Rubab, Kaniz and Abbasi, Muhammad A. and Rehman, Aziz-ur and Siddiqui, Sabahat Zahra and Akhtar, Muhammad Nadeem (2016) S-Alkylated/aralkylated 2-(1H-indol-3-yl-methyl)-1,3,4- oxadiazole-5-thiol derivatives. 1. Synthesis and Characterization. Tropical Journal of Pharmaceutical Research, 15 (7). pp. 1515-1524. ISSN 1596-5996 (print); 1596-9827 (online). (Published)
|
PDF
fist-2016-nadeem-S-Alkylatedaralkylated 2-(1H-indol-3-yl-methyl)-1,3,44.pdf Download (612kB) | Preview |
Abstract
Purpose: To synthesize and characterize S-alkylated/aralkylated 2-(1H-indol-3-ylmethyl)-1,3,4- oxadiazole-5-thiol derivatives. Methods: 2-(1H-indol-3-yl)acetic acid (1) was reacted with absolute ethanol and catalytic amount of sulfuric acid to form ethyl 2-(1H-indol-3-yl)acetate (2) which was transformed to 2-(1H-indol-3- yl)acetohydrazide (3) by refluxing with hydrazine hydrate in methanol. Ring closure reaction of 3 with carbon disulfide and ethanolic potassium hydroxide yielded 2-(1H-indol-3-ylmethyl)-1,3,4-oxadiazole-5- thiol (4) which was finally treated with alkyl/aralkyl halides (5a-u) in DMF and NaH to yield Salkylated/ aralkylated 2-(1H-indol-3-ylmethyl)-1,3,4-oxadiazole-5-thiols (6a-u). Structural elucidation was done by IR, 1H-NMR and EI-MS techniques Results: 2-(1H-indol-3-ylmethyl)-1,3,4-oxadiazole-5-thiol (4) was synthesized as the parent molecule and was characterized by IR and the spectrum showed peaks resonating at (cm-1) 2925 (Ar-H), 2250 (S-H ), 1593 (C=N ) and 1527 (Ar C=C ); 1H-NMR spectrum showed signals at δ 11.00 (s, 1H, NH-1ʹ), 7.49 ( br.d, J = 7.6 Hz, 1H, H-4'), 7.37 (br.d, J = 8.0 Hz, 1H, H-7'), 7.34 (br.s, 1H, H-2'), 7.09 (t, J = 7.6Hz, 1H, H-5'), 7.00 (t, J = 7.6 Hz, 1H, H-6') and 4.20 (s, 2H, CH2-10ʹ). EI-MS presented different fragments peaks at m/z 233 (C11H9N3OS)˙+ [M+2]+, 231 (C11H9N3OS)˙+ [M]+, 158 (C10H8NO)+, 156 (C10H8N2)˙+, 130 (C9H8N)+. The derivatives (6a-6u) were prepared and characterized accordingly. Conclusion: S-alkylated/aralkylated 2-(1H-indol-3-ylmethyl)-1,3,4-oxadiazole-5-thiols (6a-u) were successfully synthesized.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | 2-(1H-indole-3-ylmethyl)-1,3,4-oxadiazole-5-thiol, S-alkylated/aralkylated derivatives, Synthesis, Characterization, 1H-NMR and EI-MS |
| Subjects: | Q Science > QR Microbiology |
| Faculty/Division: | Faculty of Industrial Sciences And Technology |
| Depositing User: | Noorul Farina Arifin |
| Date Deposited: | 23 Feb 2017 07:25 |
| Last Modified: | 19 Apr 2018 02:35 |
| URI: | http://umpir.ump.edu.my/id/eprint/16812 |
| Download Statistic: | View Download Statistics |
Actions (login required)
 |
View Item |