34776-19-7

Usage

Uses

Used in Pharmaceutical Industry:
1,5-DIMETHYL-1H-[1,2,4]TRIAZOL-3-YLAMINE is used as a building block for the development of new drugs in medicinal chemistry. Its unique structure and properties make it a valuable component in the creation of innovative pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In agricultural chemistry, 1,5-DIMETHYL-1H-[1,2,4]TRIAZOL-3-YLAMINE serves as a precursor for the synthesis of various pesticides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and diseases, thereby contributing to improved crop yields and food security.
Used in Scientific Research:
1,5-DIMETHYL-1H-[1,2,4]TRIAZOL-3-YLAMINE is also employed as a reagent or intermediate in chemical reactions within scientific research. Its presence in various reaction schemes allows researchers to explore new chemical pathways and synthesize novel compounds for further study and potential applications.

InChI:InChI=1/C4H8N4/c1-3-6-4(5)7-8(3)2/h1-2H3,(H2,5,7)

Upstream product

• 60-34-4 methylhydrazine 

Downstream Products

• 1225444-48-3 5-(1,5-dimethyl-1H-[1,2,4]triazol-3-ylamino)-2-(4-methyl-imidazol-1-yl)-benzonitrile 

Relevant academic research and scientific papers

Process for producing sulfonylureas

There is described a novel process for producing sulfonylureas of formula I STR1 wherein R1 is hydrogen or alkyl, R2 is STR2 E is =N-- or =CH--, R3 is alkyl, alkoxy or halogen, R4 is alkyl, cycloalkyl, alkoxy, halogen, alkoxy-alkyl, halo-alkyl or halo-alkoxy, R5 is hydrogen or alkyl, T is a substituted phenyl group STR3 Y is hydrogen or halogen, X is hydrogen, halogen, alkyl, halo-alkyl, alkenyl, halo-alkenyl, alkynyl, alkoxy, halo-alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, halo-alkylthio, alkylsulfonyloxy, phenylsulfonyloxy, phenylsulfonyloxy mono- or polysubstituted by alkyl, or is di-alkylsulfamoyl, and A is a bridge member which has 3 or 4 atoms and which contains 1 or 2 hetero atoms, selected from the group consisting of oxygen, sulfur and nitrogen, the said process comprising reacting a silfonamide of the formula II in the presence of a base, with diphenyl carbonate to form a salt of a phenyl carbamate converting this salt into the free phenyl carbamate and reacting this further with an amine. Sulfonylureas are herbicidally effective compounds.

113. Notiz ueber die Reaktion von Methylhydrazin mit N-Cyano-azomethinen. Abhaengigkeit des Reaktionsverlaufs von der Natur der Abgangsgruppe

The reaction of methylhydrazine with N-cyanoazomethines 1 containing a thioalkyl leaving group yields the 3-amino-1,2,4-triazole derivatives 2, whereas the N-cyanoazomethines 1 containing an alkoxy leaving group give the isomeric 5-amino-1,2,4-triazoles 3.The yields are excellent and the position selectivity is high.The structures of the 1,2,4-triazole derivatives were determined with the aid of proton-coupled 13C-NMR. spectra.