📜2,4,5-三氯苯酚置于sodium Hydroxide,Potassium Carbonate体系中,用 水,丙酮 用作溶剂,化学反应 11.25H,反应生成2,4,5-T 甲酯 参考文献:Basic Amides Of 2,4,5-Trichlorophenoxyacetic,2,4,6-Trimethylphenoxyacetic And 4-Bromo-3,5-Dimethylphenoxyacetic Acid And Some Related Compounds; Synthesis And Pharmacological Screening 标题:Basic Amides Of 2,4,5-Trichlorophenoxyacetic,2,4,6-Trimethylphenoxyacetic And 4-Bromo-3,5-Dimethylphenoxyacetic Acid And Some Related Compounds; Synthesis And Pharmacological Screening 摘要:甲酯类化合物 Ii 的反应与 2,4,5-三氯苯氧乙酸 (Ia),2,4,6-三甲基苯氧乙酸 (Ib) 和 4-溴-3,5-二甲基苯氧乙酸 (Ic) 在沸腾的乙醇中与 2-二乙胺基乙胺,2-吗啉基乙胺,3-吗啉基丙胺,1-甲基哌嗪,3-(4-甲基哌嗪基)丙胺,3-[4-(2-甲苯基)哌嗪]丙胺和 1,4-双(3-氨基丙基)哌嗪的反应产生了基本酰胺 Va-Xic,这些酰胺以盐酸盐的形式分离出来.酸氯化物 Iva 和 Ivb 与 1,4-双(2-羟乙基)哌嗪和 1,4-双(3-羟丙基)哌嗪在二甲基甲酰胺中的反应直接产生了双酯的二盐酸盐 Xiiab 和 Xiiiab.制备的化合物仅具有微弱的中枢神经系统效应(主要是抑制性的);它们具有局部麻醉,轻度降压(其中一些为肾上腺素受体拮抗剂),抗心律失常和外周血管扩张活性. Doi:10.1135/cccc19831089
参考标题:Synthesis Of 5-Membered Heterocycles And Related Compounds. 作者:Vishnuji Ram,Hridvanand Pandey 摘要:Some 1-(2, 4-Dichlorophenoxy And 2, 4, 5-Trichlorophenoxy) Acetyl-4-Arylthiosemicarbazides Were Prepared From Corresponding Chlorophenoxyacetohydrazide. The Resulting Thiosemicarbazides Were Cyclised Into 1, 3, 4-Thiadiazoles And 5-Mercapto-1, 2, 4-Triazoles Under Different Reaction Conditions. The Mercapto Compounds Were Converted Into Sulphides And Sulphones. N'-Arylidene (2, 4-Dichlorophenoxy) Acetohydrazides And 5-Substituted-1, 3, 4-Oxadiazole-2-Thiones Were Also Prepared From (2, 4-Dichlorophenoxy And 2, 4, 5-Trichlorophenoxy) Acetohydrazides Separately And Were Subjected To Mannich Reaction. Some Of These Compounds Were Evaluated As Fungicides Against Aspergillus Niger.
合成参考文献
参考文献:10.1038/ncb3255 摘要:Lin R, Elf S, Shan C, Kang HB, Ji Q, Zhou L, Hitosugi T, Zhang L, Zhang S, Seo JH, Xie J, Tucker M, Gu TL, Sudderth J, Jiang L, Mitsche M, DeBerardinis RJ, Wu S, Li Y, Mao H, Chen PR, Wang D, Chen GZ, Hurwitz SJ, Lonial S, Arellano ML, Khoury HJ, Khuri FR, Lee BH, Lei Q, Brat DJ, Ye K, Boggon TJ, He C, Kang S, Fan J, Chen J. 6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling. Nat Cell Biol. 2015 Nov;17(11):1484–96.