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Usage

Uses

Used in Pharmaceutical Synthesis:
1-(4-(4-aminobenzyl)piperazin-1-yl)ethanone is utilized as a key building block in the creation of various pharmaceuticals. Its diverse reactivity and functional group compatibility make it an essential component in the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
In the realm of organic chemistry, 1-(4-(4-aminobenzyl)piperazin-1-yl)ethanone serves as a vital intermediate for synthesizing a wide range of organic compounds. Its structural and chemical properties facilitate the formation of complex molecules and contribute to the advancement of organic synthesis techniques.
Used in Medicinal Chemistry and Drug Discovery:
Due to its potential biological activity, 1-(4-(4-aminobenzyl)piperazin-1-yl)ethanone is employed in medicinal chemistry and drug discovery. Researchers leverage its unique properties to design and develop novel therapeutic agents, potentially leading to the creation of innovative treatments for various diseases and conditions.
Used in Chemical and Biochemical Research:
The unique structure and properties of 1-(4-(4-aminobenzyl)piperazin-1-yl)ethanone make it a valuable tool for investigating chemical and biochemical processes. It can be used to study molecular interactions, reaction mechanisms, and the behavior of different functional groups, thereby enhancing our understanding of complex chemical systems.

Downstream Products

• 1142946-71-1 1-(4-(4-(4-(4-methylthiophen-2-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)benzyl)piperazin-1-yl)ethanone 

Relevant academic research and scientific papers

PYRROLOPYRIMIDINE COMPOUNDS AND THEIR USE AS JANUS KINASE MODULATORS

Provided herein are pyrrolopyrimidine compounds of Formula (I) wherein R1 is a heteroaryl containing at least one S atom, and optionally substituted on a ring carbon by one, two, or three substituents each independently selected from the group consisting of : halo, hydroxyl, nitro, formyl, formamido, cyano, sulfonyl, carboxy, amino, amido, acylamino, carbamoyl, sulphamoyl, alkyl, alkenyl, CF3, ureido, alkynyl, alkoxy, alkanoyl, alkoxycarbonyl, carbaldehyde oxime, N -alkylsulphamoyl, N-alkylcarbamoyl, -OR13R11 or -R13R11; R2 is phenyl or pyridinyl, wherein R2 optionally substituted on a ring carbon by one, two, or three substituents each indenpendently selected from the group consisting of : halo, hydroxyl, cyano, nitro, formyl, formamido, carboxy, sulfonyl, amino, amido, -N- alkyl -amino, carbamoyl, sulphamoyl, CF3, ureido, alkyl, alkenyl, alkynyl, alkoxy, alkanoyl, alkoxycarbonyl, N-alkylsulphamoyl, N-alkylcarbamoyl, -OR11, -OR12R11, or -R12R11; and methods of making and using the same. Such compounds may be used in inflammatory or myeloproliferative disorders. The disclosure also provides for treating cancer.