Methyl 9-(2-Iminothiazol-3(2H)-yl)-9-oxononanoate-Reference-Cited by-同舟云学术

Methyl 9-(2-Iminothiazol-3(2H)-yl)-9-oxononanoate

Published:2023-02-04 Issue:1 Volume:2023 Page:M1580
ISSN:1422-8599
Container-title:Molbank
language:en
Short-container-title:Molbank

Author:

Micheletti Gabriele¹^ORCID,Calonghi Natalia²,Boga Carla¹^ORCID

Affiliation:

1. Department of Industrial Chemistry “Toso Montanari”, Alma Mater Studiorum-Università di Bologna, Viale Risorgimento 4, 40136 Bologna, Italy

2. Department of Pharmacy and Biotechnology, University of Bologna, Via Irnerio 48, 40126 Bologna, Italy

Abstract

Methyl 9-(2-iminothiazol-3(2H)-yl)-9-oxononanoate was synthesized through Schotten–Baumann type reaction between 2–aminothiazole and methyl 9-chloro-9-oxononanoate. The structure of the newly synthesized compound was elucidated based on 1H-NMR, 13C-NMR, DEPT, NOE, ESI-MS, FT-IR and UV-Vis spectroscopy.

Funder

Alma Mater Studiorum

Publisher

MDPI AG

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://www.mdpi.com/1422-8599/2023/1/M1580/pdf

Reference18 articles.

1. Monoazo disperse dyes—Part 1: Synthesis, spectroscopic studies and technical evaluation of monoazo disperse dyes derived from 2-aminothiazoles;Singh;Dyes Pigm.,2002

2. Synthesis, characterization and molecular docking studies of highly functionalized and biologically active derivatives of 2-aminothiazole;Kanagasabapathy;J. Mol. Struct.,2023

3. Synthesis and antimicrobial activity of novel structural hybrids of benzofuroxan and benzothiazole derivatives;Chugunova;Eur. J. Med. Chem.,2015

4. 2-Aminothiazole: A privileged scaffold for the discovery of anti-cancer agents;Wan;Eur. J. Med. Chem.,2021

5. Molecular salts of terephthalic acids with 2-aminopyridine and 2-aminothiazole derivatives as potential antioxidant agents; Base-Acid-Base type architectures;Khan;J. Mol. Struct.,2020