187083-45-0Relevant articles and documents
Microwave enhanced reduction of nitro and azido arenes to N-arylformamides employing Zn-HCOONH4: Synthesis of 4(3H)-quinazolinones and pyrrolo[2,1-c][1,4]benzodiazepines
Kamal, Ahmed,Srinivasa Reddy,Rajendra Prasad,Hari Babu,Ramana, A. Venkata
, p. 6517 - 6521 (2004)
Microwave mediated reduction of nitro and azido arenes to N-arylformamides using Zn-HCOONH4 is described. In the absence of microwave conditions, this methodology affords amines. This protocol has been extended to the synthesis of pyrrolo[2,1-c][1,4]benzodiazepines and 4(3H)-quinazolinones.
The Synthesis of Functionalized Pyrrolo-[2,1-c][1,4]-Benzodiazepines
O'Neil, Ian A.,Murray, Clare L.,Hunter, Rachel C.,Kalindjian, S. Barret,Jenkins, Terry C.
, p. 75 - 78 (2007/10/03)
Two concise and high yielding routes to the antitumour antibiotic pyrrolo-[2,1-c][1,4]-benzodiazepine ring system are described. Thus, condensation of prolinol with 2-azidobenzoylchloride gives the tertiary amide (3). Oxidation to the aldehyde (4) followe