1010691-00-5Relevant articles and documents
A practical, metal-free synthesis of 1H-Lndazoles
Counceller, Carla M.,Eichman, Chad C.,Wray, Brertda C.,Stambuli, James P.
supporting information; experimental part, p. 1021 - 1023 (2009/04/07)
The synthesis of 1H-indazoles is achieved from o-aminobenzoximes by the selective activation of the oxime in the presence of the amino group. The reaction occurs with a variety of substituted o-aminobenzoximes using a slight excess of methanesulfonyl chloride and triethylamine at 0-23 °C and is amenable to scale-up. The synthesis of 1 H-indazoles under these conditions is extremely mild compared with previous synthetic approaches and affords the desired compounds in good to excellent yields.
