Chinese Journal of Organic Chemistry ›› 2024, Vol. 44 ›› Issue (11): 3446-3455.DOI: 10.6023/cjoc202403019 Previous Articles Next Articles
ARTICLE
赵薇a, 李凤宇a, 赵伟a, 查润a, 史彩华b, 徐志红a,*()
收稿日期:
2024-03-14
修回日期:
2024-05-11
发布日期:
2024-06-07
基金资助:
Wei Zhaoa, Fengyu Lia, Wei Zhaoa, Run Zhaa, Caihua Shib, Zhihong Xua,*()
Received:
2024-03-14
Revised:
2024-05-11
Published:
2024-06-07
Contact:
*E-mail:Supported by:
Share
Wei Zhao, Fengyu Li, Wei Zhao, Run Zha, Caihua Shi, Zhihong Xu. Design, Synthesis and Fungicidal and Nematocidal Activity of 1,2,3-Benzotriazine-4-one Oxadiazole Thioether (Sulfone) Methyl Derivatives[J]. Chinese Journal of Organic Chemistry, 2024, 44(11): 3446-3455.
Compd. | R. solani | F. graminearm | M.oryzae | S. sclerotiorm | S. rolfsii | C. camelliae |
---|---|---|---|---|---|---|
5a | 54.5±2.9 | 12.6±1.1 | — | 65.5±2.2 | 74.9±0.8 | 33.8±1.9 |
5b | 38.1±1.3 | 11.0±0.9 | — | 31.3±3.2 | 72.7±2.4 | 40.5±2.9 |
6a | 68.9±2.2 | 13.6±1.4 | 31.0±0.8 | 60.1±1.2 | 37.8±3.7 | 33.2±1.8 |
6b | 56.6±2.2 | 24.6±1.4 | 51.9±3.3 | 19.6±1.4 | 44.2±3.3 | 38.2±1.1 |
6c | 54.1±3.1 | 25.6±2.3 | 72.5±2.6 | 22.9±0.4 | 76.7±3.0 | 44.5±0.8 |
6d | 38.8±1.6 | 17.3±1.4 | 14.3±2.0 | 40.2±1.6 | 21.2±3.6 | 47.0±1.1 |
6e | 52.9±1.9 | 13.9±1.6 | — | 59.8±1.3 | 47.0±1.6 | 19.4±1.5 |
6f | 64.6±0.7 | 26.9±2.4 | 36.9±2.9 | 57.4±2.2 | 54.8±2.9 | 49.5±0.9 |
6g | 47.4±2.2 | 21.6±0.7 | 21.3±0.3 | 28.9±3.0 | 39.6±1.6 | 40.3±0.9 |
6h | 43.0±3.3 | 25.6±1.0 | 41.5±0.7 | 17.3±2.2 | 39.2±1.6 | 21.6±1.7 |
6i | 81.5±0.6 | 23.3±0.9 | 25.4±2.0 | 37.5±1.9 | 76.7±3.0 | 46.7±2.0 |
6j | 36.0±3.2 | 13.0±0.9 | 28.2±1.1 | 36.9±1.7 | 40.3±3.4 | 41.4±0.9 |
6k | 77.5±0.9 | 25.6±2.3 | 16.7±2.1 | 40.7±0.9 | 48.1±1.2 | 29.7±0.9 |
6l | 40.9±2.4 | 13.9±1.6 | 20.5±1.9 | 20.5±3.2 | 43.8±2.4 | 39.6±0.8 |
6m | 22.7±2.9 | 15.3±1.3 | 13.3±3.3 | 27.7±1.0 | — | 20.9±0.6 |
6n | 43.1±3.2 | 45.5±1.0 | — | 23.8±0.6 | 28.6±1.1 | 14.5±2.1 |
6o | 41.9±1.0 | 11.3±1.5 | — | 19.9±2.4 | 40.3±1.2 | 30.0±1.2 |
7a | 77.8±2.1 | 45.8±1.6 | 49.8±1.2 | 77.4±3.1 | 92.9±0.5 | 28.3±1.5 |
7b | 56.6±0.9 | 36.9±2.0 | 32.1±2.3 | 97.3±1.5 | 30.7±1.8 | 54.1±2.5 |
7c | 75.4±1.1 | 51.8±2.3 | 38.0±3.8 | 92.9±3.2 | 58.0±1.9 | 71.8±1.6 |
Hymexazol | 56.0±1.7 | 44.2±0.7 | 49.1±2.2 | 94.4±0.5 | 85.9±0.5 | 26.1±1.5 |
Compd. | R. solani | F. graminearm | M.oryzae | S. sclerotiorm | S. rolfsii | C. camelliae |
---|---|---|---|---|---|---|
5a | 54.5±2.9 | 12.6±1.1 | — | 65.5±2.2 | 74.9±0.8 | 33.8±1.9 |
5b | 38.1±1.3 | 11.0±0.9 | — | 31.3±3.2 | 72.7±2.4 | 40.5±2.9 |
6a | 68.9±2.2 | 13.6±1.4 | 31.0±0.8 | 60.1±1.2 | 37.8±3.7 | 33.2±1.8 |
6b | 56.6±2.2 | 24.6±1.4 | 51.9±3.3 | 19.6±1.4 | 44.2±3.3 | 38.2±1.1 |
6c | 54.1±3.1 | 25.6±2.3 | 72.5±2.6 | 22.9±0.4 | 76.7±3.0 | 44.5±0.8 |
6d | 38.8±1.6 | 17.3±1.4 | 14.3±2.0 | 40.2±1.6 | 21.2±3.6 | 47.0±1.1 |
6e | 52.9±1.9 | 13.9±1.6 | — | 59.8±1.3 | 47.0±1.6 | 19.4±1.5 |
6f | 64.6±0.7 | 26.9±2.4 | 36.9±2.9 | 57.4±2.2 | 54.8±2.9 | 49.5±0.9 |
6g | 47.4±2.2 | 21.6±0.7 | 21.3±0.3 | 28.9±3.0 | 39.6±1.6 | 40.3±0.9 |
6h | 43.0±3.3 | 25.6±1.0 | 41.5±0.7 | 17.3±2.2 | 39.2±1.6 | 21.6±1.7 |
6i | 81.5±0.6 | 23.3±0.9 | 25.4±2.0 | 37.5±1.9 | 76.7±3.0 | 46.7±2.0 |
6j | 36.0±3.2 | 13.0±0.9 | 28.2±1.1 | 36.9±1.7 | 40.3±3.4 | 41.4±0.9 |
6k | 77.5±0.9 | 25.6±2.3 | 16.7±2.1 | 40.7±0.9 | 48.1±1.2 | 29.7±0.9 |
6l | 40.9±2.4 | 13.9±1.6 | 20.5±1.9 | 20.5±3.2 | 43.8±2.4 | 39.6±0.8 |
6m | 22.7±2.9 | 15.3±1.3 | 13.3±3.3 | 27.7±1.0 | — | 20.9±0.6 |
6n | 43.1±3.2 | 45.5±1.0 | — | 23.8±0.6 | 28.6±1.1 | 14.5±2.1 |
6o | 41.9±1.0 | 11.3±1.5 | — | 19.9±2.4 | 40.3±1.2 | 30.0±1.2 |
7a | 77.8±2.1 | 45.8±1.6 | 49.8±1.2 | 77.4±3.1 | 92.9±0.5 | 28.3±1.5 |
7b | 56.6±0.9 | 36.9±2.0 | 32.1±2.3 | 97.3±1.5 | 30.7±1.8 | 54.1±2.5 |
7c | 75.4±1.1 | 51.8±2.3 | 38.0±3.8 | 92.9±3.2 | 58.0±1.9 | 71.8±1.6 |
Hymexazol | 56.0±1.7 | 44.2±0.7 | 49.1±2.2 | 94.4±0.5 | 85.9±0.5 | 26.1±1.5 |
Pathogenic fungi | Compd. | y=ax+b | EC50/(mg•L-1) | r |
---|---|---|---|---|
R. solani | 6i | y=2.6891+1.7718x | 20.15 | 0.9921 |
6k | y=2.2707+1.8132x | 32.01 | 0.9879 | |
7a | y=3.4966+1.3076x | 14.11 | 0.9910 | |
7c | y=4.8064+0.7520x | 1.81 | 0.9931 | |
Hymexazol | y=2.7947+1.3286x | 45.70 | 0.9862 | |
Carbendazim | y=3.1039+4.8877x | 1.09 | 0.9925 | |
S. sclerotiorm | 7a | y=3.5630+1.5302x | 8.69 | 0.9938 |
7b | y=4.1653+1.1322x | 5.46 | 0.9954 | |
7c | y=4.1114+1.5213x | 3.84 | 0.9909 | |
Hymexazol | y=3.7335+1.7243x | 5.43 | 0.9974 | |
S.rolfsii | 6c | y=2.9569+1.4651x | 24.80 | 0.9966 |
6i | y=2.9250+1.6167x | 19.21 | 0.9824 | |
7a | y=2.3327+1.9787x | 22.29 | 0.9989 | |
Hymexazol | y=4.0154+1.2877x | 5.82 | 0.9928 |
Pathogenic fungi | Compd. | y=ax+b | EC50/(mg•L-1) | r |
---|---|---|---|---|
R. solani | 6i | y=2.6891+1.7718x | 20.15 | 0.9921 |
6k | y=2.2707+1.8132x | 32.01 | 0.9879 | |
7a | y=3.4966+1.3076x | 14.11 | 0.9910 | |
7c | y=4.8064+0.7520x | 1.81 | 0.9931 | |
Hymexazol | y=2.7947+1.3286x | 45.70 | 0.9862 | |
Carbendazim | y=3.1039+4.8877x | 1.09 | 0.9925 | |
S. sclerotiorm | 7a | y=3.5630+1.5302x | 8.69 | 0.9938 |
7b | y=4.1653+1.1322x | 5.46 | 0.9954 | |
7c | y=4.1114+1.5213x | 3.84 | 0.9909 | |
Hymexazol | y=3.7335+1.7243x | 5.43 | 0.9974 | |
S.rolfsii | 6c | y=2.9569+1.4651x | 24.80 | 0.9966 |
6i | y=2.9250+1.6167x | 19.21 | 0.9824 | |
7a | y=2.3327+1.9787x | 22.29 | 0.9989 | |
Hymexazol | y=4.0154+1.2877x | 5.82 | 0.9928 |
Compd. | C. elegans | B. xylophilus | Compd. | C. elegans | B. xylophilus |
---|---|---|---|---|---|
5a | 41.8±2.6 | — | 6j | 25.5±3.2 | — |
5b | 44.4±2.8 | — | 6k | 41.5±2.7 | — |
6a | 95.2±1.8 | 93.6±0.9 | 6l | 38.1±3.2 | — |
6b | 25.9±3.0 | — | 6m | 20.3±3.8 | — |
6c | 97.0±2.7 | — | 6n | — | — |
6d | 27.3±1.4 | — | 6o | — | — |
6e | — | — | 7a | 27.5±1.8 | — |
6f | 16.8±1.4 | — | 7b | 13.2±2.7 | — |
6g | 41.8±2.4 | — | 7c | — | — |
6h | 86.6±2.3 | — | Fosthiazate | 56.1±2.8 | 74.4±2.1 |
6i | 43.9±2.2 | 38.7±2.4 | Fluopyram | 100.0±0.0 | 91.5±1.1 |
Compd. | C. elegans | B. xylophilus | Compd. | C. elegans | B. xylophilus |
---|---|---|---|---|---|
5a | 41.8±2.6 | — | 6j | 25.5±3.2 | — |
5b | 44.4±2.8 | — | 6k | 41.5±2.7 | — |
6a | 95.2±1.8 | 93.6±0.9 | 6l | 38.1±3.2 | — |
6b | 25.9±3.0 | — | 6m | 20.3±3.8 | — |
6c | 97.0±2.7 | — | 6n | — | — |
6d | 27.3±1.4 | — | 6o | — | — |
6e | — | — | 7a | 27.5±1.8 | — |
6f | 16.8±1.4 | — | 7b | 13.2±2.7 | — |
6g | 41.8±2.4 | — | 7c | — | — |
6h | 86.6±2.3 | — | Fosthiazate | 56.1±2.8 | 74.4±2.1 |
6i | 43.9±2.2 | 38.7±2.4 | Fluopyram | 100.0±0.0 | 91.5±1.1 |
Nematode | Compd. | y=ax+b | LC50/(mg•L-1) | 相关系数 |
---|---|---|---|---|
C. elegans | 6a | y=4.0275+1.6258x | 3.96 | 0.9953 |
6c | y=0.7434+3.3954x | 49.15 | 0.9743 | |
6h | y=0.7556+3.1950x | 63.31 | 0.9658 | |
Fosthiazate | y=0.8439+2.3630x | 57.39 | 0.9927 | |
Fluopyram | y=3.0776+2.8673x | 4.68 | 0.9740 | |
B. xylophilus | 6a | y=0.7617+2.4936x | 50.08 | 0.9888 |
Fosthiazate | y=2.7041+1.6489x | 24.68 | 0.9801 | |
Fluopyram | y=5.8004+3.3039x | 0.57 | 0.9953 |
Nematode | Compd. | y=ax+b | LC50/(mg•L-1) | 相关系数 |
---|---|---|---|---|
C. elegans | 6a | y=4.0275+1.6258x | 3.96 | 0.9953 |
6c | y=0.7434+3.3954x | 49.15 | 0.9743 | |
6h | y=0.7556+3.1950x | 63.31 | 0.9658 | |
Fosthiazate | y=0.8439+2.3630x | 57.39 | 0.9927 | |
Fluopyram | y=3.0776+2.8673x | 4.68 | 0.9740 | |
B. xylophilus | 6a | y=0.7617+2.4936x | 50.08 | 0.9888 |
Fosthiazate | y=2.7041+1.6489x | 24.68 | 0.9801 | |
Fluopyram | y=5.8004+3.3039x | 0.57 | 0.9953 |
[1] |
Hunt J. C.; Biggs E.; Clarke E. D.; Whitingham W. G. Bioorg. Med. Chem. Lett. 2007, 17, 5222.
|
[2] |
Migawa T. M.; Townsend B. L. J. Org. Chem. 2001, 66, 4776.
pmid: 11442403 |
[3] |
Migawa T. M.; Drach J. C.; Townsend B. L. J. Med. Chem. 2005, 48, 3840.
|
[4] |
Wang G. L.; Chen X.; Chang Y. N.; Du D.; Li Z.; Xu X. Y. Chin. Chem. Lett. 2015, 26, 1502.
|
[5] |
Gadekar S. M.; Ross E. J. Org. Chem. 1961, 26, 613.
|
[6] |
Gadekar S. M.; Frederick J. L. J. Org. Chem. 1962, 27, 1383.
|
[7] |
Caliendo G.; Fiorino F.; Grieco P.; Prissutti E.; Santagada V.; Meli R.; Raso G. M.; Zanesco A.; Nucci G. D. Eur. J. Med. Chem. 1999, 34, 1043.
|
[8] |
Van Heyningen E. J. Am. Chem. Soc. 1955, 77, 6562.
|
[9] |
Wang G. L.; Chen X, L.; Deng Y, Y.; Li Z.; Xu X, Y. J. Agric. Food Chem. 2015, 63, 6883.
|
[10] |
Zhang J.-P.; Li P.; Wang Y.-H.; Zhang C.; Chen L.-J.; Tang X.; He. M.; Xue W. Chem. J. Chin Univ. 2018, 39, 1455 (in Chinese).
|
(张菊平, 李普, 王一会, 张橙, 陈丽娟, 汤旭, 贺鸣, 薛伟, 高等学校化学学报, 2018, 39, 1455.)
doi: 10.7503/cjcu20170785 |
|
[11] |
Zhang Y.; Zhu H.-W.; Shang J.-F.; Wang B.-L.; Li Z.-M. Chin. J. Org. Chem. 2019, 39, 86 (in Chinese).
|
(张燕, 朱洪伟, 尚俊峰, 王宝雷, 李正名, 有机化学, 2019, 39, 86.)
|
|
[12] |
Chen D. C.; Yang H. P.; Li Z.; Maienfischa P.; Xu X. Y. J. Mol. Struct. 2022, 1264.
|
[13] |
Duan Z.-F.; Shao L. Chin. J. Org. Chem. 2015, 35, 2004 (in Chinese).
|
(段志芳, 邵玲, 有机化学, 2015, 35, 2004.)
doi: 10.6023/cjoc201502028 |
|
[14] |
Song B. A. CN 106432125, 2017.
|
[15] |
Chen J. X.; Gan X. H.; Yi C. F.; Wang S. B.; Yang Y. Y.; He F. C.; Hu D.Y.; Song B. A. Chin. J. Chem. 2018, 36, 939.
|
[16] |
Gupta R.; Sirohi R.; Kishore D. Chem. Incl. Med. Chem. 2006, 45, 2147.
|
[17] |
El Rayes S. M.; Ali I. A. I.; Fathalla W.; Mahmoud M. A. A. ACS Omega. 2020, 5, 6781.
|
[18] |
Chen X.-W. M.S. Thesis, Guizhou University, Guiyang, 2016 (in Chinese).
|
(陈学文, 硕士论文, 贵州大学, 贵阳, 2016.)
|
|
[19] |
Chen X.-W.; Gan X.-H.; Chen J.-X.; Chen Y.-Z.; Wang Y.-J.; Hu D.-Y.; Song B.-A. Chin. J. Org. Chem. 2017, 37, 2343 (in Chinese).
|
(陈学文, 甘秀海, 陈吉祥, 陈永中, 王艳娇, 胡德禹, 宋宝安, 有机化学, 2017, 37, 2343.)
doi: 10.6023/cjoc201703022 |
|
[20] |
Chen J. X.; Luo Y, Q. Pest Manage. Sci. 2020, 76, 3188.
|
[21] |
Shi J.-C. M.S. Thesis, Yangtze University, Jingzhou, 2023 (in Chinese).
|
(时锦超, 硕士论文, 长江大学, 荆州, 2023.)
|
|
[22] |
Kang Z.; Gu B.-G. Standard Operating Procedures for Bioactivity Testing of Pesticides——Fungicide Roll, Chemical Industry Press, Shenyang, 2016, pp. 155-156 (in Chinese).
|
(康卓, 顾宝根, 农药生物活性测试标准操作规范——杀菌剂卷, 化工出版社, 沈阳, 2016, pp. 155-156.)
|
|
[23] |
Zhou P.; Huang J.-J.; He C.-W.; Guo Q.-N.; You J.; Liu Y.-F.; Xu Z.-H. Chin. J. Pestic. Sci. 2022, 24, 1367 (in Chinese).
|
(周蒲, 黄俊杰, 何昌文, 郭倩男, 游江, 刘一凡, 徐志红, 农药学学报, 2022, 24, 1367.)
|
[1] | Zhilan Yu, Zhiling Zou, Zhiwen Yuan, Chunling Zeng, Lifen Peng, Xinhua Xu, Zilong Tang, Xirong Liu. Sulfuryl Group-Involved Drugs Approved by the Food and Drug Administration (FDA) from 2021 to 2023 [J]. Chinese Journal of Organic Chemistry, 2024, 44(9): 2682-2699. |
[2] | Mengjin Liu, Yan Xiao, Kai Zhou, Zicheng Li, Wencai Huang. Synthesis of 3,5-Diaryl-1,2,4-oxadiazole by One-Pot Homocoupling Reaction [J]. Chinese Journal of Organic Chemistry, 2024, 44(7): 2251-2256. |
[3] | Dianfan Liu, Jianzhi Wang, Mengqing Wang, Xiaobei Chen, Yanwei Hu, Shilei Zhang. o-Iodoarylation of Thiols Enabled by Aryne Generated from o-Diiodoarene and Sodium Hydride [J]. Chinese Journal of Organic Chemistry, 2024, 44(7): 2363-2370. |
[4] | Jiayi Liang, Yaqi Yang, Jianping Liu, Qing Xu, Libiao Han. Sodium Halides-Promoted S—Si Bond Activation and Its Application in the Synthesis of Unsymmetrical Thioethers [J]. Chinese Journal of Organic Chemistry, 2024, 44(5): 1658-1666. |
[5] | Qiannan Guo, Sen Huang, Wei Zhao, Wei Zhao, Yue Yan, Jihai Wang, Zhihong Xu. Design, Synthesis and Nematicidal and Fungicidal Activities of 8-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine Oxadiazole Thioether Derivatives [J]. Chinese Journal of Organic Chemistry, 2024, 44(5): 1620-1629. |
[6] | Penghui Li, Qingyang Xie, Fuxian Wan, Yuanhong Zhang, Lin Jiang. Synthesis and Fungicidal Activity of Novel Substituted Pyrimidine-5-carboxamides Bearing Cyclopropyl Moiety [J]. Chinese Journal of Organic Chemistry, 2024, 44(2): 650-656. |
[7] | Wenwen Chen, Qin Zhang, Songyue Zhang, Fangfang Huang, Xinyin Zhang, Jianfeng Jia. Visible Light Promoted Coupling Reaction of Alkynyl Iodide and Sodium Sulphinate without Photocatalyst [J]. Chinese Journal of Organic Chemistry, 2024, 44(2): 584-592. |
[8] | Lingna Wang, Xiaoqing Liu, Gang Lin, Hongying Jin, Minjun Jiao, Xuefen Liu, Shuping Luo. Photocatalytic Activation of C(sp3)—H Bonds to Form C—S Bonds Catalyzed by (Oxybis(4,1-phenylene))bis(phenylmethanone) [J]. Chinese Journal of Organic Chemistry, 2023, 43(8): 2848-2854. |
[9] | Feng Wang, Yu Chen, Hongyan Pei, Jing Zhang, Lixin Zhang. Design, Synthesis and Antifungal Activities of Novel 1,2,4-Oxadiazole Derivatives Containing Piperidine [J]. Chinese Journal of Organic Chemistry, 2023, 43(8): 2826-2836. |
[10] | Min Liu, Dongyan Yang, Yumei Xiao, Wangcang Su, Fenghai Zhao, Qin Zhaohai .. Synthesis and Bioactivities of 5-Nitroimino-[1,4-2H]-1,2,4-triazolines as Olefin-Imidacloprid Mimics [J]. Chinese Journal of Organic Chemistry, 2023, 43(8): 2790-2799. |
[11] | Xuedan Wu, Ruixiang Xu, Xiaolong Fang, Kehua Zhang, Jie Jin. Design and Synthesis of N-Tetrazole and N-Oxadiazole Heterocyclic Derivatives of Sinomenine [J]. Chinese Journal of Organic Chemistry, 2023, 43(7): 2506-2518. |
[12] | Xiantao Ma, Xiaoyu Yan, Yingying Zhu, Shuanglin Niu, Yuxuan Wang, Chao Yuan. Water-Promoted Green Synthesis of Heteroaryl Thioether [J]. Chinese Journal of Organic Chemistry, 2023, 43(6): 2136-2142. |
[13] | Jiamin Ma, Jiaoxiong Li, Qiansen Meng, Xianghua Zeng. Advances on the Radical Sulfonation of Alkynes [J]. Chinese Journal of Organic Chemistry, 2023, 43(6): 2040-2052. |
[14] | Yang Sun, Yang Wang, Zichan Zhang, Ye Qian, Guicheng Luo, Beibei Zhou, Lisha Miao, Yudie Chen, Hong Dai, Baolin Xu, Zhengguang Wu. Synthesis and Bioactivities of Novel Pyrazole Oxime Derivatives Containing 1,3,4-Oxadiazole Group [J]. Chinese Journal of Organic Chemistry, 2023, 43(4): 1584-1590. |
[15] | Chunyang Liu, Yan Li, Qian Zhang. Copper-Catalyzed Allylic C(sp3)—H Sulfonylation of Cyclic Olefins [J]. Chinese Journal of Organic Chemistry, 2023, 43(3): 1091-1101. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||