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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front Chem Eng Chin    2009, Vol. 3 Issue (2) : 186-191    https://doi.org/10.1007/s11705-009-0004-0
RESEARCH ARTICLE
Microwave-assisted synthesis and antimicrobial activities of 2-aryl-3-(naphthalene-1 or 2-yl)-1,3-thiazolidin-4-ones
Hua CHEN1(), Yanan LI1, Jie BAI1, Lian ZHAO1, Xiangguo YUAN1, Xiaoliu LI1,2(), Keqiang CAO3
1. Key Laboratory of Chemical Biology of Hebei Province, College of Chemistry and Environmental Science, Hebei University, Baoding, 071002, China; 2. Key Laboratory of Medicinal Chemistry and Molecular Diagnosis, Ministry of Education, Hebei University, Baoding,071002, China; 3. College of Plant Protection,Agricultural University, Baoding, Hebei 071001, China
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Abstract

2-aryl-3-(naphthalene-1 or 2-yl)-1,3-thiazolidin-4-ones 4 and 5 were synthesized in 41%-67% yield by using microwave-assisted one-pot protocol. The structures of the new compounds 4l, 4m, 5c, 5e, 5g, 5h, and 5j-5m were confirmed by IR, NMR, MS, and elemental analysis. The antimicrobial activities of the compounds against Pseudomonas syringae pv. lachrymans (Smith et Bryan) Young, Dye & Wilkie, Botrytis cinerea Pers., and Sphaerotheca fusca Blum. were examined. Some of the compounds showed good antifungical activity against Sphaerotheca fusca Blum.

Keywords microwave-assisted synthesis      naphthyl      thiazolidin-4-one      antimicrobial     
Corresponding Author(s): CHEN Hua,Email:hua-todd@hbu.cn; LI Xiaoliu,Email:lixl@hbu.cn   
Issue Date: 05 June 2009
 Cite this article:   
Xiangguo YUAN,Xiaoliu LI,Keqiang CAO, et al. Microwave-assisted synthesis and antimicrobial activities of 2-aryl-3-(naphthalene-1 or 2-yl)-1,3-thiazolidin-4-ones[J]. Front Chem Eng Chin, 2009, 3(2): 186-191.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-009-0004-0
https://academic.hep.com.cn/fcse/EN/Y2009/V3/I2/186
Fig.1  Condition 1 for : M.W., toluene, 140°C in 10 mL sealed vessel, 5 min
Condition 2 for : M.W., toluene, reflux, 20 min
Scheme 1 Microwave assisted synthesis of 2-aryl-3-(naphthalene-1 or 2-yl)-1,3-thiazolidin-4-ones
compoundsinhibition/%compoundsinhibition/%
C=1000 mg/LC=500 mg/LC=1000 mg/LC=500 mg/L
4g [18]60.753.75f1.8
4l 64.870.25g [18]60.750.9
4m 67.076.85h49.5
5a a)5i41.420.0
5b [18]20.639.65j
5c 17.15k38.63.0
5d 40.05l75.679.2
5e 5m91.693.0
10% difenoconazole WP (20 mg/L)63.8%
Tab.1  Inhibition of compounds on Blum
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