药学研究
藥學研究
약학연구
JOURNAL OF PHARMACEUTICAL RESEARCH
2015年
1期
57-58
,共2页
阿苯达唑%4-丙硫基邻苯二胺%合成
阿苯達唑%4-丙硫基鄰苯二胺%閤成
아분체서%4-병류기린분이알%합성
Albendazole%4-propylthio pheylenediamine%Synthesis
目的：制备4—丙硫基邻苯二胺。方法采用镍铝合金—氯化铵还原体系，还原4—丙硫基—2—硝基苯胺制备4—丙硫基邻苯二胺。结果及结论4—丙硫基邻苯二胺的收率达到90%以上，具有较好的应用前景。
目的：製備4—丙硫基鄰苯二胺。方法採用鎳鋁閤金—氯化銨還原體繫，還原4—丙硫基—2—硝基苯胺製備4—丙硫基鄰苯二胺。結果及結論4—丙硫基鄰苯二胺的收率達到90%以上，具有較好的應用前景。
목적：제비4—병류기린분이알。방법채용얼려합금—록화안환원체계，환원4—병류기—2—초기분알제비4—병류기린분이알。결과급결론4—병류기린분이알적수솔체도90%이상，구유교호적응용전경。
Pbjective To prepare 4—propylthio pheylenediamine. Methods The 4—propylthio pheylenediamine was synthesized through reduction of 4—propylthio—2—nitro aniline with nickel aluminium alloy—ammonium chloride as re-ductant. ResuIts and ConcIusion The target compound was obtained in the yield of 90% above. The procedure′s applica-tion prospect was broad.
