67119-49-7Relevant articles and documents
Rapid reduction of heteroaromatic nitro groups using catalytic transfer hydrogenation with microwave heating
Quinn, John F.,Bryant, Cole E.,Golden, Kathryn C.,Gregg, Brian T.
scheme or table, p. 786 - 789 (2010/03/24)
A method for the rapid, safe reduction of heteroaromatic and aromatic nitro groups to amines is described using catalytic transfer hydrogenation under microwave heating conditions. Commonly available Pd/C or Pt/C catalyst is extremely effective with 1,4-cyclohexadiene as the hydrogen transfer source. In the case of substrates containing potentially labile aromatic halogens, Pt/C is effective and results in little or no dehalogenation. In general, the reactions are complete within 5 min at 120 °C.
A convenient sonochemical synthesis of vicinally substituted 3-hydroxylaminopyridines
Rusinov, G. L.,Filatov, I. E.,Pashkevich, K. I.
, p. 325 - 327 (2007/10/02)
A method of synthesis of vicinally substituted N-(3-pyridyl)hydroxylamines by reducing the corresponding nitropyridines with Zn/NH4Cl/EtOH under ultrasonication is proposed.Ultrasound irradiation increases the yields of these hydroxylamines and facilitates their isolation.