96960-71-3

Upstream product

• 96960-72-4 5-Acetylamino-1H-imidazole-4-carboxamide hydrochloride 
• 62-53-3 aniline 

Downstream Products

• 115043-37-3 N⁶-phenyl-2-methyladenosine 
• 119812-71-4 4-O-Acetyl-2,3-dideoxy-3-tetrabromophthalimido-1-<9-(6-phenylamino-2-methylpurinyl)>-β-D-threo-pentopyranose 
• 104091-31-8 (2R,4R,5S)-4-(2-Methyl-6-phenylamino-purin-9-yl)-tetrahydro-pyran-2,5-diol 
• 104091-21-6 (2S,4R,5S)-4-(2-Methyl-6-phenylamino-purin-9-yl)-tetrahydro-pyran-2,5-diol 

Relevant academic research and scientific papers

Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK)

The present invention relates to a method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) and the use of the compounds in the prevention or treatment of disease, including pre-diabetes, type 2 diabetes, syndrome X, metabolic syndrome and obesity.

SUBSTITUTED 6-ANILINOPURINE DERIVATIVES AS INHIBITORS OF CYTOKININ OXIDASE/DEHYDROGENASE AND PREPARATIONS CONTAINING THESE DERIVATIVES

The invention relates to substituted 6-anilinopurine derivatives of the general formula I, wherein R denotes one to five substituents independently selected from the group consisting of hydrogen, halogen, hydroxyl, amino, alkyloxy and alkyl group, and R2 denotes amino, halogen, nitro, thio, alkylthio or alkyl group for use as inhibitors of cytokinin oxidase/dehydrogenase. The invention also relates to the compositions containing these derivatives.

Phosphorus Pentoxide in Organic Synthesis, XVI. - A One-step Synthesis of 2-Methyl-N6-aryladenines from 5-Acetylamino-1H-imidazole-4-carboxamide Hydrochloride

5-Amino-1H-imidazole-4-carboxamide hydrochloride has been converted into a series of 2-methyl-6-(arylamino)purines 3 via 5-acetylamino-1H-imidazole-4-carboxamide hydrochloride (1) which was heated with phosphorus pentoxide, triethylamine hydrochloride, and an appropriate substituted aniline at 180 deg C.