76006-01-4

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(5-Methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)is used as a potential pharmaceutical candidate for [application reason] due to its structural features and potential interactions with biological targets. Its pharmacological properties may contribute to the development of new drugs or therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Ethanone, 1-(5-Methyl-1H-pyrazolo[3,4-c]pyridin-1-yl)is utilized as a compound of interest for [application reason]. Its unique structure and potential interactions with biological targets make it a valuable subject for further research and exploration of its properties and effects.

Upstream product

• 76005-97-5 5-acetamido-2,4-dimethylpyridine 
• 1193-71-1 5-amino-2,4-dimethylpyridine 

Downstream Products

• 76006-06-9 5-methyl-1H-pyrazolo[3,4-c]pyridine 

Relevant academic research and scientific papers

Thrombin inhibitors

Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions having the following structure: or a pharmaceutically acceptable salt thereof, wherein b is NY or O; c is CY2or N; d is CY3or N; e is CY4or N; f is CY5or N; g is CY6or N; Y4, Y5, and Y6are independently hydrogen, C1-4alkyl, or halogen; Y1and Y2are independently hydrogen, C1-4alkyl, C3-7cycloalkyl, halogen, NH2, OH or C1-4alkoxy, and Y3is hydrogen, C1-4alkyl, C3-7cycloalkyl, halogen, —CN, NH2, OH or C1-4alkoxy; A is and W, W1, R1, R3, R4, R5, X and Z are defined in the specification.

Pyrazolopyridines. Part 5. Preparation and Reactions of Pyrazolopyridines

A series of pyrazolopyridines has been prepared by nitrosation of 3-acetamido-4-methylpyridines and subsequent rearrangement and cyclisation of the N-acetyl-N-nitroso-compounds produced.The reactions of the pyrazolopyridines have been investigated. 1- and 2-Acetyl and 1- and 2-benzyl compounds were obtained and their structures elucidated spectroscopically.The ring system readily undergoes electrophilic substitution in the 3-position. 7-Chloropyrazolopyridine has been shown to be more susceptible to nucleophilic substitution than the isomeric 5-chloro-compound.