تفاعل #640531

ord-57cb82a95d384ee4b75e6f8e4bb38f56

معادلة التفاعل

Nc1nonc1-c1nc2ccccc2n1CC(=O)c1ccc(Cl)c([N+](=O)[O-])c1
4-[1-(4-chloro-3-nitrophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine
Nc1cc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)ccc1Cl
title compound
Nc1cc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)ccc1Cl
4-[1-(3-Amino-4-chlorophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحFiltration and evaporation at reduced pressure
  2. 2
    أخرىgives the crude product
  3. 3
    أخرىPurification
  4. 4
    استخلاصby extraction with ethyl acetate and chromatography on silicagel

الإجراء التجريبي

To a stirred solution of 4-[1-(4-chloro-3-nitrophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine (0.07 g, 0.175 mmol) in ethanol (6 ml) and water (1 ml) is added two drops of concentrated hydrochloric acid and iron powder (0.1 g, 17.5 mmol). The reaction mixture is heated at 80° C. for 8 hours. Filtration and evaporation at reduced pressure gives the crude product. Purification by extraction with ethyl acetate and chromatography on silicagel yields the title compound as colorless solid, m.p. 228-230° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE042890E1uspto-grants-2011_11