تفاعل #1810809

ord-9b19962bafd74275a9dbc508e2813d53

معادلة التفاعل

CN=C(SC)N(C)C1CCC(NC(=O)OCc2ccccc2)CC1
[4-(1,2,3-trimethyl-isothioureido)-cyclohexyl]carbamic acid benzylester
I
hydroiodide
[Cl-]
chloride
CCO
EtOH
NN.O
hydrazine monohydrate
CN=C(NN)N(C)C1CCC(NC(=O)OCc2ccccc2)CC1
[4-(3-Amino-1,2-dimethyl-guanidino)-cyclohexyl]-carbamic acid benzylester
Cl
hydrochloride

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA suspension obtained
  2. 2
    ترشيحis filtered
  3. 3
    أخرىthe filtrate obtained
  4. 4
    أخرىThe mixture obtained
  5. 5
    درجة الحرارةis refluxed for 2.5 hours and from the mixture
  6. 6
    أخرىobtained solvent
  7. 7
    أخرىis evaporated

الإجراء التجريبي

0.84 g of [4-(1,2,3-trimethyl-isothioureido)-cyclohexyl]carbamic acid benzylester in the form of a hydroiodide are stirred with 10 ml of of a strong basic ion exchanger in chloride form. A suspension obtained is filtered and the filtrate obtained is lyophilized. The lyophilisate is treated with 15 ml of EtOH and with 0.08 ml of hydrazine monohydrate. The mixture obtained is refluxed for 2.5 hours and from the mixture obtained solvent is evaporated. [4-(3-Amino-1,2-dimethyl-guanidino)-cyclohexyl]-carbamic acid benzylester in the form of a hydrochloride is obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07485632B2uspto-grants-2009_02