CAS: 26944-71-8; 2-Bromo-6-Hydrazinylpyridine

该化合物是一种有机化合物,其特点是以溴原子和氢氨功能组组成的环取代了环,其分子结构中含有氮的芳香环有六人,有助于其反应和各种化学反应的潜在应用;溴原子的存在增强了其电子生殖特性,使其在核生殖替代反应中有用;氢氨组引入了进一步衍生的可能性,允许合成更复杂的分子;该化合物通常用于医药化学和研究,特别是用于制药和农用化学研究;它可能展示生物活动,可以用于治疗用途;与许多含氮化合物一样,必须处理2-Bromo-6-hydizonopyprididine,并注意潜在的毒性和再活性.在实验室环境中与该物质合作时,应当遵循适当的安全议定书.

结构式图片

相似化合物

19798-81-3 1019918-39-8 77992-44-0

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CAS号626-05-1 2,6-二溴吡啶 | CAS号144100-07-2 2-溴-6-氟吡啶 | CAS号1128268-00-7 1H-pyrazole-4-c... | CAS号864933-07-3 5-溴-[1,2,4]噻唑并[...

合成工艺路线路线简述

  • 合成目标产物 2-Bromo-6-Hydrazinylpyridine 主要起始原料 2,6-Dibromopyridine
  • (文献来源)合成步骤主要原料 2,6-Dibromopyridine
2,6-二溴吡啶置于一水合肼体系中,用 正丁醇 用作溶剂,化学反应 5.0H,以63%的收率获得2-溴-6-肼基吡啶
参考文献:多功能高旋转双自由基吡唑基吡啶-双硝基硝基硝基氧化物.
标题:多功能高旋转双自由基吡唑基吡啶-双硝基硝基硝基氧化物.
摘要:[结构:见正文]描述了附着在吡唑基吡啶上的功能性硝酰基-和亚氨基硝基氧化物的合成,紫外-可见,红外和epr光谱表征以及x射线结构分析.发现亚硝酰氮氧化物之间的交换相互作用比亚氨基硝化物更强.尽管用吡唑环取代吡啶导致距离更短和偶极耦合更大,但交换相互作用却减少了.当化合物1固态形成二聚体时,三联吡啶3导致超分子π堆积.
Doi:10.1021/ol0479040

海关参考信息

专利信息


专利号:WO-2013057110-A1
优先权日:2011-10-19
标 题:Method for the synthesis of citric acid esters
发明人:ALTENBACH HANS-JOSEF; LANGE KARSTEN; NANDI SUKHENDU; IHIZANE RACHID; JAKOB BERND; SCHNEIDER MANFRED
权利人:BERGISCHE UNI WUPPERTAL; ALTENBACH HANS-JOSEF; LANGE KARSTEN; NANDI SUKHENDU; IHIZANE RACHID; JAKOB BERND; SCHNEIDER MANFRED
摘要:The present invention discloses a targeted synthesis method for the synthesis of asymmetric monoesters and/or symmetrical diesters of citric acid through acidic esterification by using boric acid or a boronic acid as a catalyst. The boric/boronic acid simultaneously acts as a catalyst, as well as a 'protecting group' for the tertiary carboxylic acid, and therefore specifically only the asymmetric monoesters or symmetrical diesters are created.

专利号:WO-9507882-A1
优先权日:1993-09-14
标 题:Synthesis of amido acids from carboxylic acid esters and amino acid salts
发明人:HEINZMAN STEPHEN WAYNE; DUPONT JEFFREY SCOTT
权利人:PROCTER & GAMBLE
摘要:Chemical synthesis of amido acids, and their conversion to amido acid phenyl ester sulfonates for use as bleach activators, starting from carboxylic acid esters and amino acid salts.

专利号:US-5534642-A
优先权日:1993-09-14
标题 :Synthesis of amido acids from carboxylic acids and lactams
发明人:HEINZMAN STEPHEN W; DUPONT JEFFREY S; TETTENHORST WILLIAM C
权利人:PROCTER & GAMBLE
摘要:Chemical synthesis of amido acids, and their conversion to amido acid phenyl ester sulfates for use as bleach activators, starting from carboxylic acids and lactams.

专利号:US-9765044-B2
优先权日:2013-03-15
标 题 :Synthesis of novel ionic liquids from lignin-derived compounds
发明人:SOCHA AARON; SINGH SEEMA; SIMMONS BLAKE A; BERGERON MAXIME
权利人:UNIV CALIFORNIA; SANDIA CORP
摘要:Methods and compositions are provided for synthesizing ionic liquids from lignin derived compounds comprising: contacting a starting material comprising lignin with a depolymerization agent to depolymerize the lignin and form a mixture of aldehyde containing compounds; contacting the mixture of aldehyde containing compounds with an amine under conditions suitable to convert the mixture of aldehyde containing compounds to a mixture of amine containing compounds; and contacting the mixture of amine containing compounds with an acid under conditions suitable to form an ammonium salt, thereby preparing the ionic liquid.

专利号:US-3589865-A
优先权日:1968-07-30
标题:Synthesis of ammonia
发明人:TAMELEN EUGENE E VAN
权利人:UNIV LELAND STANFORD JUNIOR
摘要:MOLECULAR NITROGEN IS CONVERTED TO AMMONIA AT ROOM TEMPERATURE AND ATMOSPHERE PRESSURE BY A PROCESS OF CONTACTING NITROGEN OR AIR WITH A TIIV OR TIIII COMPOUND DURING ITS REDUCTION TO A TIII COMPOUND IN A SUITABLE SOLVENT, FOLLOWED BY ADDITION OF A PROTONATING AGENT. THE PROCESS MAY BE USED FOR PURPOSES OTHER THAN THE PRODUCTION OF AMMONIA, SUCH AS SCAVENGING GASES OR SENSING THE PRESENCE OF NITROGEN OR OXYGEN.

专利号:US-9309215-B2
优先权日:2006-06-12
标题:Chiral intermediate, process for producing the same and its use in the manufacture of tolterodine, fesoterodine, or the active metabolite thereof
发明人:MEESE CLAUS
权利人:UCB PHARMA GMBH
摘要:The compound of formula (I): is provided. It may be produced by subjecting a compound of formula (IV) to a reduction reaction wherein R represents hydrogen, straight or branched C1-C6 alkyl. This compound is a valuable intermediate which may be used in the synthesis of fesoterodine, tolterodine, its active metabolite, and related compounds.
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合成参考文献


参考文献:10.1007/bf00475876
摘要:Yakhontov LN, Pronina EV. Fischer cyclization of 6-substituted pyrid-2-ylhydrazones of cyclohexanone. Chemistry of Heterocyclic Compounds. 1972 Nov;5(6):851–5. doi: 10.1007/bf00475876.
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