Preparation of 3-and 3, 5-substituted 1, 2, 4-triazoles

T Vaněk, V Velková, J Gut

Index: Vanek, Tomas; Velkova, Vlasta; Gut, Jiri Collection of Czechoslovak Chemical Communications, 1984 , vol. 49, # 11 p. 2492 - 2495

Full Text: HTML

Citation Number: 1

Abstract

Abstract Ethyl 1, 2, 4-triazole-3-carboxylate (V), its 5-methyl and 5-phenyl derivatives (V and VI, respectively), 3-methyl-1, 2, 4-triazole (VIII), 3-phenyl-1, 2, 4-triazole (IX), 3, 5-dimethy-1, 2, 4-triazole (X), 3, 5-diphenyl-1, 2, 4-triazole (XI) and 3-phenyl-5-methyl-1, 2, 4-triazole (XII) were prepared in 40-70% yields by thermal cyclization of acylamidrazones III.

Related Articles:

Thermal rearrangement of allyl substituted unsymmetric 4H-1, 2, 4-triazoles to the corresponding 1H-1, 2, 4-triazoles

[Jorgensen, Kare B.; Olsen, Ragnhild B.; Carlsen, Per H.J. Molecules, 2001 , vol. 6, # 5 p. 481 - 495]

Thermal rearrangement of allyl substituted unsymmetric 4H-1, 2, 4-triazoles to the corresponding 1H-1, 2, 4-triazoles

[Jorgensen, Kare B.; Olsen, Ragnhild B.; Carlsen, Per H.J. Molecules, 2001 , vol. 6, # 5 p. 481 - 495]

General??base catalysed hydrolysis and nucleophilic substitution of activated amides in aqueous solutions

[Buurma, Niklaas J.; Blandamer, Michael J.; Engberts, Jan B.F.N. Journal of Physical Organic Chemistry, 2003 , vol. 16, # 8 p. 438 - 449]

Triazoles. Part III. Mono-and di-methyl (phenyl)-1: 2: 4-triazoles

[Atkinson; Polya Journal of the Chemical Society, 1954 , p. 3319,3322]

More Articles...