Continuously updated synthesis method about 50501-07-0

Here is just a brief introduction to this compound(50501-07-0)Related Products of 50501-07-0, more information about the compound(Ethyl indoline-2-carboxylate) is in the article, you can click the link below.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 50501-07-0, is researched, SMILESS is O=C(C1NC2=C(C=CC=C2)C1)OCC, Molecular C11H13NO2Journal, Journal of Chemical and Pharmaceutical Research called Synthesis and biological activity of alkyl-2-[5-(hydroxy-methyl)-5-nitro-2-oxo-1,3,2λ5-dioxaphosphinan-2-yl] amino acid esters, Author is Dadapeer, E.; Naidu, K. Reddi Mohan; Ramesh, M.; Raju, C. Naga; Devamma, M. Nagalakshmi, the main research direction is alkyl hydroxymethylnitrooxodioxaphosphinanyl amino acid ester preparation antibacterial antifungal activity.Related Products of 50501-07-0.

Synthesis of a series of new alkyl-2-[5-(hydroxymethyl)-5-nitro-2-oxo-1,3,2λ5-dioxaphosphinan-2-yl] amino acid esters was accomplished through a two-step process. The key step in the synthesis involves preparation of a dichloride intermediate, with different amino acid esters and with a few substituted phenols by reacting POCl3 in presence of Et3N in THF at 0-15°C. In the second step the intermediate in situ is treated with tris(hydroxymethyl)nitromethane (2-hydroxymethyl-2-nitro-1,3-propanediol) in the presence of Et3N at 40-45°C to form final products. The structures of final products were established by elemental anal., IR, 1H, 13C and 31P NMR and mass spectral data. The antimicrobial activity of these compounds was evaluated and they exhibited moderate antifungal and antibacterial activities.

Here is just a brief introduction to this compound(50501-07-0)Related Products of 50501-07-0, more information about the compound(Ethyl indoline-2-carboxylate) is in the article, you can click the link below.

Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics