Synthesis of isatin, 5-chloroisatin and their Δ<sup>2</sup>-1,3,4 oxadiazoline derivatives for comparative cytotoxicity study on brine shrimp
DOI:
https://doi.org/10.3329/bjp.v2i1.494Keywords:
Chloroisatin, Cytotoxicity, OxadiazolineAbstract
Isatin (3a), isatin 3-carbohydrazone (4a), 5-spiro (isatin) 2-(N-acetyl hydra-zino) 4-(N-acetyl)-?2-1,3,4 oxadiazoline (5a), and 5-spiro (isatin) 2-hydrazino-?2-1,3,4 oxadiazoline (6a) had been synthesized from the unsubstituted oximinoacetanilide (2a). 4-Chlorooximinoacetanilide (2b), 5-chloroisatin (3b), 5-chloroisatin 3-carbohydrazone (4b) and 5-spiro (5¢-chloroisatin) 2-(N-acetyl hydrazino) 4-N-acetyl ?2-1,3,4 oxadiazoline (5b) compounds had been synthesized from p-chloroaniline. The structures of the products had been characterized from the spectral analysis and comparative cytotoxicity study of them was studied.
Downloads
313
197 Read
17
References
Islam MR, Khayer K, Shaha G, Chowdhury MSK. Syntheses of thiocarbohydrazide, some thiocarbo-hydrazones and their cyclized products as probes for pharmacological studies. Indian. J Chem. 1992; 31B: 547.
Islam MR, Khayer K, Abedin MJ. Reaction of isatin with 2-aminophenol leading to spiroheterocycles having anticancer activity. Jahangirnagar Univ J Sci. 2001; 24: 17.
Lingcon MH, Islam R, Khayer K, Islam MR. Cyclization of substituted indole-2-one-3-thiosemicarbazones to noble heterocyclic systems. J Bangladesh Chem Soc. 2001; 14: 127.
Islam R. Indian. J Chem. 2001; 40B: 240.
Kubota S, Yasufumi U, Fujikane K, Toyooka K, Shibuya M. Synthesis of 4-acyl-2-(acylamino)-D2-1,3,4-thiadiazolines and 4-acyl-2-amino-D2-1,3,4-thiadiazolines by acylation of thiosemicarbazones. J Org Chem. 1980; 45: 1473.
Islam MR, Khayer K, Islam R. Jahangirnagar Univ J Sci. 1997; 21: 1.
Microwell A. Cytotoxicity assay using Artemia salina (brine shrimp). Planta Med. 1997; 59: 250.
Additional Files
How to Cite
Issue
Section
License
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).