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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, analgesic, anti-inflammatory, ulcerogenic index and antibacterial activities of novel 2-methylthio-3-substituted-5,6,7,8-tetrahydrobenzo (b) thieno(2,3-d)pyrimidin-4(3H)-ones.
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Synthesis, analgesic, anti-inflammatory, ulcerogenic index and antibacterial activities of novel 2-methylthio-3-substituted-5,6,7,8-tetrahydrobenzo (b) thieno(2,3-d)pyrimidin-4(3H)-ones.

机译:新型2-甲硫基-3-取代的5,6,7,8-四氢苯并(b)噻吩并(2,3-d)嘧啶-4(3H)-的合成,镇痛,抗炎,促溃疡指数和抗菌活性那些。

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摘要

A variety of novel 2-methylthio-3-substituted-5,6,7,8-tetrahydrobenzo (b) thieno[2,3-d]pyrimidin-4(3H)-ones have been synthesized by reacting (2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo (b) thieno[2,3-d]pyrimidin-3-yl)dithiocarbamic acid methyl ester (5) with a variety of amines. The starting material dithiocarbamate (5) was synthesized from 2-amino-3-carbethoxy-4,5,6,7-tetrahydrobenzo (b) thiophene (1) by a novel innovative route. The title compounds were investigated for analgesic, anti-inflammatory, ulcerogenicity index and antibacterial activities. While the test compounds exhibited significant activity, the compounds 1-methyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo (b) thieno[2,3-d]pyrimidin-3-yl)thiourea (A1), 1-dimethyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo (b) thieno[2,3-d]pyrimidin-3-yl)thiourea (A2), 1-diethyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo (b) thieno[2,3-d]pyrimidin-3-yl)thiourea (A3) and 1-pyrrolidinyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo(b) thieno[2,3-d]pyrimidin-3-yl)thiourea (A4) showed more potent analgesic activity and the compounds 1-dimethyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo (b) thieno[2,3-d]pyrimidin-3-yl)thiourea (A2), 1-diethyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo (b) thieno-[2,3-d]pyrimidin-3-yl)thiourea (A3) and 1-pyrrolidinyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo (b) thieno[2,3-d] pyrimidin-3-yl)thiourea (A4) showed more potent anti-inflammatory activity than the reference standard diclofenac sodium.
机译:各种新型的2-甲硫基-3-取代的5,6,7,8-四氢苯并(b)噻吩并[2,3-d]嘧啶-4(3H)-已通过(2-甲硫基- 4-氧代-3H-5,6,7,8-四氢苯并(b)噻吩并[2,3-d]嘧啶-3-基)二硫代氨基甲酸甲酯(5)与多种胺。起始原料二硫代氨基甲酸酯(5)是由2-氨基-3-甲乙氧基-4,5,6,7-四氢苯并(b)噻吩(1)合成的。研究了标题化合物的镇痛,抗炎,致溃疡指数和抗菌活性。尽管受试化合物显示出显着的活性,但化合物1-甲基-3-(2-甲硫基-4-氧代-3H-5,6,7,8-四氢苯并(b)噻吩并[2,3-d]嘧啶-3 -基)硫脲(A1),1-二甲基-3-(2-甲硫基-4-氧代-3H-5,6,7,8-四氢苯并(b)噻吩并[2,3-d]嘧啶-3-基)硫脲(A2),1-二乙基-3-(2-甲硫基-4-氧代-3H-5,6,7,8-四氢苯并(b)噻吩并[2,3-d]嘧啶-3-基)硫脲(A3)和1-pyrrolidinyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo(b)thieno [2,3-d] pyrimidin-3-yl)thiourea(A4 )显示出更强的镇痛活性,化合物1-二甲基-3-(2-甲硫基-4-氧代-3H-5,6,7,8-四氢苯并(b)噻吩并[2,3-d]嘧啶-3- yl)thiourea(A2),1-diethyl-3-(2-methylthio-4-oxo-3H-5,6,7,8-tetrahydrobenzo(b)thieno- [2,3-d] pyrimidin-3-yl )硫脲(A3)和1-吡咯烷基-3-(2-甲硫基-4-氧代-3H-5,6,7,8-四氢苯并(b)噻吩并[2,3-d]嘧啶-3-基)硫脲(A4)显示比参考标准双氯芬酸钠更有效的抗炎活性。

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