20870-91-1

Usage

Uses

Used in Organic Synthesis:
5-Amino-1-methyl-2-oxoindoline is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a versatile building block for the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Amino-1-methyl-2-oxoindoline is used as a starting material for the synthesis of various drug candidates. Its bioisosteric similarity to indole and indazole systems allows for the development of novel compounds with potential therapeutic applications.
Used in Agrochemical Industry:
5-Amino-1-methyl-2-oxoindoline is also utilized in the agrochemical industry for the synthesis of active ingredients in pesticides and other crop protection products. Its unique chemical properties enable the creation of new molecules with improved efficacy and selectivity.
Used in Specialty Chemicals:
5-Amino-1-methyl-2-oxoindoline serves as a valuable intermediate in the production of specialty chemicals, such as dyes, pigments, and other performance-enhancing additives. Its reactivity and functional group compatibility make it suitable for various chemical transformations and applications.

InChI:InChI=1/C9H10N2O/c1-11-8-3-2-7(10)4-6(8)5-9(11)12/h2-4H,5,10H2,1H3

Upstream product

• 20870-89-7 1-methyl-5-nitro-1,3-dihydro-indol-2-one 
• 100-15-2 N-methyl(p-nitroaniline) 
• 2653-16-9 2-chloro-N-methyl-N-(4-nitrophenyl)acetamide 
• 61-70-1 N-methyl-2-indolinone 

Relevant academic research and scientific papers

SUBSTITUTED ARYLSULFONYLAMINOMETHYLPHOSPHONIC ACID DERIVATIVES, THEIR PREPARATION AND THEIR USE IN THE TREATMENT OF TYPE I AND II DIABETES MELLITUS

The present invention relates to substituted arylsulphonylaminomethylphosphonic acid derivatives of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof which ha

INHIBITORS OF FOCAL ADHESION KINASE

The invention provides inhibitors of focal adhesion kinase, an enzyme involved in the attachment of the cytoskeleton of a cell to an extracellular matrix, which has been implicated in processes such as cell migration, cell proliferation, and cell survival. The inhibitors are derivatives of a 5-substituted 2,4-diaminopyridine wherein the substituents are as defined herein. The invention also provides a method of using the inhibitors in treatment of cancer, and methods of preparation of the inhibitors by use of coupling reactions.

Oxazolidinones containing oxindoles as antibacterial agents

The present invention relates to novel oxazolidinones derivatives of oxindoles of formula I, or a pharmaceutically acceptable salt thereof wherein Y1 is —CH— or —CF—; R1 is —C1-4alkyl, optionally substituted with a fluoro atom, or R1 is —C3-5cycloalkyl; and R2 is —H or —CH3. These compounds are useful as antibacterial agents.

Oxindole oxazolidinone as antibacterial agent

The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof wherein R1 is C1-4alkyl, optionally substituted with a fluoro atom, or R1 is a cyclopropyl or cyclopropylmethyl; and R2 is methyl or ethyl. The compound is useful as antibacterial agents.