93758-44-2

Usage

Uses

Used in Pharmaceutical Industry:
3-Piperidinecarboxylic acid, 1-methyl-2,4-dioxo-, ethyl ester is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structure of drugs, enhancing their therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Piperidinecarboxylic acid, 1-methyl-2,4-dioxo-, ethyl ester serves as an intermediate in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Organic Synthesis:
3-Piperidinecarboxylic acid, 1-methyl-2,4-dioxo-, ethyl ester is used as a reagent in organic synthesis for the preparation of various organic compounds, facilitating the creation of new molecules with potential applications.
Used in Research and Development:
As a building block in the production of new molecules with biological activity, 3-Piperidinecarboxylic acid, 1-methyl-2,4-dioxo-, ethyl ester is utilized in research and development to explore and innovate novel chemical entities with potential therapeutic or practical uses.

Upstream product

• 851726-48-2 ethyl 3-((3-ethoxy-3-oxopropyl)(methyl)amino)-3-oxopropanoate 
• 1426943-75-0 C₁₀H₁₇NO₅ 

Downstream Products

• 19686-05-6 2.8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole 
• 1426943-76-1 1-methyl-4-(p-tolylamino)-5,6-dihydropyridin-2(1H)-one 
• 93758-08-8 1,2,3,4,6,7,8,9-octahydro-1,6-dioxo-2-methyl-5-(2-methoxy-5-cyanophenoxy)-9-carbethoxyisoquinoline 

Relevant academic research and scientific papers

Constructions of tetrahydro-γ-carboline skeletons via intramolecular oxidative carbon-carbon bond formation of enamines

The synthetically and biologically important 4-methyl and 4-methoxy tetrahydro-γ-carboline compounds were readily synthesized in high yields from an aryl amine and a 5-amino-3-oxopentanoate derivative through a series of reactions of enamination, oxidative annulation, deprotection/lactamization and the final reduction reaction of the carbonyl group. The underpinning strategy involves the oxidative C(sp2)-C(sp2) bond formation realized by either Pd(OAc)2/Cu(OAc)2 or a hypervalent iodine reagent.