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1)  thiazolidonyl
噻唑烷酮基
2)  4-oxo-thiazolidine
4-羰基噻唑烷酮
3)  thiazolidone
噻唑烷酮
1.
Five N tetrahydrobenzothiazolyl imines have been synthesized by the condensation of 4,5,6,7 tetrahydro 2 benzothiazolamine with aromatic aldehydes and the reactions of imines respectively, with thioglycollic acid obtained five thiazolidones.
2-氨基四氢苯并噻唑和芳香醛进行缩合反应,合成了5个N-四氢苯并噻唑亚胺化合物,它们分别与巯基乙酸反应制备了5个4-噻唑烷酮。
2.
According to the principle of superposition activity, in this article, we have synthesized a series of thiazolidone and acylthiourea derivatives which are not reported in the literature by introducting 1,2,3-triazole-based, 1,3,4–thiadiazole and dibenzo into acetyl-hydroxy acyl thiazolidoneand thiourea derivatives through the promotion of ultrasonic radiation.
噻唑烷酮类化合物具有重要生理活性,可作杀菌剂、放射线增感剂、抗高血压和糖尿病的药物。
4)  thiazolidinedione
噻唑烷二酮
1.
Synthesis of Coumarin-thiazolidinediones;
香豆素噻唑烷二酮类化合物的合成
2.
According to the latest information from the 41~(th) EASD Annual Meeting in 2005,we summarize some noval therapeutic drugs for diabetes,such as non-thiazolidinedione insulin sensitizer incretins,DPP-IV inhibitors,new insulin analogue.
结合2005年欧洲糖尿病年会的最新信息,对近年来已上市和正在试验及研发阶段的新型降糖药物,如非噻唑烷二酮类胰岛素增敏剂、肠促胰岛素、DPP-Ⅳ抑制剂、新型胰岛素类似物等进行综述。
3.
AIM To build a model of two series of PPARγ agonists thiazolidinedione and aryketo-acid derivatives using 3D-QSAR method, and to reveal the structural features affecting the binding activity to PPARγ, which relates to antihyperglycemic and antihyperlipidemic activity and has a potential application to the treatment of type II diabetes.
目的 建立PPARγ激动剂 噻唑烷二酮和芳酮酸类化合物的三维定量构效关系 ,为设计高活性PPARγ激动剂提供结构信息。
5)  2-thiazolidinone
2-噻唑烷酮
1.
Fosthiazate was synthesized by condensing 2-thiazolidinone with O,O'-diethylthio- phosphonochloride,and then alkylating the resulting O,O'- diethyl-2-oxo-1,3-thiazolidine-3-thiophosphate with dimethylamine, followedby direct alkylation of the ammonium salt with 2-bromobutane.
先将2-噻唑烷酮与O,O'-二乙基硫代磷酰氯进行缩合反应生成O,O'-二乙基-2-氧代-1,3-噻唑烷-3-基硫逐磷酸酯,该硫逐磷酸酯再与二甲胺反应生成相应硫代磷酸酯铵盐,然后与溴代仲丁烷进行烷基化反应得到噻唑磷。
2.
Fosthiazate was synthesized by reacting phosphorus trichloride with S-sec-butyl disulfide and then condensing with 2-thiazolidinone.
介绍了以三氯化磷、仲丁基二硫化物为原料反应得到O-乙基-S-仲丁基硫代磷酰氯,再与2-噻唑烷酮缩合得到噻唑磷的合成方法。
3.
Its yield of 2-thiazolidinone came up to 82%.
以2-噻唑硫酮为原料,双氧水为氧化剂,醇钠为催化剂,合成2-噻唑烷酮。
6)  2-thiazolidinethione
2-噻唑烷酮
1.
2-Thiazolidinone was synthesized by the exchange reaction between the oxygen of chloroethanol and sulphur atom of 2-thiazolidinethione.
2-噻唑烷酮不仅是一个有用的中间体,而且其本身也具有一定的杀菌活性。
2.
Thiazolidone is synthesized by 2-thiazolidinethione and hydrogen peroxide.
本文以2-噻唑硫酮为原料,双氧水为氧化剂,对2-噻唑烷酮的合成进行了探索性研究,并将其工艺条件进一步优化,使反应收率达60%。
补充资料:3-乙基-2-硫代-4-噻唑烷二酮
CAS:   7648-01-3
分子式:  C5H7NOS2
分子质量: 161.23
沸点:   127℃(4 t
熔点:   35-39℃
中文名称: 3-乙基-2-硫代-4-噻唑烷二酮;N-乙基绕丹宁

英文名称: 3-ethyl-2-thioxo-4-Thiazolidinone;3-ethyl-rhodanin;3-ethylrodanin;3-ethyl-2-thioxo-4-thiazolidinon;3-ethvlrhodanine;4-Thiazolidinone,3-ethyl-2-thioxo-
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