An efficient large??scale synthesis of 1H??indazole??[3??14C] carboxylic acid

RV Coelho, K Schildknegt

Index: Coelho Jr., Richard V.; Schildknegt, Klaas Journal of Labelled Compounds and Radiopharmaceuticals, 2007 , vol. 50, # 7 p. 675 - 678

Full Text: HTML

Citation Number: 2

Abstract

Abstract An efficient large-scale carbon-14 synthesis of 1H-indazole-[3-14 C] carboxylic acid starting from [14 C] potassium cyanide is reported. Key transformations encountered during the synthesis include aromatic nucleophilic substitution of 2-nitrofluorobenzene by ethyl [14 C] cyanoacetate, a mild decarbethoxylation and an aniline nitrosation/cyclization. Copyright© 2007 John Wiley & Sons, Ltd.

Related Articles:

Inactivation of monoamine oxidase B by benzyl 1-(aminomethyl) cyclopropane-1-carboxylate

[Silverman, Richard B.; Lu, Xingliang; Blomquist, Geri D.; Ding, Charles Z.; Yang, Shengtian Bioorganic and Medicinal Chemistry, 1997 , vol. 5, # 2 p. 297 - 304]

More Articles...