Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities
Тип публикации: Journal Article
Дата публикации: 2022-07-20
SCImago Q3
WOS Q3
БС2
SJR: 0.334
CiteScore: 3.3
Impact factor: 1.8
ISSN: 09743626, 09737103, 02534134
General Chemistry
Краткое описание
It was observed that when two prominent bioactive compounds fused together, the new hybrid showed much more promising possessions. Aiming this, here we have fused pyrazolo[1,5-a]pyrimidines with ferrocene, both of which are popularly known as the bio-active molecular core, employing a very simple and facile synthetic strategy using a mild acid KHSO4 as a catalyst under ultrasonic irradiation. The structures of these synthesized novel compounds were confirmed by their spectral and analytical data. The single-crystal X-ray crystallographic analysis of a selected compound reveals that the 7-ferrocenyl-pyrazolo[1,5-a]pyrimidine (C22H16ClFeN3) hybrid interestingly exists as a dimer and forms a triclinic crystal system with P1 space group (no. 2), a = 7.554(3) Å, b = 13.650(6) Å, c = 18.444(8) Å, α = 96.938(7)o, β = 90.034(7)o, γ = 106.015(6)o, V = 1813.5(14) Å3, Z = 4, µ(MoKα)= 0.990 mm−1, wavelength = 0.71073 Å, Dcalc = 1.515 g/cm3 with 42808 measured reflection (4.452° ≤ 2θ ≤ 58.312°), 9524 unique reflections (Rint = 0.1267, Rsigma = 0.1390) were used in all the calculations. The final R1 obtained was 0.0570 (I>2σ(I)) with wR2 = 0.1656 for all data. Most of the compounds exhibited encouraging antioxidant activities like compounds 3b-c, 3k-l and 3n exhibited prominent nitric-oxide scavenging activities, while compounds 3a-d, 3g, 3k, 3n, and 3o are promising DPPH-scavengers. Compounds 3i-k and 3m exhibited antibacterial activities at MIC of 500 µg/mL, while 3p exhibited activities at MIC of 250 µg/mL. Five of the compounds, 3i-k, 3m, and 3p, were found to possess anti-biofilm activities against both Gram-positive and Gram-negative bacteria. Synopsis: Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids were synthesized and investigated for their anti-oxidant, anti-bacterial and anti-biofilm properties. Almost all of the new compounds mentioned have anti-oxidant capabilities and a few of them also exhibited anti-bacterial and anti-biofilm properties
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Das S. et al. Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities // Journal of Chemical Sciences. 2022. Vol. 134. No. 3. 79
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Das S., Borkotoky S., Rymbai M., Borah V. V., Roy J. D., Kaping S., HELISSEY P., Vishwakarma J. N. Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities // Journal of Chemical Sciences. 2022. Vol. 134. No. 3. 79
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TY - JOUR
DO - 10.1007/s12039-022-02064-y
UR - https://doi.org/10.1007/s12039-022-02064-y
TI - Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities
T2 - Journal of Chemical Sciences
AU - Das, Susma
AU - Borkotoky, Shivangi
AU - Rymbai, Maxmillando
AU - Borah, Vedant V
AU - Roy, Jayanti D
AU - Kaping, Shunan
AU - HELISSEY, PHILIPPE
AU - Vishwakarma, Jai N
PY - 2022
DA - 2022/07/20
PB - Springer Nature
IS - 3
VL - 134
SN - 0974-3626
SN - 0973-7103
SN - 0253-4134
ER -
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@article{2022_Das,
author = {Susma Das and Shivangi Borkotoky and Maxmillando Rymbai and Vedant V Borah and Jayanti D Roy and Shunan Kaping and PHILIPPE HELISSEY and Jai N Vishwakarma},
title = {Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities},
journal = {Journal of Chemical Sciences},
year = {2022},
volume = {134},
publisher = {Springer Nature},
month = {jul},
url = {https://doi.org/10.1007/s12039-022-02064-y},
number = {3},
pages = {79},
doi = {10.1007/s12039-022-02064-y}
}
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