CAS: 17852-67-4; (4-(Methylsulfonyl)Phenyl)Hydrazine Hydrochloride

该化合物是一种化学化合物,其特征是附于一个苯环的氢子功能组,该化合物还被一个甲基硫磺基组所取代,该化合物一般是白色的脱白晶状固体,在水和各种有机溶剂中溶解,使其在不同化学应用中有用;它经常用于有机合成和制药研究,特别是在开发潜在治疗剂方面;甲基硫酰胺组的存在加强了其再活动,能够影响其生物活动;它与许多氢氨衍生物一样,它可能表现出抗氧化剂活动或潜在细胞毒性等特性,需要仔细处理和考虑安全议定书;此外,必须指出,此类化合物可能因其潜在的生物影响而具有具体的监管考虑;经常参考安全数据表和有关文献,以便详细处理和使用准则.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

4-methanesulfonylphenylamine 4-bromoohenyl methyl sulfone 5-(4-Fluoro-phenyl)-1-(4-methanesulfonyl-phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester 1-(4-methanesulfonylphenyl)-5-phenyl-1H-pyrazole-3-carboxylic acid ethyl ester H-pyrazole-4-carboxylic acid ethyl ester5-(4-fluoro-phenyl)-1-(4-methanesulfonyl-phenyl)-1H-pyrazole-4-carboxylic acid ethyl ester

合成工艺路线路线简述

  • 合成目标产物 4-(Methylsulfonyl)Phenylhydrazine Hydrochloride 主要起始原料 4-Methylsulfonylaniline
  • (文献来源)合成步骤主要原料 4-Methylsulfonylaniline
📜4-溴苯甲砜置于potassium Phosphate,Copper(L) Iodide,N,N'-二(2,6-二甲基苯基)草酰胺,十六烷基三甲基溴化铵,一水合肼,盐酸体系中,用 水 用作溶剂,化学反应 0.25H,以0.444 G的收率获得4-(甲基磺酰基)苯肼盐酸盐
参考文献:Cui / Bmpo催化卤代芳烃与水合肼的交叉偶联合成芳族肼
标题:Cui / Bmpo催化卤代芳烃与水合肼的交叉偶联合成芳族肼
摘要:的n,N-双(2,6-二甲基苯基)草酰胺,发现作为一个强大的配体对cu催化的与水合肼芳基卤化物的交叉耦合,从而导致的各种芳基肼的形成在80 ö用c在k 3 Po 4和4 Mol%的十六烷基三甲基溴化铵的帮助下,从芳基溴化物和芳基碘化物中加入水.在大多数情况下,观测到非常好至极好的产量.
Doi:10.1002/cjoc.201800326

海关参考信息

专利信息


专利号:US-7442802-B2
优先权日:2002-06-27
标 题:Cyclooxygenase-2 selective inhibitors, compositions and methods of use
发明人:BANDARAGE UPUL K; EARL RICHARD A; EZAWA MAIKO; FANG XINQIN; GARVEY DAVID S; KHANAPURE SUBHASH P; RANATUNGE RAMANI R; RICHARDSON STEWART K; SCHROEDER JOSEPH D; STEVENSON CHERI A; WEY SHIOW-JYI
权利人:NITROMED INC
摘要:The invention describes novel cyclooxygenase 2 (COX-2) selective inhibitors and novel compositions comprising at least one cyclooxygenase 2 (COX-2) selective inhibitor, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one COX-2 selective inhibitor, optionally nitrosated and/or nitrosylated, and, optionally, at least one nitric oxide donor, and/or, optionally, at least one therapeutic agent. The novel cyclooxygenase 2 selective inhibitors of the invention can be optionally nitrosated and/or nitrosylated. The invention also provides methods for treating inflammation, pain and fever; for treating and/or improving the gastrointestinal properties of COX-2 selective inhibitors; for facilitating wound healing; for treating and/or preventing renal and/or respiratory toxicity; for treating and/or preventing other disorders resulting from elevated levels of cyclooxygenase-2; and for improving the cardiovascular profile of COX-2 selective inhibitors.

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📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:Synthesis Of Indolo[2,1-A]Isoquinoline Derivatives Via Visible-Light-Induced Radical Cascade Cyclization Reactions
作者:Yun-Long Wei,Jian-Qiang Chen,Bo Sun,Peng-Fei Xu
摘要:We Describe A Photocatalyzed Transformation For The Synthesis Of The Indolo[2,1-A]Isoquinoline Core Structure. This Redox Neutral Reaction Features Mild Reaction Conditions And Exceptional Functional Group Tolerance. A Series Of Valuable Indolo[2,1-A]Isoquinoline Derivatives Bearing Various Functional Groups Were Synthesized Using This Method In Good To Excellent Yields.

合成参考文献


参考文献:10.1007/s11030-025-11220-8
摘要:Fadaly WAA, Elshewy A, Abusabaa AHA, Amin DME, Abdelhady HK, Haredy HH, Mahmoud AM, Ibrahim NA, Nemr MTM. Novel pyrazole carboxylate derivatives as lonazolac bioisosteres with selective COX-2 inhibition: design, synthesis and anti-inflammatory activity. Mol Divers. 2025 May 22;30(1):933–58. doi: 10.1007/s11030-025-11220-8.
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