Synthesis and Antibacterial Study of 4-(2-Aminoethyl) morpholine Derivatives
Received 10 Mar, 2016 |
Accepted 22 Jun, 2016 |
Published 28 Sep, 2016 |
Because of broad spectrum of biological activities bysulfamoyl group, a series of 4-(2-(N-(2-chlorobenzyl/4- bromobenzyl) arylsulfamoyl) ethyl)morpholine, 6a-d/7a-d, have been synthesized from4-(2-aminoethyl)morpholine (1). First step includes the synthesis of4-(2-(arylsulfamoyl) ethyl)morpholine, 3a-d,by reaction of(1) andarylsulfonyl chlorides, 2a-d, in water under definite pH control by 10% Na2CO3. In the second step, the molecules 3a-d were converted to 6a-d and 7a-don reaction with 2-chlorobenzyl chloride (4) and 4-bromobenzyl bromide(5), respectively, in DMF in the presence of NaH. Using IR,1H-NMR and EI-MS spectral records, the proposed molecular structures were verified.The antibacterial activity results showed good inhibitory action against all the bacterial strains of gram-bacteria with a few exceptions like B. subtilis.
How to Cite this paper?
APA-7 Style
Rehman,
A.U., Masih,
Y., Abbasi,
M.A., Siddiqui,
S.Z., Hussain,
T., Rasool,
S. (2016). Synthesis and Antibacterial Study of 4-(2-Aminoethyl) morpholine Derivatives. Pakistan Journal of Chemistry, 6(1-2), 10-15. https://doi.org/10.15228/2016.v06.i01-2.p02
ACS Style
Rehman,
A.U.; Masih,
Y.; Abbasi,
M.A.; Siddiqui,
S.Z.; Hussain,
T.; Rasool,
S. Synthesis and Antibacterial Study of 4-(2-Aminoethyl) morpholine Derivatives. Pak. J. Chem. 2016, 6, 10-15. https://doi.org/10.15228/2016.v06.i01-2.p02
AMA Style
Rehman
AU, Masih
Y, Abbasi
MA, Siddiqui
SZ, Hussain
T, Rasool
S. Synthesis and Antibacterial Study of 4-(2-Aminoethyl) morpholine Derivatives. Pakistan Journal of Chemistry. 2016; 6(1-2): 10-15. https://doi.org/10.15228/2016.v06.i01-2.p02
Chicago/Turabian Style
Rehman, Aziz, Ur, Y. Masih, M. A. Abbasi, S. Z. Siddiqui, T. Hussain, and S. Rasool.
2016. "Synthesis and Antibacterial Study of 4-(2-Aminoethyl) morpholine Derivatives" Pakistan Journal of Chemistry 6, no. 1-2: 10-15. https://doi.org/10.15228/2016.v06.i01-2.p02
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