تفاعل #2045113

ord-e3d56b6de5994fb9962cfd1f4d0c6f16

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture is then concentrated
  2. 2
    استخلاصextracted repeatedly with dichloromethane
  3. 3
    تجفيفThe combined organic phases are dried over sodium sulphate
  4. 4
    تركيزconcentrated
  5. 5
    أخرىdried under reduced pressure

الإجراء التجريبي

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 made alkaline using 1M aqueous sodium hydroxide solution and extracted repeatedly with dichloromethane. The combined organic phases are dried over sodium sulphate, concentrated and dried under reduced pressure.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08410090B2uspto-grants-2013_04