首页> 外国专利> 1,1'-DIGLYCIDYL-3,3'-DIETHYLBIS-(1,2,4-TRIAZOLE-5-ONE-4-YL)- -METHANE SHOWING ANTITUMOR ACTIVITY AND 3,3'-DIETHYLBIS-(1,2,4-TRIAZOLE-5-ONE-4-YL)-METHANE AS AN INTERMEDIATE COMPOUND FOR SYNTHESIS OF 1,1'-DIGLYCIDYL-3,3'-DIETHYLBIS-(1,2,4-TRIAZOLE-5-ONE-4-YL)- -METHANE

1,1'-DIGLYCIDYL-3,3'-DIETHYLBIS-(1,2,4-TRIAZOLE-5-ONE-4-YL)- -METHANE SHOWING ANTITUMOR ACTIVITY AND 3,3'-DIETHYLBIS-(1,2,4-TRIAZOLE-5-ONE-4-YL)-METHANE AS AN INTERMEDIATE COMPOUND FOR SYNTHESIS OF 1,1'-DIGLYCIDYL-3,3'-DIETHYLBIS-(1,2,4-TRIAZOLE-5-ONE-4-YL)- -METHANE

机译:1,1'-二乙二醇-3,3'-二乙基-(1,2,4-三唑-5-一-4-基)-甲氧基显示抗张活性和3,3'-二乙基-(1,2, 4-三唑-5-一-4-基)-甲烷作为合成1,1'-二糖基-3,3'-二乙基-(1,2,4-三唑-5-ONE-4-的中间体) YL)--甲烷

摘要

FIELD: organic chemistry. SUBSTANCE: product: derivatives of triazole, in part, 1,1'-diglycidyl-3,3'-diethyl- -bis(1,2,4-triazole-5-one-4-yl)-methane and 3,3'-diethylbis- -(1,2,4-triazole-5-one-4-yl)-methane as semiproduct. a) Synthesis of semiproduct is carried out from urea and hydrazine hydrate followed by acylation with propionic anhydride and cyclization of the synthesized semicarbazone in an aqueous alkali to 3-ethyltrazole-5-one that is treated with paraform in acid medium. b) Synthesized semiproduct is alkylated with epichlorohydrin. Yield, %; m. p., C; empirical formula: a) 28, 2970298, C9H12N6O2; b) 43, 119-121, C15H20N6O4. Toxicity of new substance is less for about 10 times as compared with 1,2,4-triglycidylurazole and it can be used at doses below 100 mg/kg in order to inhibit the growth of Jensen sarcoma, Walker carcinosarcoma and Sarcoma M-1 by 94; 92 and 72% as compared with 59; 60 and 20%, respectively. EFFECT: improved method of synthesis, enhanced antitumor activity. 2 cl, 3 tbl
机译:领域:有机化学。物质:产品:三唑的衍生物,部分为1,1'-二缩水甘油基-3,3'-二乙基-双(1,2,4-三唑-5-一-4-基)-甲烷和3,3 '-二乙基双--(1,2,4-三唑-5-一-4-基)-甲烷为半产物。 a)从尿素和水合肼进行半产物的合成,然后用丙酸酐酰化,并将合成的半脲在碱水溶液中环化成3-乙基三唑-5-酮,在酸性介质中用对羟基苯甲酸酯处理。 b)用表氯醇烷基化合成的半产物。产量, %;米p。,C;经验公式:a)28、2970298,C 9 H 12 N 6 O 2 ; b)43,119-121,C 15 H 20 N 6 O 4 。与1,2,4-三缩水甘油基尿嘧啶相比,新物质的毒性要低约10倍,并且可以以低于100 mg / kg的剂量使用,以抑制Jensen肉瘤,Walker癌肉瘤和肉瘤M-1的生长。 94; 92%和72%,而59%; 60%和20%。效果:改进的合成方法,增强的抗肿瘤活性。 2厘升,3汤匙

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