首页> 外国专利> 1-ETHYL-6- NITRO-7- (4-METHYLPIPERAZINYL)- 4-OXO- 1,4-DIHYDROQUINOLINE -3-CARBOXYLIC ACID OR ITS HYDROCHLORIDE SHOWING ANTIBACTERIAL ACTIVITY

1-ETHYL-6- NITRO-7- (4-METHYLPIPERAZINYL)- 4-OXO- 1,4-DIHYDROQUINOLINE -3-CARBOXYLIC ACID OR ITS HYDROCHLORIDE SHOWING ANTIBACTERIAL ACTIVITY

机译:1-乙基-6-硝基-7-(4-甲基哌嗪基)-4-OXO- 1,4-二氢喹啉-3-羧酸或其盐显示的抗菌活性

摘要

FIELD: organic chemistry. SUBSTANCE: synthesis is carried out by boiling of 1-ethyl- 6-nitro-7 -chloro-4-oxo-1,4 -dihydroquinoline-3-carboxylic acid ethyl ester in HCl medium in the presence of CH3COOH following by isolation of corresponding acid and treatment with N-methylpiperazine at boiling in dimethylformamide medium. Yield is 72%, m. p. is 242-243 C, empirical formula is C17H20N4O5. Prepared product is conversed to hydrochloride by treatment with HCl spirituous solution. Yield is 96%, m. p. is 261-262 C, empirical formula is C17H20N4O5HCl. Synthesized product shows antibacterial action against gram-positive, gram-negative bacteria, pathogenic fungi, pathogens of microsporia, trichophytosis, candidosis. Maximal tolerant dose is 0.5-1.25 mcg/ml, toxicity LD50 = 2000 mg/kg (for С17H20N4O5) and 1000 mg/kg (for C17H2N4O8HCl). EFFECT: increased effectiveness of products, improved method of synthesis. 1 dwg, 7 tbl
机译:领域:有机化学。物质:通过将1-乙基-6-硝基-7-氯-4-氧代-1,4-二氢喹啉-3-羧酸乙酯在HCl介质中,在CH 3的存在下沸腾进行合成通过分离相应的酸并在二甲基甲酰胺介质中在沸腾下用N-甲基哌嗪处理来处理。产率为72%,m。 p。是242-243 C,经验公式是C 17 H 20 N 4 O 5 。通过用HCl溶剂溶液处理,将制备的产物转化为盐酸盐。产率为96%,m。 p。是261-262 C,经验公式是C 17 H 20 N 4 O 5 HCl。合成产物对革兰氏阳性,革兰氏阴性细菌,病原真菌,小孢子菌病原体,毛癣菌病,念珠菌病表现出抗菌作用。最大耐受剂量为0.5-1.25 mcg / ml,毒性LD 50 = 2000 mg / kg(对于С 17 H 20 N 4 O 5 )和1000 mg / kg(对于C 17 H 2 N 4 O 8 HCl)。效果:提高产品功效,改进合成方法。 1桶,7桶

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