3070-87-9Relevant articles and documents
Preparation method 3,3 '-dinitro -4, 4' - diacetyl diaminodiphenyl ether
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Paragraph 0069; 0071-0073; 0075-0077; 0079-0081; 0084; ..., (2021/09/26)
The preparation method of 3, 3 ’ -dinitro -4 and 4 ’ -diacetyl diaminodiphenyl ether comprises the following steps of: adding an acylating agent to 4 and 4 ’ - diaminodiphenyl ether to carry out acylation reaction to obtain an acylation product. The nitra
Newly synthesized bis-benzimidazole derivatives exerting anti-tumor activity through induction of apoptosis and autophagy
Wang, Xiu-Jun,Chu, Na-Ying,Wang, Qin-He,Liu, Chao,Jiang, Chun-Guo,Wang, Xiao-Yu,Ikejima, Takashi,Cheng, Mao-Sheng
supporting information, p. 6297 - 6300 (2012/11/06)
In this study, a new series of bis-benzimidazole derivatives were designed and synthesized. Most of these new compounds showed significant anti-tumor activity in vitro compared to Hoechst 33258. Among them, the most potent compound 8 had the IC50/su
Synthesis and structure of Di[methoxy(ethoxy)carbonylamino-1H-benzimidazol- 5-yl] ethers
Pilyugin,Sapozhnikov,Kiseleva,Sapozhnikova,Vorob'eva,Klimakova
, p. 1509 - 1513 (2007/10/03)
A procedure was developed for preparing di[methoxy(ethoxy)carbonylamino-1H- benzimidazol-5-yl] ethers by the reaction of methyl or ethyl chloroformate with sodium cyanamide, followed by the reaction of the resulting methyl or ethyl cyanocarbamate with 4-(3,4-diaminophenoxy)-1,2-phenylenediamine in acidic solution. 2005 Pleiades Publishing, Inc.