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1.发明公开VERFAHREN ZUR HERSTELLUNG VON CIS-ALKOXYSUBSTITUIERTEN SPIROCYCLISCHEN PHENYLACETYLAMINOSÄUREESTERN UND CIS-ALKOXYSUBSTITUIERTEN SPIROCYCLISCHEN 1-H-PYRROLIDIN-2,4-DION-DERIVATEN 有权维生素ZER HERSTELLUNG VON CIS-ALKOXYSUBSTITUIERTEN螺环化合物苯丙氨酸氨基脲在CIS-ALKOXYSUBSTITUIERTEN SPIROCYCLISENEN 1-H-吡咯烷-2,4-二酮衍生物
公开(公告)号：EP2831038A1
公开(公告)日：2015-02-04
申请号：EP13712251.1
申请日：2013-03-25
IPC分类号： C07C231/12 , C07C233/52 , C07D263/52 , C07D209/96
CPC分类号： C07C233/51 , C07C231/12 , C07C233/52 , C07C2601/14 , C07D209/54 , C07D263/52
摘要： The present invention relates to a novel process for preparing cis-alkoxy-substituted spirocyclic phenylacetylamino acid esters and cis-alkoxy-substituted spirocyclic 1-H-pyrrolidine-2,4-dione derivatives and also novel intermediates and starting compounds which go through or are used in the process of the invention.
摘要翻译： 本发明涉及一种制备顺式 - 烷氧基取代的螺环苯乙酰氨基酸酯和顺式 - 烷氧基取代的螺环-1H-吡咯烷-2,4-二酮衍生物的新方法，还涉及生产和/ 或用于根据本发明的方法中。
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2.发明授权VERFAHREN ZUR HERSTELLUNG VON CIS-ALKOXYSUBSTITUIERTEN SPIROCYCLISCHEN PHENYLACETYLAMINOSÄUREESTERN UND CIS-ALKOXYSUBSTITUIERTEN SPIROCYCLISCHEN 1-H-PYRROLIDIN-2,4-DION-DERIVATEN 有权VERFAHREN ZUR HERSTELLUNG VON CIS-ALKOXYSUBSTITUIERTEN SPIROCYCLISCHEN苯基乙酰氨基己酸酯和CIS-ALKOXYSUBSTITUIERTEN SPIROCYCLISCHEN 1-H-吡咯烷-2,4-二酮 - 衍生物
公开(公告)号：EP2831038B1
公开(公告)日：2017-07-19
申请号：EP13712251.1
申请日：2013-03-25
发明人： FARIDA, Taraneh , MAIWALD, Berndt , LITTMANN, Martin , ETZEL, Winfried , WARSITZ, Rafael , HENCK, Nioclas , ESSER, Michael
IPC分类号： C07C231/12 , C07C233/52 , C07D263/52 , C07D209/96
CPC分类号： C07C233/51 , C07C231/12 , C07C233/52 , C07C2601/14 , C07D209/54 , C07D263/52
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公开(公告)号：EP2558473B1
公开(公告)日：2016-09-07
申请号：EP11712882.7
申请日：2011-04-08
发明人： HIMMLER, Thomas , ETZEL, Winfried , VOLZ, Frank
IPC分类号： C07D495/14 , C07D207/456
CPC分类号： C07D495/14 , C07D207/456
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4.发明公开METHOD FOR THE PREPARATION OF PERFLUOROALKYL CONTAINING PYRAZOLES CARBOXYLATES 有权用于生产全氟烷基PYRAZOLCARBOXYLATEN
公开(公告)号：EP2882717A1
公开(公告)日：2015-06-17
申请号：EP13745830.3
申请日：2013-08-02
申请人： Bayer CropScience AG
发明人： PAZENOK, Sergii , ETZEL, Winfried , LUI, Norbert , NEEFF, Arnd
IPC分类号： C07D231/16 , C07C17/00
CPC分类号： C07D231/16 , C07C17/00 , C07C67/343 , C07C69/716
摘要： The present invention pertains to a novel process for the preparation of Fluoroalkylpyrazole- or Bisperfluoroalkypyrazole carboxylates (I) comprising a cyclization of PerfluoroalkyI ketoesters (II) with hydrazines (lll).
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5.发明公开VERFAHREN ZUR HERSTELLUNG VON DITHIIN-TETRACARBOXIMIDEN 有权VERFAHREN ZUR HERSTELLUNG VON DITHININ-TARRARBOXIMIDEN
公开(公告)号：EP2558473A1
公开(公告)日：2013-02-20
申请号：EP11712882.7
申请日：2011-04-08
申请人： Bayer CropScience AG
发明人： HIMMLER, Thomas , ETZEL, Winfried , VOLZ, Frank
IPC分类号： C07D495/14 , C07D207/456
CPC分类号： C07D495/14 , C07D207/456
摘要： The invention relates to a novel method for producing dithiine tetracarboximides of the general formula (I), where R
1 and R
2 have the meanings given above, characterized in that succinic acid monoamides of the formula (VI), where R is R
1 or R
2 , is reacted with an excess of thionyl chloride, optionally in the presence of a thinner, the excess of thionyl chloride is subsequently removed, and the product mixture thus obtained is transformed into the dithiine tetracarboximide of the formula (I) in a second state in an organic solvent.摘要翻译： 本发明涉及用于生产通式（I）的二硫氨酸四甲酰亚胺的新方法，其中R 1和R 2具有以上给出的含义，其特征在于式（VI）的琥珀酸单酰胺，其中R是R 1或 R 2与过量的亚硫酰氯反应，任选在稀释剂存在下，随后除去过量的亚硫酰氯，并将由此获得的产物混合物在第二秒内转化成式（I）的二硫化四甲酰亚胺 在有机溶剂中进行。
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6.发明授权METHOD FOR THE PREPARATION OF PERFLUOROALKYL CONTAINING PYRAZOLES CARBOXYLATES 有权VERFAHREN ZUR HERSTELLUNG VON PERFLUORALKYLHALTIGEN PYRAZOLCARBYYYLATEN
公开(公告)号：EP2882717B1
公开(公告)日：2017-03-29
申请号：EP13745830.3
申请日：2013-08-02
申请人： Bayer CropScience AG
发明人： PAZENOK, Sergii , ETZEL, Winfried , LUI, Norbert , NEEFF, Arnd
IPC分类号： C07D231/16 , C07C17/00
CPC分类号： C07D231/16 , C07C17/00 , C07C67/343 , C07C69/716
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公开(公告)号：EP0865447B1
公开(公告)日：2003-02-12
申请号：EP96939113.5
申请日：1996-11-25
申请人： Bayer CropScience AG
发明人： ANKE, Heidrun , ETZEL, Winfried , GAU, Wolfgang , HAIN, Rüdiger , KILIAN, Michael , MAYER, Anke , STERNER, Olov
摘要： The invention relates to a novel cyclic peptide which is to be called Omphalotin. The invention also relates to a process for the preparation thereof by substantially microbiological means and the use thereof as a microbicide and pesticide, preferably for the control of animal pests, harmful fungi and bacteria.
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