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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。
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公开(公告)号:US20120220781A1
公开(公告)日:2012-08-30
申请号:US13505909
申请日:2010-10-28
申请人: Maximilian Dochnahl , Michael Keil , Bernd Wolf
发明人: Maximilian Dochnahl , Michael Keil , Bernd Wolf
IPC分类号: C07D409/12 , C07D231/14
CPC分类号: C07D231/14
摘要: A process for preparing 1,3-disubstituted pyrazole compounds.
摘要翻译: 制备1,3-二取代吡唑化合物的方法。
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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。
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公开(公告)号:US20140206884A1
公开(公告)日:2014-07-24
申请号:US14223103
申请日:2014-03-24
申请人: Maximilian DOCHNAHL , Michael KEIL , Joachim GEBHARDT , Uwe Josef VOGELBACHER , Frederik MENGES , Michael RACK , Jens RENNER , Bernd WOLF
发明人: Maximilian DOCHNAHL , Michael KEIL , Joachim GEBHARDT , Uwe Josef VOGELBACHER , Frederik MENGES , Michael RACK , Jens RENNER , Bernd WOLF
IPC分类号: A01N43/653 , A01N55/00
CPC分类号: A01N43/653 , A01N55/00 , C07D249/08 , C07D403/04 , C07D405/06 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D487/08 , C07F3/003 , C07F3/02
摘要: The present invention relates to a process using Grignard reagents for providing thio-triazolo group-containing compounds.
摘要翻译: 本发明涉及使用格氏试剂提供含硫代三唑基的化合物的方法。
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公开(公告)号:US08729272B2
公开(公告)日:2014-05-20
申请号:US13583798
申请日:2011-03-15
申请人: Maximilian Dochnahl , Michael Keil , Joachim Gebhardt , Uwe Josef Vogelbacher , Frederik Menges , Michael Rack , Jens Renner , Bernd Wolf
发明人: Maximilian Dochnahl , Michael Keil , Joachim Gebhardt , Uwe Josef Vogelbacher , Frederik Menges , Michael Rack , Jens Renner , Bernd Wolf
IPC分类号: C07D405/06 , C07D249/08
CPC分类号: A01N43/653 , A01N55/00 , C07D249/08 , C07D403/04 , C07D405/06 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D487/08 , C07F3/003 , C07F3/02
摘要: The present invention relates to a process using Grignard reagents for providing thio-triazolo group-containing compounds.
摘要翻译: 本发明涉及使用格氏试剂提供含硫代三唑基的化合物的方法。
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公开(公告)号:US08362272B2
公开(公告)日:2013-01-29
申请号:US13505909
申请日:2010-10-28
申请人: Maximilian Dochnahl , Michael Keil , Bernd Wolf
发明人: Maximilian Dochnahl , Michael Keil , Bernd Wolf
IPC分类号: C07D231/10
CPC分类号: C07D231/14
摘要: A process for preparing 1,3-disubstituted pyrazole compounds.
摘要翻译: 制备1,3-二取代吡唑化合物的方法。
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公开(公告)号:US20130005985A1
公开(公告)日:2013-01-03
申请号:US13583798
申请日:2011-03-15
申请人: Maximilian Dochnahl , Michael Keil , Joachim Gebhardt , Uwe Josef Vogelbacher , Frederik Menges , Michael Rack , Jens Renner , Bernd Wolf
发明人: Maximilian Dochnahl , Michael Keil , Joachim Gebhardt , Uwe Josef Vogelbacher , Frederik Menges , Michael Rack , Jens Renner , Bernd Wolf
IPC分类号: C07D249/12 , C07D403/02 , C07D409/06
CPC分类号: A01N43/653 , A01N55/00 , C07D249/08 , C07D403/04 , C07D405/06 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D487/08 , C07F3/003 , C07F3/02
摘要: The present invention relates to a process using Grignard reagents for providing thio-triazolo group-containing compounds.
摘要翻译: 本发明涉及使用格氏试剂提供含硫代三唑基的化合物的方法。
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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。
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公开(公告)号:US20130184465A1
公开(公告)日:2013-07-18
申请号:US13876326
申请日:2011-09-27
IPC分类号: C07D405/02
CPC分类号: C07D405/02 , C07D249/10 , C07D405/06 , C07F3/02 , Y02P20/582
摘要: The present invention relates to a process using specific magnesium reagents for providing thio-triazolo group-containing compounds and for the synthesis of precursors therefor. The invention furthermore relates to intermediates and to their preparation.
摘要翻译: 本发明涉及使用特定的镁试剂来提供含硫代三唑基的化合物和用于合成其前体的方法。 本发明还涉及中间体及其制备方法。
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公开(公告)号:US08362271B2
公开(公告)日:2013-01-29
申请号:US13393624
申请日:2010-09-03
IPC分类号: C07D231/10
CPC分类号: C07D231/20 , C07D231/14
摘要: The present invention to a process for preparing 1-phenylpyrazoles of the formula I in which each R1 is independently selected from chlorine, fluorine, alkyl, haloalkyl, alkoxy and haloalkoxy; n is 1, 2 or 3; each R2 is independently selected from cyano, nitro, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio and alkoxycarbonyl; m is 0, 1 or 2; A is alkyl, aryl or aryl-C1-C4-alkyl, where A optionally bears 1, 2, 3 or 4 substituents comprising reacting a phenyl halide of the formula (II) with apyrazole derivative of the formula (III) in which X is chlorine, iodine or bromine; and R1, n, R2, m and A are each as defined above, in the presence of a base and a catalytic system comprising a ligand and a metal compound selected from palladium compounds, iron compounds and copper compounds.
摘要翻译: 本发明涉及一种制备式I的1-苯基吡唑的方法,其中每个R 1独立地选自氯,氟,烷基,卤代烷基,烷氧基和卤代烷氧基; n为1,2或3; 每个R 2独立地选自氰基,硝基,卤素,烷基,卤代烷基,烷氧基,卤代烷氧基,烷硫基和烷氧基羰基; m为0,1或2; A是烷基,芳基或芳基-C 1 -C 4 - 烷基,其中A任选地带有1,2,3或4个取代基,包括使式(II)的苯基卤与式(III)的吡咯衍生物反应,其中X为 氯,碘或溴; 在碱和催化体系的存在下,R 1,n,R 2,m和A各自如上所定义,所述催化体系包含配体和选自钯化合物,铁化合物和铜化合物的金属化合物。
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