87022-42-2Relevant articles and documents
Benzotriazol-1-ylalkyl Isocyanides: Versatile Synthons for Preparation of Unsymmetrical Formamidines
Katritzky, Alan R.,Sutharchanadevi, Murugan,Urogdi, Laszlo
, p. 1847 - 1851 (2007/10/02)
Adducts from benzotriazole, an aldehyde, and formamide are dehydrated to α-(benzotriazol-1-yl)alkyl isocyanides which readily add to secondary amines to form N'-(benzotriazol-1-ylalkyl)-N,N'-dialkylformamidines.The benzotriazolyl group in the latter is displaced by Grignard reagents to yield the corresponding unsymmetrical formamidines.
Synthesis of 1-Isocyanomethyl Azoles and Related Compounds
Saikachi, Haruo,Sasaki, Hideaki,Kitagawa, Tokujiro
, p. 723 - 726 (2007/10/02)
1-Isocyanomethyl azoles (11a-f) with trimethylformamidomethylammonium iodide (8), followed by dehydration of the resulting 1-formamidomethyl azoles (13a-f) using phosphorus oxychloride or triphenylphosphine/carbon tetrachloride.Furthermore, 1-substituted methyl-5-piperidinomethyltetrazoles(15a-f) were prepared by means of the four-component condensation of 14a-f with formaldehyde, sodium azide, and piperidine.Keywords - isocyanide; formamide; dehydration; azole; four-component condensation