반응 #2161258

ord-b71cabccb0344709a3929f93aa9aff49

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축The mixture is then concentrated
  2. 2
    추출extracted several times with dichloromethane
  3. 3
    건조The combined organic phases are dried over sodium sulfate
  4. 4
    농축concentrated
  5. 5
    기타dried in vacuo

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07919489B2uspto-grants-2011_04