新型N-酰基-7-甲氧基-苯并[4,5]噻唑并[2,3-c][1,2,4]三唑-3(2H)-硫酮的合成及其除草活性
收稿日期: 2013-08-01
修回日期: 2013-10-03
网络出版日期: 2013-10-11
基金资助
国家自然科学基金(No.30900959)资助项目.
Synthesis and Herbicidal Activity of Novel N-Acyl-7-methoxybenzo[4,5]thiazolo- [2,3-c][1,2,4]triazole-3(2H)-thione
Received date: 2013-08-01
Revised date: 2013-10-03
Online published: 2013-10-11
Supported by
Project supported by the National Natural Science Foundation of China (No. 30900959).
为了寻找新的含苯并噻唑稠杂环农药先导化合物,以2-氨基-6-甲氧基苯并噻唑为起始原料,经肼化、环化和酰基化反应,合成出了14个N-酰基-7-甲氧基苯并[4,5]噻唑并[2,3-c][1,2,4]三唑-3(2H)-硫酮,并利用1H NMR,ESI-MS及元素分析对其结构进行表征. 对目标化合物进行初步的除草活性筛选,实验结果表明:在浓度为200 mg/L时,大部分化合物对黄瓜(Cucumis sativus)、小麦(Triticum aestivum)、高粱(Sorghum vulgare)、萝卜(Raphanus sativus)、油菜(Brassica campestris)和稗草(Echinochloa crusgalli)的根和茎的抑制率在85%以上.
王海林 , 阮铃莉 , 陈勇 , 刘幸海 , 翁建全 . 新型N-酰基-7-甲氧基-苯并[4,5]噻唑并[2,3-c][1,2,4]三唑-3(2H)-硫酮的合成及其除草活性[J]. 有机化学, 2014 , 34(2) : 419 -423 . DOI: 10.6023/cjoc201308001
In order to find the new fused heterocycle of benzothiazole lead compounds, fourteen novel N-acyl-7-methoxybenzo[4,5]thiazolo[2,3-c][1,2,4]triazole-3(2H)-thiones were synthesized by using 6-methoxybenzo[d]thiazol-2-amine as starting materials via hydrazine, cyclization and acylation. The structures of the target compounds were characterized by 1H NMR, ESI-MS and elemental analysis. The synthesized target compounds were screened for the herbicidal activity. The results indicated that the inhibition effects of most target compounds on the root and stem of Cucumis sativus, Triticum aestivum, Sorghum vulgare, Raphanus sativus, Brassica campestris and Echinochloa crusgalli were more than 85% at 200 mg/L.
[1] Liu, X.-H.; Zhao, W.-G.; Wang, B.-L.; Li, Z.-M. Chem. Res. Intermed. 2012, 38, 1999.
[2] Luo, Y.; Chen, T.-F.; Huang, X.-C.; Wang, Y.; Huang, M.-C.; Zheng, W.-J. Acta Chim. Sinica 2012, 70, 1295 (in Chinese).
(罗懿, 陈填烽, 黄晓纯, 王弋, 黄荫成, 郑文杰, 化学学报, 2012, 70, 1295.)
[3] Liu, X.-H.; Weng, J.-Q.; Tan, C.-X. J. Chem. 2013, 2013, 306361.
[4] Lu, Y.-M.; Qu, Z.-B.; Hu, W.; Yue, X.-Y. Acta Chim. Sinica 2012, 70, 973 (in Chinese).
(卢艳梅, 区志镔, 胡伟, 乐学义, 化学学报, 2012, 70, 973.)
[5] Weng, J.-Q.; Tan, C.-X.; Liu, X.-H. J. Pestic. Sci. 2012, 37, 164.
[6] Weng, J.-Q.; Huang, H.; Tan, C.-X.; Liu, X.-H.; Chu, W.-S.; Chen, J. Chin. J. Org. Chem. 2012, 32, 957 (in Chinese).
(翁建全, 黄华, 谭成侠, 刘幸海, 储为盛, 陈杰, 有机化学, 2012, 32, 957.)
[7] Weng, J.-Q.; Huang, H.; Yu, Z.-Q.; Zhang, H.-M.; Tan, C.-X.; Liu, X.-H. Asian J. Chem. 2012, 24, 561.
[8] Chen, C.-X.; Li, X.-Q.; Li,T.-C.; Zhou, X.-Z. Acta Chim. Sinica 2012, 70, 852 (in Chinese).
(陈凑喜, 李学强, 李天才, 周学章, 化学学报, 2012, 70, 852.)
[9] Weng, J.-Q.; Liu, X.-H.; Zhang, G.-F.; Tan, C.-X.; Ding, C.-R.; Ou, X.-M. Chin. J. Org. Chem. 2011, 31, 374 (in Chinese).
(翁建全, 刘幸海, 张国富, 谭成侠, 丁成荣, 欧晓明, 有机化学, 2011, 31, 374.)
[10] Weng, J.-Q.; Liu, X.-H.; Huang, H.; Tan, C.-X.; Chen, J. Molecules 2012, 17, 989.
[11] Michael, G.; Gabriele, D.; Wilfried, F.; Gerhard, J.; Richard, R. US 5424443, 1995 [Chem. Abstr. 1993, 118, 101946].
[12] Li, Y.-J.; Li, C.-Y.; Ji, N.; Sun, S.-Q.; Zhou, X.-X. Acta Chim. Sinica 2012, 70, 151 (in Chinese).
(李英俊, 李春燕, 靳焜, 孙淑琴, 周晓霞, 化学学报, 2012, 70, 151.)
[13] David, P. C.; Roy, V. E.; Roy, T. H. J. Agric. Food Chem. 1981, 29, 640.
[14] Schmidt, T. DE 3038636, 1982 [Chem. Abstr. 1982, 97, 127633].
[15] Guan, W.-B.; Zhang, H.-Y. Int. J. Environ. Anal. Chem. 2013, 93, 679.
[16] Handte, R.; Hoerlein, G.; Koecher, H. US 4130413, 1978. [Chem. Abstr. 1978, 88, 190816].
[17] Siddiqui, S. M.; Salahuddin, A.; Azam, A. Bioorg. Med. Chem. Lett. 2012, 22, 2768.
[18] Feng, C.-J. Acta Chim. Sinica 2012, 70, 512 (in Chinese).
(冯长君, 化学学报, 2012, 70, 512.)
[19] Weng,J.-Q.; Wang, L; Liu, X.-H. J. Chem. Soc. Pakistan 2012, 34, 1248.
[20] Yan, C.-M.; Zhu, C.-W. Modern Agrochem. 2006, 5, 11 (in Chinese).
(严传鸣, 朱长武, 现代农药, 2006, 5, 11.)
[21] Ziegler, H.; Benen-Buchhoolz, J.; Etzel, W. Pflanzenschutz-Nachr. Bayer 2003, 56, 213.
[22] Song, L.-L.; Geng, L.-W.; Yang, B.-L.; Ding, Y.-W.; Ma, J.-B. Modern Agrochem. 2012, 11, 11 (in Chinese).
(宋丽丽, 耿丽文, 杨丙连, 丁亚伟, 马金波, 现代农药, 2012, 11, 11.)
[23] Barnett, C. J. US 3937714, 1976 [Chem. Abstr. 1976, 84, 135634].
[24] Swamy, D. K.; Deshmukh, M. V. J. Chem. Pharm. Res. 2010, 2, 167.
[25] Xue, Y.-L.; Liu, X.-H.; Zhang, Y.-G. Asian J. Chem. 2012, 24, 1571.
[26] Xue, Y.-L.; Zhang, Y.-G.; Liu, X.-H. Asian J. Chem. 2012, 24, 3016.
[27] Xue, Y.-L.; Zhang, Y.-G.; Liu, X.-H. Asian J. Chem. 2012, 24, 5087.
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