合成目标产物 2,3-Dichlorophenyl Isothiocyanate 主要起始原料 Thiophosgene And 2,3-Dichloroaniline
(文献来源)合成步骤主要原料 Thiophosgene 和 2,3-Dichloroaniline
📜氯甲酸乙酯置于三乙胺体系中,化学反应生成 2,3-二氯苯基硫代异氰酸酯 参考文献:Compounds With Copper-Or Zinc-Activated Toxicity Against Microbial Infection 标题:Compounds With Copper-Or Zinc-Activated Toxicity Against Microbial Infection 摘要:具有新型吡唑硫酰胺基nnsn结构基元的杂环化合物,对微生物感染具有高效的锌或铜活化毒性,在微摩尔或纳摩尔最小抑制浓度(mic)下,以及制备和使用这些化合物的方法.
专利号:US-6136984-A 优先权日:1996-04-22 标 题 :Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes 发明人:DOERWALD FLORENCIO ZARAGOZA 权利人:NOVO NORDISK AS 摘要:A solid phase method for the synthesis of a plurality of differently substituted thiophenes with a wide variety of side-chain substituents as compounds of potential therapeutic interest is disclosed. The thiophenes are prepared by acylation of a substrate-bound primary or secondary amine with cyanoacetic acid and reaction of the resulting cyanoacetamide with an isothiocyanate in the presence of a base. Alkylation with an appropriate alkyl halide, followed by Thorpe-Ziegier-cyclization yields differently substituted, support-bound 3-aminothiophenes. These may be screened on the substrate or cleaved from the substrate and then screened in solution. Alternatively, the resin-bound 3-amino thiophenes or the synthetic intermediates can be subjected to further synthetic transformations (N-acylation, reduction) on the support, which permits the preparation of further therapeutically interesting compounds. The efficient synthesis of a wide variety of thiophenes using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse thiophene-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.
专利号:WO-9700244-A1 优先权日:1995-06-19 标题 :Process for parallel synthesis of a non-peptide library 发明人:FRITZ JAMES E; KALDOR STEPHEN W 权利人:LILLY CO ELI; FRITZ JAMES E; KALDOR STEPHEN W 摘要:A process for the sequential preparation of a library of compounds having pharmaceutical usage. The process involves the sequential mixing of solution phase reagents, followed by scavenging of excess unreacted reagents with solid phase scavenging agents. The process is highly iterative and applicable for producing various ureas, thiureas, amides, carbonates and tertiary amines.
专利号:WO-9740034-A1 优先权日:1996-04-22 标题:Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes
专利号:EP-1021435-A1 优先权日:1996-04-22 标题:Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes
专利号:EP-1776367-A1 优先权日:2004-07-27 标题 :Synthesis of 6,7-dihydro-5h-imidazoý1,2-a¨imidazole-3-sulfonic acid amides
专利号:WO-2006014828-A1 优先权日:2004-07-27 标题 :Synthesis of 6,7-dihydro-5h-imidazo[1,2-a]imidazole-3-sulfonic acid amides