专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

81. 发明授权

US2393000A Process of preparing alkoxy propionyl compounds 失效
标题翻译：制备烷氧基丙酰化合物的方法
公开(公告)号：US2393000A
公开(公告)日：1946-01-15
申请号：US49607943
申请日：1943-07-24
申请人： WINGFOOT CORP
发明人： SEEGER NELSON V
CPC分类号： C07C255/13

82. 发明申请

US20170313647A1 Etheramine Compounds 审中-公开
公开(公告)号：US20170313647A1
公开(公告)日：2017-11-02
申请号：US15523418
申请日：2015-12-01
申请人： Huntsman Petrochemical LLC
发明人： Donald H Champion
IPC分类号： C07C217/08 , C07C213/02 , C07C255/13 , C07C253/30 , C07C2601/14
CPC分类号： C07C217/08 , C07C213/02 , C07C253/30 , C07C255/13 , C07C2601/14
摘要： Embodiments described herein provide a compound that may be used in a variety of applications such as corrosion inhibition, additives for metalworking, mining reagents, epoxy curatives, emulsifiers, fuel or lubricant additives, surfactant manufacture, acid scavengers and asphalt additives. The compound has the following structure: where R1 is a methoxy group, R2, R3, R4 and R5 are independently a hydrogen atom or an alkyl group, and R6 is an aminomethyl group.

83. 发明授权

US08691970B2 Phosphoramidite compound and method for producing oligo-RNA 有权
标题翻译：亚磷酰胺化合物及其制备方法
公开(公告)号：US08691970B2
公开(公告)日：2014-04-08
申请号：US11574308
申请日：2005-08-25
申请人： Tadaaki Ohgi , Kouichi Ishiyama , Yutaka Masutomi
发明人： Tadaaki Ohgi , Kouichi Ishiyama , Yutaka Masutomi
IPC分类号： C07H19/04 , C07H21/02
CPC分类号： C07C255/13 , C07H19/067 , C07H19/167 , C07H21/02 , Y02P20/55 , Y02P20/582
摘要： An object of the present invention is to provide a useful and novel phosphoramidite compound for the synthesis of oligo-RNA.A phosphoramidite compound represented by general formula (1), wherein: BX represents a nucleobase optionally having a protecting group; and R1 is a substituent represented by general formula (2), wherein: R11, R12 and R13 are the same or different and each represents hydrogen or alkoxy; R2a and R2b are the same or different and each represents alkyl, or R2a and R2b taken together with the adjacent nitrogen atom may form a 5- to 6-membered saturated amino cyclic group, the amino cyclic group optionally having an oxygen or sulfur atom as a ring-composing member in addition to the adjacent nitrogen atom; and WG1 and WG2 are the same or different and each represents an electron-withdrawing group.
摘要翻译：本发明的目的是提供一种用于合成寡聚RNA的有用和新型的亚磷酰胺化合物。由通式（1）表示的亚磷酰胺化合物，其中：BX表示任选具有保护基的核碱基; 并且R 1是由通式（2）表示的取代基，其中：R 11，R 12和R 13相同或不同，各自表示氢或烷氧基; R2a和R2b相同或不同，各自表示烷基，或者R2a和R2b与相邻氮原子一起可以形成5-至6-元饱和的氨基环状基团，氨基环状基团任选具有氧或硫原子作为除了相邻的氮原子之外的环组成成分; WG1和WG2相同或不同，各自表示吸电子基团。

84. 发明申请

US20140018567A1 METHOD FOR PREPARING DINITRILE COMPOUND 有权
标题翻译：制备DINITRILE化合物的方法
公开(公告)号：US20140018567A1
公开(公告)日：2014-01-16
申请号：US14026233
申请日：2013-09-13
申请人： LG CHEM, LTD.
发明人： Byoung-Bae LEE , Jae-Seung OH , You-Jin SHIM , Yeon-Suk HONG
IPC分类号： C07C253/30
CPC分类号： C07C253/30 , B01J31/0212 , B01J2231/32 , C07C255/13
摘要： Disclosed is a method for preparing a dinitrile compound. The method includes reacting an alcohol compound with a nitrile compound having a terminal carbon-carbon unsaturated bond under anhydrous conditions. A potassium alkoxide having 1 to 5 carbon atoms is used as a catalyst in the course of the reaction. According to the method, a high-purity dinitrile compound can be prepared in a simple manner within a short reaction time indicating high productivity.
摘要翻译：公开了二腈化合物的制备方法。该方法包括在无水条件下使醇化合物与具有末端碳 - 碳不饱和键的腈化合物反应。在反应过程中使用具有1至5个碳原子的醇盐作为催化剂。根据该方法，可以在短的反应时间内以简单的方式制备高纯度二腈化合物，表明生产率高。

85. 发明申请

US20130317245A1 INTERMEDIATES FOR THE SYNTHESIS OF BENZINDENE PROSTAGLANDINS AND PREPARATIONS THEREOF 有权
公开(公告)号：US20130317245A1
公开(公告)日：2013-11-28
申请号：US13954191
申请日：2013-07-30
申请人： Shih-Yi WEI , Min-Kuan HSU , Ming-Kun HSU
发明人： Shih-Yi WEI , Min-Kuan HSU , Ming-Kun HSU
IPC分类号： C07F7/08 , C07C255/13 , C07C69/017 , C07C37/055
CPC分类号： C07F7/081 , C07C37/003 , C07C37/0555 , C07C37/50 , C07C41/26 , C07C51/08 , C07C51/09 , C07C67/283 , C07C67/297 , C07C69/017 , C07C69/18 , C07C69/78 , C07C255/13 , C07C2603/14 , C07F7/1804 , Y02P20/55 , C07C39/23 , C07C39/17 , C07C43/23 , C07C69/732 , C07C59/72
摘要： Novel processes for preparing optically active cyclopentanones 1 which are useful for the preparation of benzindene Prostaglandins and novel cyclopentanones are provided. The invention also provides novel processes of preparing benzindene Prostaglandins and novel intermediates for benzindene Prostaglandins.

86. 发明授权

US08569535B2 Substituted benzoylamino-indan-2-carboxylic acids and related compounds 有权
标题翻译：取代的苯甲酰氨基 - 茚满-2-羧酸及相关化合物
公开(公告)号：US08569535B2
公开(公告)日：2013-10-29
申请号：US12627546
申请日：2009-11-30
申请人： Thomas Joseph Caulfield , Jennifer Williford Clemens , Robert S. Francis , Brian Scott Freed , Stanly John , Tieu-Binh Le , Brian Pedgrift , Antonio Daniel Ramos , Gerard Charles Rosse , Martin Smrcina , David Squire Thorpe , William Shelly Wire , Jianhong Zhao
发明人： Thomas Joseph Caulfield , Jennifer Williford Clemens , Robert S. Francis , Brian Scott Freed , Stanly John , Tieu-Binh Le , Brian Pedgrift , Antonio Daniel Ramos , Gerard Charles Rosse , Martin Smrcina , David Squire Thorpe , William Shelly Wire , Jianhong Zhao
IPC分类号： C07C229/00
CPC分类号： C07D333/78 , C07C233/52 , C07C233/63 , C07C233/81 , C07C235/42 , C07C235/54 , C07C235/62 , C07C235/84 , C07C237/42 , C07C255/13 , C07C255/57 , C07C311/09 , C07C311/29 , C07C317/44 , C07C323/62 , C07C2601/02 , C07C2601/04 , C07C2601/08 , C07C2601/10 , C07C2602/08 , C07C2602/10 , C07C2602/42 , C07C2603/26 , C07C2603/28 , C07C2603/74 , C07D213/81 , C07D307/79 , C07D333/68 , C07D401/04
摘要： The present invention relates to novel compounds of the formula Ia: in any of its stereoisomeric forms or a mixture of stereoisomeric forms in any ratio, or a physiologically acceptable salt thereof, wherein the substituents are as described herein. The inventive compounds have CXCR5 inhibitory activity, and are particularly useful in treating or preventing various inflammatory diseases, such as rheumatoid arthritis, multiple sclerosis, lupus, Crohn's Disease, associated with the modulation of the human CXCR5 receptor.
摘要翻译：本发明涉及式Ia的新化合物：其任何立体异构体形式或任何比例的立体异构形式的混合物或其生理上可接受的盐，其中取代基如本文所述。本发明化合物具有CXCR5抑制活性，并且特别可用于治疗或预防与人CXCR5受体的调节相关的各种炎性疾病，例如类风湿性关节炎，多发性硬化，狼疮，克罗恩病。

87. 发明申请

US20130231494A1 METHOD OF MAKING FLUORINATED ALKOXY CARBOXYLIC ACIDS AND PRECURSORS THEREOF 有权
标题翻译：制备氟化烷氧基羧酸及其前体的方法
公开(公告)号：US20130231494A1
公开(公告)日：2013-09-05
申请号：US13862905
申请日：2013-04-15
申请人： 3M INNOVATIVE PROPERTIES COMPANY
发明人： Tilman C. Zipplies , Klaus Hintzer , Oleg Shyshkov
IPC分类号： C07C255/13 , C07C253/14 , C07C51/08 , C07C247/04
CPC分类号： C07C255/13 , C07C51/08 , C07C59/135 , C07C67/08 , C07C69/708 , C07C247/04 , C07C253/14
摘要： Provided are saturated partially fluorinated alkoxy carboxylic acids or salts thereof and methods of preparation.
摘要翻译：提供的是饱和部分氟化的烷氧基羧酸或其盐及其制备方法。

88. 发明申请

US20130053581A1 INTERMEDIATES FOR THE SYNTHESIS OF BENZINDENE PROSTAGLANDINS AND PREPARATIONS THEREOF 有权
标题翻译：合成苯并芘前体的中间体及其制备方法
公开(公告)号：US20130053581A1
公开(公告)日：2013-02-28
申请号：US13216378
申请日：2011-08-24
申请人： Shih-Yi WEI , Min-Kuan Hsu , Ming-Kun Hsu
发明人： Shih-Yi WEI , Min-Kuan Hsu , Ming-Kun Hsu
IPC分类号： C07C51/09 , C07C51/08 , C07C69/78 , C07C255/16 , C07C69/017 , C07F7/18 , C07C37/00
CPC分类号： C07F7/081 , C07C37/003 , C07C37/0555 , C07C37/50 , C07C41/26 , C07C51/08 , C07C51/09 , C07C67/283 , C07C67/297 , C07C69/017 , C07C69/18 , C07C69/78 , C07C255/13 , C07C2603/14 , C07F7/1804 , Y02P20/55 , C07C39/23 , C07C39/17 , C07C43/23 , C07C69/732 , C07C59/72
摘要： Novel processes for preparing optically active cyclopentanones 1 which are useful for the preparation of benzindene Prostaglandins and novel cyclopentanones are provided. The invention also provides novel processes of preparing benzindene Prostaglandins and novel intermediates for benzindene Prostaglandins.
摘要翻译：提供了可用于制备苯撑前列腺素和新型环戊烷酮的光学活性环戊酮1的新方法。本发明还提供了制备苯并茚前列腺素的新方法和苯并ene前列腺素的新中间体。

89. 发明申请

US20110319641A1 TREPROSTINIL PRODUCTION 有权
标题翻译：曲妥珠单抗生产
公开(公告)号：US20110319641A1
公开(公告)日：2011-12-29
申请号：US13151465
申请日：2011-06-02
申请人： Hitesh Batra , Raju Penmasta , Vijay Sharma , Sudersan M. Tuladhar , David A. Walsh
发明人： Hitesh Batra , Raju Penmasta , Vijay Sharma , Sudersan M. Tuladhar , David A. Walsh
IPC分类号： C07D309/12 , C07C51/08 , C07C41/08 , C07C67/347 , C07C253/30 , C07F7/18 , C07C51/09
CPC分类号： C07C51/00 , C07B2200/07 , C07C29/143 , C07C29/42 , C07C45/00 , C07C45/29 , C07C45/61 , C07C45/64 , C07C51/09 , C07C51/367 , C07C59/72 , C07C67/343 , C07C253/30 , C07F7/1892 , Y02P20/55 , C07C69/736 , C07C255/13
摘要： The present invention is directed to a novel method for preparing a synthetic intermediate for treprostinil via a stereoselective alkyne addition reaction. Also described are methods of preparing treprostinil comprising the alkyne addition reaction described herein as well as novel intermediates useful for synthesis prostacyclin derivatives, such as treprostinil.
摘要翻译：本发明涉及通过立体选择性炔炔加成反应制备曲前列素的合成中间体的新方法。还描述了制备包含本文所述的炔炔加成反应的曲前列素的方法以及可用于合成前列环素衍生物例如曲前列素的新型中间体。

90. 发明申请

US20110168636A1 CHELATING COMPOUNDS AND IMMOBILIZED TETHERED CHELATORS 有权
标题翻译：化学化合物和固定化的螯合剂
公开(公告)号：US20110168636A1
公开(公告)日：2011-07-14
申请号：US13052477
申请日：2011-03-21
申请人： Robert A. Yokel , Wesley R. Harris , Christopher D. Spilling , Chang-Guo Zhan
发明人： Robert A. Yokel , Wesley R. Harris , Christopher D. Spilling , Chang-Guo Zhan
IPC分类号： B01D15/38
CPC分类号： C07C259/06 , B01D15/3828 , B01J20/3204 , B01J20/321 , B01J20/3212 , B01J20/3219 , B01J20/3251 , B01J20/3253 , C02F2101/20 , C07C217/28 , C07C255/13 , C07C311/17 , C08F8/28 , C08F8/30 , C08F12/30 , C08F212/08 , C08F212/36 , C08F212/14 , C08F8/36
摘要： Methods are described for removing aluminum from a solution using novel di- and tripodal compounds as chelators.
摘要翻译：描述了使用新的二 - 和三峰化合物作为螯合剂从溶液中除去铝的方法。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式