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PROCESS FOR THE PREPARATION OF S-TRIAZOLO(3,4-B)BENZOTHIAZOLES

机译:S-三唑(3,4-B)苯并噻唑的制备方法

摘要

Title compds. (I; R = hydrogen, C1-11 alkyl, cyclopropyl, trifluoromethyl, R1 = H, Br, C1, or F; R2, R3 = C1-2 alkyl, C1-3 alkoxy, Br, C1, F or trifluoromethyl) were prepod. by reaction of 1acyl-4-(o-halophenyl)-3-thiosemicarbazide with base in the presence of anhydrous amide solvent. Thus, 2.4g 1-acetyl-4-(2-chlorophenyl) thiosemicarbazide was melted with 50ml DMF under N and added with 0.5g sodium hydride followed by refluxing for 126 hr to give 400mg 3-methyl-S-thiazole [3,4-b benzothiazole.
机译:标题内容。 (I; R =氢,C1-11烷基,环丙基,三氟甲基,R1 = H,Br,C1或F; R2,R3 = C1-2烷基,C1-3烷氧基,Br,C1,F或三氟甲基)前脚。 1酰基4-(邻卤代苯基)-3-硫代氨基脲在无水酰胺溶剂存在下与碱反应的方法。因此,在氮气气氛下,将2.4g 1-乙酰基-4-(2-氯苯基)硫代氨基脲与50ml DMF熔融,并加入0.5g氢化钠,然后回流126小时,得到400mg 3-甲基-S-噻唑[3,4]。 -b苯并噻唑。

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