Reaction #2161258

ord-b71cabccb0344709a3929f93aa9aff49

Reaction equation

Cc1ccc(N2CCN(C(=O)OC(C)(C)C)CC2)nc1
1-(tert-butyloxycarbonyl)-4-(5-methylpyridin-2-yl)piperazine
Cl
hydrogen chloride
Cc1ccc(N2CCNCC2)nc1
1-(5-Methylpyridin-2-yl)piperazine

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    ConcentrationThe mixture is then concentrated
  2. 2
    Extractionextracted several times with dichloromethane
  3. 3
    DryingThe combined organic phases are dried over sodium sulfate
  4. 4
    Concentrationconcentrated
  5. 5
    Otherdried in vacuo

Procedure

3.47 g (12.5 mmol) of 1-(tert-butyloxycarbonyl)-4-(5-methylpyridin-2-yl)piperazine are dissolved in 10 ml of dioxane, and 31 ml (125 mmol) of hydrogen chloride in dioxane (4 molar) are added. The mixture is stirred at RT for 2 h. The mixture is then concentrated and the residue is rendered alkaline using a 1M aqueous sodium hydroxide solution and extracted several times with dichloromethane. The combined organic phases are dried over sodium sulfate, concentrated and dried in vacuo.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07919489B2uspto-grants-2011_04