专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

1. 发明授权

US09062012B2 Process for manufacturing 4-substituted amino-benzoxazinones 有权
标题翻译：制备4-取代氨基 - 苯并恶嗪酮的方法
公开(公告)号：US09062012B2
公开(公告)日：2015-06-23
申请号：US14365774
申请日：2012-12-20
申请人： Bernd Wolf , Joachim Gebhardt , Uwe Josef Vogelbacher , Maximilian Dochnahl , Michael Rack , Michael Keil , Timo Frassetto , Volker Maywald
发明人： Bernd Wolf , Joachim Gebhardt , Uwe Josef Vogelbacher , Maximilian Dochnahl , Michael Rack , Michael Keil , Timo Frassetto , Volker Maywald
IPC分类号： C07D265/36 , C07D413/04
CPC分类号： C07D265/36 , C07D413/04
摘要： The present invention relates to a process for manufacturing 4-substituted amino-benzoxazinones of formula (I), by reacting a NH-benzoxazinone of formula (II) with a compound of formula (III); wherein the variables are defined according to the description.
摘要翻译：本发明涉及式（I）的4-取代氨基 - 苯并恶嗪酮的制备方法，其中式（II）的N-苯并恶嗪酮与式（III）的化合物反应; 其中根据描述定义变量。

2. 发明授权

US09365495B2 Process for manufacturing aryloxyacetamides 有权
标题翻译：制备芳氧基乙酰胺的方法
公开(公告)号：US09365495B2
公开(公告)日：2016-06-14
申请号：US14365822
申请日：2012-12-20
申请人： Maximilian Dochnahl , Michael Rack , Michael Keil , Bernd Wolf , Uwe Josef Vogelbacher , Joachim Gebhardt , Timo Frassetto , Volker Maywald
发明人： Maximilian Dochnahl , Michael Rack , Michael Keil , Bernd Wolf , Uwe Josef Vogelbacher , Joachim Gebhardt , Timo Frassetto , Volker Maywald
IPC分类号： C07C231/24 , C07D413/04 , C07C231/12 , C07C235/20 , C07D207/06 , C07D211/06 , C07D295/185 , C07C235/34 , C07D207/16 , C07D211/16
CPC分类号： C07C231/24 , C07C231/12 , C07C235/20 , C07C235/34 , C07D207/06 , C07D207/16 , C07D211/16 , C07D295/185 , C07D413/04
摘要： The present invention relates to a process for manufacturing aryloxyacetamides of formula (I), by reacting haloacetamides of formula (II) with a phenol of formula (III); wherein the variables are defined according to the description, and aryloxyacetamides of formula (I).
摘要翻译：本发明涉及通过使式（II）的卤代乙酰胺与式（III）的苯酚反应制备式（I）的芳氧基乙酰胺的方法; 其中所述变量根据描述定义，和式（I）的芳氧基乙酰胺。

3. 发明申请

US20140357861A1 PROCESS FOR MANUFACTURING BENZOXAZINONES 有权
标题翻译：制备苯并恶嗪酮的方法
公开(公告)号：US20140357861A1
公开(公告)日：2014-12-04
申请号：US14365829
申请日：2012-12-20
申请人： Maximilian Dochnahl , Michael Rack , Michael Keil , Bernd Wolf , Uwe Josef Vogelbacher , Joachim Gebhardt , Timo Frassetto , Volker Maywald
发明人： Maximilian Dochnahl , Michael Rack , Michael Keil , Bernd Wolf , Uwe Josef Vogelbacher , Joachim Gebhardt , Timo Frassetto , Volker Maywald
IPC分类号： C07D265/36 , C07C231/12
CPC分类号： C07D265/36 , C07C231/12 , C07D413/04
摘要： The present invention relates to a process for manufacturing a benzoxazinone of formula (I), by reacting a nitro compound of formula (II) with a reducing agent to obtain an amino compound of formula (III), and then reacting the amino compound of formula (III) with an acid; wherein the variables are defined according to the description, and benzoxazinone of formula (I).
摘要翻译：本发明涉及式（I）的苯并恶嗪酮的制备方法，通式（II）的硝基化合物与还原剂反应得到式（III）的氨基化合物，然后使式（III）与酸反应; 其中根据描述定义变量，和式（I）的苯并嗪酮。

4. 发明授权

US09359312B2 Process for manufacturing benzoxazinones 有权
标题翻译：制备苯并恶嗪酮的方法
公开(公告)号：US09359312B2
公开(公告)日：2016-06-07
申请号：US14365829
申请日：2012-12-20
申请人： Maximilian Dochnahl , Michael Rack , Michael Keil , Bernd Wolf , Uwe Josef Vogelbacher , Joachim Gebhardt , Timo Frassetto , Volker Maywald
发明人： Maximilian Dochnahl , Michael Rack , Michael Keil , Bernd Wolf , Uwe Josef Vogelbacher , Joachim Gebhardt , Timo Frassetto , Volker Maywald
IPC分类号： C07D265/36 , C07D413/04 , C07C231/12
CPC分类号： C07D265/36 , C07C231/12 , C07D413/04
摘要： The present invention relates to a process for manufacturing a benzoxazinone of formula (I), by reacting a nitro compound of formula (II) with a reducing agent to obtain an amino compound of formula (III), and then reacting the amino compound of formula (III) with an acid; wherein the variables are defined according to the description, and benzoxazinone of formula (I).
摘要翻译：本发明涉及式（I）的苯并恶嗪酮的制备方法，通式（II）的硝基化合物与还原剂反应得到式（III）的氨基化合物，然后使式（III）与酸反应; 其中根据描述定义变量，和式（I）的苯并嗪酮。

5. 发明授权

US09000152B2 Process for manufacturing triazinon-benzoxazinones 有权
标题翻译：制备三嗪酮 - 苯并恶嗪酮的方法
公开(公告)号：US09000152B2
公开(公告)日：2015-04-07
申请号：US14364160
申请日：2012-12-20
申请人： Bernd Wolf , Volker Maywald , Uwe Josef Vogelbacher , Michael Rack , Maximilian Dochnahl , Michael Keil , Timo Frassetto , Joachim Gebhardt
发明人： Bernd Wolf , Volker Maywald , Uwe Josef Vogelbacher , Michael Rack , Maximilian Dochnahl , Michael Keil , Timo Frassetto , Joachim Gebhardt
IPC分类号： C07D413/14 , A01N43/84 , C07D413/04
CPC分类号： C07D413/04 , A01N43/84
摘要： The present invention relates to a process for manufacturing triazinon-benzoxazinones of formula (I), by reacting amino-benzoxazinones of formula (II) with 1,1′-carbonyldiimidazole (CDI) and a (thio)urea compound of formula (III); wherein the variables are defined according to the description.
摘要翻译：本发明涉及通过使式（II）的氨基 - 苯并嗪酮与1,1'-羰基二咪唑（CDI）和式（III）的（硫代）脲化合物反应制备式（I）的三嗪酮 - 苯并恶嗪酮的方法， ; 其中根据描述定义变量。

6. 发明申请

US20110144336A1 Method for Preparation of Piperazindione Derivatives 审中-公开
标题翻译：哌嗪二酮衍生物的制备方法
公开(公告)号：US20110144336A1
公开(公告)日：2011-06-16
申请号：US13058677
申请日：2009-07-30
申请人： Thomas Zierke , Eike Hupe , Michael Rack , Liliana Parra Rapado , Timo Frassetto
发明人： Thomas Zierke , Eike Hupe , Michael Rack , Liliana Parra Rapado , Timo Frassetto
IPC分类号： C07D241/08
CPC分类号： C07D241/08
摘要： A process for preparing piperazinedione derivatives of the formula I in which R1 is hydrogen, alkyl, alkenyl, alkynyl and alkylcarbonyl, R2 is hydrogen, alkyl, alkenyl, C3-C4-alkynyl and C(═O)R11, R3, R4 are each hydrogen, alkyl and haloalkyl, where the groups may be substituted, which comprises reacting amines of the formula II H2N—R1 II in which R1 is hydrogen and alkyl which may optionally be substituted with N-acylated amino acid derivatives of the formula III in which X is halogen, Y is halogen, alkoxy or phenyloxy which may be substituted and R2, R3 and R4 are each as defined at the outset, under basic conditions in an aqueous solvent.
摘要翻译：其中R 1是氢，烷基，烯基，炔基和烷基羰基，R 2是氢，烷基，烯基，C 3 -C 4炔基和C（= O）R 11，R 3，R 4各自是式I的哌嗪二酮衍生物的方法氢，烷基和卤代烷基，其中基团可以被取代，其包括使式II的其中R 1是氢的式IIH 2 N-R 1 II的烷基和可以被式III的N-酰化的氨基酸衍生物任选取代的烷基，其中 X是卤素，Y是可以被取代的卤素，烷氧基或苯氧基，R2，R3和R4各自在碱性条件下在水性溶剂中首先定义。

7. 发明申请

US20110207609A1 Piperazine Compounds With Herbicidal Effect 审中-公开
标题翻译：哌嗪化合物具有除草效果
公开(公告)号：US20110207609A1
公开(公告)日：2011-08-25
申请号：US13126658
申请日：2009-10-26
申请人： Liliana Parra Rapado , Frank Stelzer , Matthias Witschel , Thomas Seitz , Trevor William Newton , Julia Major , Tao Qu , William Karl Moberg , Dschun Song , Michael Rack , Timo Frassetto , Anja Simon , Robert Reinhard , Bernd Sievernich , Klaus Grossmann , Thomas Ehrhardt , Klaus Kreuz
发明人： Liliana Parra Rapado , Frank Stelzer , Matthias Witschel , Thomas Seitz , Trevor William Newton , Julia Major , Tao Qu , William Karl Moberg , Dschun Song , Michael Rack , Timo Frassetto , Anja Simon , Robert Reinhard , Bernd Sievernich , Klaus Grossmann , Thomas Ehrhardt , Klaus Kreuz
IPC分类号： A01N43/60 , C07D409/06 , C07D413/14 , A01N43/84 , C07D403/06 , C07D413/06 , A01N43/80 , A01P13/00
CPC分类号： C07D241/08
摘要： Piperazine compounds of the formula I in which the variables are defined according to the description, their agriculturally suitable salts, processes and intermediates for preparing the piperazines of the formula I, compositions comprising them and their use as herbicides, i.e. for controlling harmful plants, and also a method for controlling unwanted vegetation which comprises allowing a herbicidally effective amount of at least one piperazine compound of the formula I to act on plants, their seed and/or their habitat.
摘要翻译：式I的哌嗪化合物，其中根据描述定义变量，其农业上合适的盐，用于制备式I的哌嗪的方法和中间体，包含它们的组合物及其作为除草剂的用途，即用于防治有害植物，以及还包括控制不需要的植物的方法，其包括允许除草有效量的式I的至少一种哌嗪化合物作用于植物，其种子和/或其栖息地。

8. 发明申请

US20110183848A1 Piperazine Compounds With Herbicidal Effect 审中-公开
标题翻译：哌嗪化合物具有除草效果
公开(公告)号：US20110183848A1
公开(公告)日：2011-07-28
申请号：US13121976
申请日：2009-09-29
申请人： Liliana Parra Rapado , Frank Stelzer , Matthias Witschel , Thomas Seitz , Anja Simon , Robert Reinhard , Bernd Sievernich , Klaus Grossmann , Thomas Ehrhardt , Trevor Wlliam Newton , Julia Major , Tao Qu , William Karl Moberg , Dschun Song , Michael Rack , Timo Frassetto , Klaus Kreuz
发明人： Liliana Parra Rapado , Frank Stelzer , Matthias Witschel , Thomas Seitz , Anja Simon , Robert Reinhard , Bernd Sievernich , Klaus Grossmann , Thomas Ehrhardt , Trevor Wlliam Newton , Julia Major , Tao Qu , William Karl Moberg , Dschun Song , Michael Rack , Timo Frassetto , Klaus Kreuz
IPC分类号： A01N43/70 , C07D241/08 , A01N43/60 , A01P13/00 , C07D401/06 , A01N55/10 , C07F7/08
CPC分类号： C07D401/06 , C07D403/06
摘要： Piperazine compounds of the formula I in which the variables are defined according to the description, their agriculturally suitable salts, processes and intermediates for preparing the piperazine compounds of the formula I, compositions comprising them and their use as herbicides, i.e. for controlling harmful plants, and also a method for controlling unwanted vegetation which comprises allowing a herbicidally effective amount of at least one piperazine compound of the formula I to act on plants, their seed and/or their habitat.
摘要翻译：根据描述定义变量的哌嗪化合物，其农业上合适的盐，用于制备式I的哌嗪化合物的方法和中间体，包含它们的组合物及其作为除草剂的用途，即用于防治有害植物，以及用于控制不想要的植物的方法，其包括允许除草有效量的至少一种式I的哌嗪化合物作用于植物，其种子和/或其栖息地。

9. 发明申请

US20110130286A1 Piperazine Compounds with Herbicidal Effect 审中-公开
标题翻译：具有除草效果的哌嗪化合物
公开(公告)号：US20110130286A1
公开(公告)日：2011-06-02
申请号：US13056320
申请日：2009-07-23
申请人： Liliana Parra Rapado , Eike Hupe , Matthias Witschel , Thomas Seitz , Anja Simon , Robert Reinhard , Bernd Sievernich , Klaus Grossmann , Thomas Ehrhardt , Trevor William Newton , Frank Stelzer , Tao Qu , William Karl Moberg , Dschun Song , Michael Rack , Timo Frassetto , Klaus Kreuz , Julia Major
发明人： Liliana Parra Rapado , Eike Hupe , Matthias Witschel , Thomas Seitz , Anja Simon , Robert Reinhard , Bernd Sievernich , Klaus Grossmann , Thomas Ehrhardt , Trevor William Newton , Frank Stelzer , Tao Qu , William Karl Moberg , Dschun Song , Michael Rack , Timo Frassetto , Klaus Kreuz , Julia Major
IPC分类号： A01N57/16 , C07D401/06 , A01N43/60 , A01P13/00 , C07D401/14 , A01N43/84 , C07D413/14 , C07D491/08 , C07F9/145
CPC分类号： C07D401/06 , A01N43/60 , A01N43/78 , A01N43/80 , A01N43/82 , A01N43/84 , A01N43/90 , C07D403/06 , A01N33/18 , A01N43/54 , A01N2300/00
摘要： Piperazine compounds of the formula I in which the variables are defined according to the description, their agriculturally suitable salts, processes and intermediates for preparing the piperazine compounds of the formula I, compositions comprising them and their use as herbicides, i.e. for controlling harmful plants, and also a method for controlling unwanted vegetation which comprises allowing a herbicidally effective amount of at least one piperazine compound of the formula I to act on plants, their seed and/or their habitat.
摘要翻译：根据描述定义变量的哌嗪化合物，其农业上合适的盐，用于制备式I的哌嗪化合物的方法和中间体，包含它们的组合物及其作为除草剂的用途，即用于防治有害植物，以及用于控制不想要的植物的方法，其包括允许除草有效量的至少一种式I的哌嗪化合物作用于植物，其种子和/或其栖息地。

10. 发明授权

US08921567B2 Process for preparing N-substituted 1H-pyrazole-5-carbonylchloride compounds 有权
标题翻译：制备N-取代的1H-吡唑-5-碳酰氯化合物的方法
公开(公告)号：US08921567B2
公开(公告)日：2014-12-30
申请号：US14235556
申请日：2012-08-10
申请人： Karsten Körber , Prashant Deshmukh , Florian Kaiser , Michael Rack , Timo Frassetto , Gemma Veitch , Markus Kordes
发明人： Karsten Körber , Prashant Deshmukh , Florian Kaiser , Michael Rack , Timo Frassetto , Gemma Veitch , Markus Kordes
IPC分类号： C07D401/04
CPC分类号： C07D401/04
摘要： The present invention relates to a process for preparing an N-substituted 1H-pyrazole-5-carbonylchloride compound of the formula (I) in which R1 is hydrogen, halogen, cyano, C1-C6-alkyl, C1-C6-fluoroalkyl, C3-C8-cycloalkyl, C3-C8-fluorocycloalkyl, C2-C6-alkenyl, C2-C6-fluoroalkenyl, C1-C6-alkoxy, C1-C6-fluoroalkoxy, C1-C4-fluoroalkoxy-C1-C4-alkyl, phenyl and the like; each R2 is independently selected from halogen, C1-C6-alkyl, C1-C6-fluoroalkyl, C3-C8-cycloalkyl, C3-C8-fluorocycloalkyl, C2-C6-alkenyl, C2-C6-fluoroalkenyl, C1-C6-alkoxy, phenyl and the like; r is 0, 1, 2, 3 or 4; comprising the steps of i) deprotonating a compound of the formula (II) in which the variables R1, R2 and r are each as defined above, with a base selected from lithium-organic base having a carbon or nitrogen bound lithium or with a magnesium-organic base having a carbon bound magnesium; and ii) subjecting the product obtained in step (i) to a chlorocarbonylation by reacting it with a reagent selected from the group consisting of phosgene or a phosgene equivalent, to obtain a compound of formula (I).
摘要翻译：本发明涉及制备式（I）的N-取代的1H-吡唑-5-碳酰氯化合物的方法，其中R1是氢，卤素，氰基，C1-C6-烷基，C1-C6-氟烷基，C3 C 1-8 - 环烷基，C 3 -C 8 - 氟代环烷基，C 2 -C 6 - 烯基，C 2 -C 6 - 氟烯基，C 1 -C 6 - 烷氧基，C 1 -C 6 - 氟烷氧基，C 1 -C 4 - 氟烷氧基-C 1 -C 4烷基，苯基和喜欢; 每个R 2独立地选自卤素，C 1 -C 6 - 烷基，C 1 -C 6 - 氟代烷基，C 3 -C 8 - 环烷基，C 3 -C 8 - 氟代环烷基，C 2 -C 6 - 烯基，C 2 -C 6 - 氟烯基，C 1 -C 6烷氧基，苯基等; r为0,1,2,3或4; 包括以下步骤：i）将其中变量R1，R2和r各自如上定义的式（II）化合物与选自具有碳或氮键合的锂的锂基或与镁结合的碱的碱具有碳结合镁的无机碱; 和ii）通过使步骤（i）中获得的产物与选自光气或光气当量的试剂反应来进行氯羰化反应，得到式（I）化合物。

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