CAS: 288-92-6; 1,2,4-Thiadiazole

该化合物是五种由五人组成的环状结构中含有两个氮原子和一个硫原子的杂交循环化合物,其特点是其芳香性质,有助于其稳定性和反应性;该化合物一般看起来无色,可视其形态和纯度,淡黄色液体或固体. 1,2,4-Thiadiazole因其在医药,农用化学品和材料科学方面的多种应用而闻名,因为它能够作为各种化学合成的建筑块.它表现出中度极性,影响其有机溶剂中的溶解性.由于该环状中氮和硫原子的存在,增加了其形成与金属协调综合体的潜力,使其对协调化学具有兴趣.此外,1,2,4-三硝胺衍生物往往显示生物活动,包括抗微生物和抗硫酸特性,从而进一步扩大其在医药化学中的用途.安全考虑,以及许多六环化合物,因为具有潜在的毒性和环境影响.

结构式图片

MSDS等安全信息

    上下游产品

    5-bromo-1,2,4-thiadiazole

    合成工艺路线路线简述

      📜5-溴-1,2,4-噻二唑置于甲醇,镍,三乙胺体系中,化学反应生成1,2,4-噻二唑
      参考文献:Goerdeler Et Al.,Chemische Berichte,1956,Vol. 89,P. 1534,1540
      标题:Goerdeler Et Al.,Chemische Berichte,1956,Vol. 89,P. 1534,1540

      专利信息


      专利号:US-10711138-B2
      优先权日:2016-04-08
      标题:Intermediates and procedures for the synthesis of functional materials
      发明人:KIRSCH PEER; GUNST SUSANN
      权利人:MERCK PATENT GMBH
      摘要:The present invention relates to heteroaromatic compounds which have two different reactive groups, their use in the synthesis of asymmetrically substituted compounds, and synthesis processes in which the compounds according to the invention are reacted sequentially with two different compounds, whereby an asymmetrically substituted compound is formed.

      专利号:US-12162849-B2
      优先权日:2018-12-21
      标题 :Synthesis of 3-methyl-1,2,4-thiadiazole-5-carbohydrazide or of the methyl-d3 deuterated form thereof
      发明人:HOVEYDA HAMID; DUTHEUIL GUILLAUME
      权利人:OGEDA SA
      摘要:The present invention relates to a method of synthesis of compound (I), wherein R1 represents methyl or methyl-d3, thus corresponding to 3-methyl-1,2,4-thiadiazole-5-carbohydrazide or to the methyl-d3 deuterated form thereof. These compounds are useful as key intermediates in the synthesis of pharmaceutical compounds, especially fezolinetant and deuterated fezolinetant.

      专利号:US-2003162992-A1
      优先权日:2001-12-14
      标 题 :Preparation of intermediates useful in the synthesis of antiviral nucleosides
      发明人:WATANABE KYOICHI A; DU JINFA
      摘要:The present invention is an efficient process for the manufacture of α-acyloxyacetaldehyde, a key intermediate in the synthesis of 1,3-oxathiolane and 1,3-dioxolane nucleosides.

      专利号:US-7138526-B1
      优先权日:1999-06-15
      标 题 :Solid phase synthesis of n,n-disubstituted diazacycloalkylcarboxy derivatives
      发明人:HERPIN TIMOTHY F; MORTON GEORGE C; SALVINO JOSEPH M
      权利人:AVENTIS PHARMA INC
      摘要:A method for the solid phase synthesis of N,N-disubstituted diazacycloalkylcarboxy derivatives of general formula (I) and (II) is claimed. Examples include piperazine-2-carboxamide. The method is applicable to the synthesis or large combinatorial libraries

      专利号:US-10981922-B2
      优先权日:2012-04-26
      标题 :Synthesis of lactams
      发明人:TAVARES FRANCIS XAVIER
      权利人:TAVARES FRANCIS XAVIER
      摘要:Methods for the synthesis of lactams are presented whereby a carboxylic acid of the formula HOOC—OR—NH-LG, wherein OR is an organic moiety and LG is a leaving group, is reacted with an acid, such as an organic acid, in particular a strong acid, and a dehydrating agent, which may be one in the same such as a strong acid anhydride, such that the amount of acid added allows for the desired transformation to take place without the loss of the leaving group (LG) before the cyclization, and recovering the lactam.

      专利号:US-6127515-A
      优先权日:1997-11-18
      标 题:Functionalized resin for the synthesis of amides and peptides
      发明人:MANFRE FRANCO; VANASSE BENOIT J; LABAUDINIERE RICHARD F; MORTON GEORGE C
      权利人:AVENTIS PHARM PROD INC
      摘要:This invention is directed to a functionalized amino resin of formula ##STR1## wherein S is a solid support; R is H or alkyl; A is ##STR2## Y is OH or OCOR 1 ; and R 1 is aliphatic or aromatic which is useful for the solid phase synthesis of amides, peptides and hydroxamic acids.

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      📌 第三方产品分析报告

      ✅ COA系统入驻 | 共享模式

      合成参考文献


      参考文献:10.1002/chem.200501528
      摘要:Bowman WR, Burchell CJ, Kilian P, Slawin AMZ, Wormald P, Woollins JD. Investigations on Organo–Sulfur–Nitrogen Rings and the Thiocyanogen Polymer, (SCN)x. Chemistry A European J. 2006 Aug 03;12(24):6366–81. doi: 10.1002/chem.200501528.
      参考文献:10.1007/s00894-014-2254-0
      摘要:Vega-Teijido MA, El Chamy Maluf S, Bonturi CR, Sambrano JR, Ventura ON. Theoretical insight into the mechanism for the inhibition of the cysteine protease cathepsin B by 1,2,4-thiadiazole derivatives. Journal of Molecular Modeling. 2014 Jun 01;20(6):2254. doi: 10.1007/s00894-014-2254-0.
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