction filtered, washed with ether and recrystallised from ethanol. The analytical values are summarized in Table I.

Source

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