24752-30-5Relevant articles and documents
A practical synthesis of 2-(N-substituted)-aminobenzimidazoles utilizing CuCl-promoted intramolecular cyclization of N-(2-aminoaryl)thioureas
Wang, Xiao-Jun,Zhang, Li,Xu, Yibo,Krishnamurthy, Dhileepkumar,Senanayake, Chris H.
, p. 7167 - 7170 (2004)
A practical protocol for synthesis of 2-(N-substituted)-aminobenzimidazoles was developed. N-(2-Aminoaryl)thioureas undergo a CuCl-promoted intramolecular cyclization to give the corresponding 2-(N-substituted amino)benzimidazoles in good to excellent isolated yields.
Ultrasound-assisted synthesis of substituted 2-aminobenzimidazoles, 2-aminobenzoxazoles, and related heterocycles
Phakhodee, Wong,Duangkamol, Chuthamat,Wiriya, Nittaya,Pattarawarapan, Mookda
, p. 5290 - 5293 (2016/11/11)
A sonochemical method for the synthesis of 2-aminobenzimidazoles and 2-aminobenzoxazoles, as well as chiral aminooxazolines and a chiral substituted quinazolin-5-one is reported. Using the Ph3P–I2system in the presence of triethylami
PROCESS FOR PREPARING 2-ARYLAMINO OR HETEROARYLAMINO SUBSTITUTED BENZIMIDAZOLE COMPOUNDS
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Page/Page column 9, (2011/02/24)
The present invention is related to a process for preparing 2-arylamino or heteroarylamino substituted benzimidazole compounds.