27700-58-9

Usage

Molecular Structure

A heterocyclic organic compound with a carbonitrile and amino group attached to the imidazole ring, and a methyl group at the 1-position.

Potential Uses

May be used in pharmaceutical research and drug development due to its unique structure and potential biological activity.

Applications

May have applications in organic synthesis and as a building block for the creation of other complex organic molecules.

Further Research

More research and study are needed to fully understand the potential uses and properties of this chemical compound.

Upstream product

• 117879-27-3 5-amino-1-methylimidazole-4-thiocarboxamide 
• 129877-98-1 5-azido-1-methyl-1H-imidazole-4-carbonitrile 
• 5098-11-3 5-amino-1H-imidazole-4-carbonitrile 
• 74-88-4 methyl iodide 
• 163729-65-5 5-amino-2-chloro-1-methyl-1H-imidazole-4-carboxamide 
• 5098-14-6 2-aminomalononitrile p-toluenesulfonate 
• 122-51-0 orthoformic acid triethyl ester 
• 74-89-5 methylamine 
• 129878-00-8 1-methoxy-9-methyl-2-azaadenine hydroiodide 
• 163729-67-7 methyl 5-azido-1-methyl-1H-imidazole-4-carboximidate 
• 163729-68-8 methyl 5-azido-1-methyl-1H-imidazole-4-carboxylate 
• 33174-57-1 5-amino-N'-methoxy-1-methylimidazole-4-carboxamidine 

Downstream Products

• 2697-28-1 6-chloro-N,N,9-trimethyl-9H-purin-2-amine 
• 1610624-74-2 C₁₂H₁₀N₄O₂ 
• 1610624-75-3 C₁₂H₁₀N₄O₃ 
• 1610624-76-4 C₁₂H₁₀N₄O₃ 
• 1610624-77-5 C₁₂H₁₀N₄O₃ 

Relevant academic research and scientific papers

Synthesis and radical scavenging activity of phenol-imidazole conjugates

Novel hydroxylated benzylideneamino imidazole derivatives were synthesized and their radical scavenging activity was assessed against DPPH and hydroxyl radicals. In the DPPH assay, most of the synthesized compounds showed an IC 50 in the range

A short and facile synthesis for Heteromine A

The first and efficient synthesis of the new pyrinium natural product Heteromine A, involving 5-amino-4-cyano-1-methylimidazole and N,N-dimethyldichlomethyleniminium chloride is reported.

Purines. LXIV syntheses of 9-methyl-2-azaadenine 1-oxide, its O-methyl derivative, and 1-substituted 5-azidoimidazole-4-carboxamides

Diazotization of 5-amino-N'-methoxy-1-methylimidazole-4-carboxamidine (4a) with NaNO2, in 1 N aqueous HCl was found to give the 1-methoxy-2-azaadenine derivative 8a · HI, which produced 5-azido-1-methylimidazole-4-carbonitrile (5a) on treatment with aqueous Na2CO3. The ribosyl analogue 5b, obtained from the riboside 4b by similar diazotization, was utilized for the synthesis of 5-azido-1-β-D-ribofuranosylimidazole-4-carboxamide (9b), a novel AICA riboside analogue. On heating in HCONMe2 at 700C for 10 min, 8a · HI yielded the 1-N-oxide 7a. Several reactions to transform the functional groups in 5a were also investigated.

A UNIQUE TRANSFORMATION OF 5-AMINO-N'-METHOXYIMIDAZOLE-4-CARBOXAMIDINES BY DIAZOTIZATION: SYNTHESIS OF THE 5-AZIDO ANALOGUE OF AICA RIBOSIDE

Diazotization of 1-substituted 5-amino-N'-methoxyimidazole-4-carboxamidines (I) was found to give the 5-azidoimidazole-4-carbonitriles II through the 1-methoxy-2-azaadenine intermediates IV.The product IIb from the riboside Ib was utilized for the synthesis of 5-azido-1-β-D-ribofuranosylimidazole-4-carboxamide (Vb), a novel AICA riboside analogue.