Email this article Synthesis of Macrocyclic Ttipeptidopyridine Schiff Base Candidates
- Authors: Sallam H.A.1, Abdel-Mageid R.E.2, Amr A.E.3,4
-
Affiliations:
- Synthetic Organic Lab, Chemistry Department, Faculty of Science
- Department of Photochemistry
- Pharmaceutical Chemistry Department, College of Pharmacy, Drug Exploration and Development Chair (DEDC)
- Applied Organic Chemistry Department
- Issue: Vol 89, No 11 (2019)
- Pages: 2308-2313
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223177
- DOI: https://doi.org/10.1134/S1070363219110239
- ID: 223177
Cite item
Open Access
Access granted
Subscription Access
Abstract
In the current study, a series of macrocyclic tripeptide Schiff bases 2–6 were synthesized by using macrocyclic tripeptide hydrazide 1 as starting material. Treatment of hydrazide 1 with active carbonyl cycloalkanones gave cycloalkanone hydrazines 2a–2d. Also, condensation of 1 with aromatic and heterocyclic aldehydes, or aromatic and heterocyclic acetyl derivatives afforded the corresponding Schiff base candidates 3a–3e, 4a–4c, 5a–5c, and 6a–6c, respectively.
About the authors
H. A. Sallam
Synthetic Organic Lab, Chemistry Department, Faculty of Science
Email: aamr@ksu.edu.sa
Egypt, Abbassia, Cairo, 11566
R. E. Abdel-Mageid
Department of Photochemistry
Email: aamr@ksu.edu.sa
Egypt, Dokki, Cairo, 12622
A. E. Amr
Pharmaceutical Chemistry Department, College of Pharmacy, Drug Exploration and Development Chair (DEDC); Applied Organic Chemistry Department
Author for correspondence.
Email: aamr@ksu.edu.sa
Saudi Arabia, Riyadh, 11451; Dokki, Cairo, 12622
