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41. 发明申请

US20100056598A1 CIS-ALKOXY-SUBSTITUTED SPIROCYCLIC 1H-PYRROLIDINE-2,4-DIONE DERIVATIVES SERVING AS PESTICIDES 有权
标题翻译：作为杀虫剂服用的独特的烷基取代的螺环形的1H-吡咯烷-2,4-二酮衍生物
公开(公告)号：US20100056598A1
公开(公告)日：2010-03-04
申请号：US12615466
申请日：2009-11-10
申请人： Thomas Himmler , Reiner Fisher , Bernd Gallenkamp , Hans-Joachim Knops , Lubbertus Mulder , Reinhard Lantzsch , Christoph Erdelen , Angelika Lubos-Erdelen , Jorg Konze , Ralf Nauen , Olga Malsam , Christian Arnold
发明人： Thomas Himmler , Reiner Fisher , Bernd Gallenkamp , Hans-Joachim Knops , Lubbertus Mulder , Reinhard Lantzsch , Christoph Erdelen , Angelika Lubos-Erdelen , Jorg Konze , Ralf Nauen , Olga Malsam , Christian Arnold
IPC分类号： A01N43/38 , C07D209/54 , C07C229/54
CPC分类号： A01N43/38 , A01N47/06 , C07D207/38
摘要： The invention relates to a plurality of processes for the preparation of novel cis-alkoxy-substituted spirocyclic 1H-pyrrolidine-2,4-dione derivatives of the formula (I) in which A, G, X and Y are as defined in the disclosure.
摘要翻译：本发明涉及制备式（I）的新型顺式 - 烷氧基取代的螺环-1H-吡咯烷-2,4-二酮衍生物的多种方法，其中A，G，X和Y如本公开所定义。

42. 发明申请

US20080194835A1 Methods for the Manufacture of Biphenyl Amines 失效
标题翻译：联苯胺制备方法
公开(公告)号：US20080194835A1
公开(公告)日：2008-08-14
申请号：US11574088
申请日：2005-08-13
申请人： Wolfgang Jorges , Jens-Dietmar Heinrich , Reinhard Lantzsch
发明人： Wolfgang Jorges , Jens-Dietmar Heinrich , Reinhard Lantzsch
IPC分类号： C07D231/44 , C07C211/46
CPC分类号： C07C233/15 , C07C209/62 , C07C211/52 , C07C231/12 , C07C233/25 , C07D231/14
摘要： The present invention relates to a new method for the manufacture of substituted biphenyl amines, new intermediate products and their manufacture, as well as a method for the manufacture of fungicidally active carboxamides.
摘要翻译：本发明涉及用于制备取代的联苯胺，新的中间产物及其制备的新方法，以及制备杀真菌活性的羧酰胺的方法。

43. 发明申请

US20080039663A1 Method For Producing 3-Halophthalic Acid Dichlorides 审中-公开
标题翻译：生产3-卤代邻苯二甲酸二氯化物的方法
公开(公告)号：US20080039663A1
公开(公告)日：2008-02-14
申请号：US11792113
申请日：2005-11-23
申请人： Jorn Stolting , Reinhard Lantzsch , Sergiy Pazenok
发明人： Jorn Stolting , Reinhard Lantzsch , Sergiy Pazenok
IPC分类号： C07F15/00
CPC分类号： C07C51/60 , C07C63/22
摘要： The invention relates to a novel process for preparing 3-halophthaloyl chlorides (3-halobenzene-1,2-dicarbonyl chlorides) from the corresponding 3-halophthalic anhydrides by reacting with phosgene in the presence of an N,N-dialkylformamide.
摘要翻译：本发明涉及通过在N，N-二烷基甲酰胺的存在下与光气反应从相应的3-卤代邻苯二甲酸酐制备3-卤代邻苯二酰氯（3-卤代苯-1,2-二羰基氯）的新方法。

44. 发明申请

US20060276656A1 Method for the production of fluoromethyl-substituted heterocycles 有权
标题翻译：制备氟甲基取代的杂环的方法
公开(公告)号：US20060276656A1
公开(公告)日：2006-12-07
申请号：US10576742
申请日：2004-10-19
申请人： Reinhard Lantzsch , Sergiy Pazenok , Frank Memmel
发明人： Reinhard Lantzsch , Sergiy Pazenok , Frank Memmel
IPC分类号： C07D277/24 , C07D231/10
CPC分类号： C07D263/34 , C07D231/14 , C07D277/30
摘要： The present invention relates to a process for preparing fluoromethyl-substituted heterocycles of the formula (I) in which R1, R2, R3 and A are each as defined in the disclosure, by fluorinating the corresponding chloromethyl-substituted precursors.
摘要翻译：本发明涉及制备式（I）的氟甲基取代的杂环的方法，其中R 1，R 2，R 3，和A各自如本公开所定义，通过氟化相应的氯甲基取代的前体。

45. 发明申请

US20060252944A1 Method for producing 2-dihaloacyl-3-amino-acrylic acid esters and 3-dihalomethyl pyrazole-4-carboxylic acid esters 有权
标题翻译： 2-二卤代-3-氨基丙烯酸酯和3-二卤甲基吡唑-4-羧酸酯的制备方法
公开(公告)号：US20060252944A1
公开(公告)日：2006-11-09
申请号：US10576059
申请日：2004-10-12
申请人： Reinhard Lantzsch , Wolfgang Jorges , Sergiy Pazenok
发明人： Reinhard Lantzsch , Wolfgang Jorges , Sergiy Pazenok
IPC分类号： C07D231/02 , C07C227/16
CPC分类号： C07C229/30 , C07D231/14
摘要： The present invention relates to a process for preparing 2-dihaloacyl-3-aminoacrylic esters of the formula (I) characterized in that acid halides of the formula (II) are reacted with dialkylaminoacrylic esters of the formula (III) in which R, R1, R2, X1, X2 and Hal are each as defined in the description in a water-immiscible organic solvent in the presence of a base, to the novel 2-dihaloacyl-3-aminoacrylic esters of the formula (I) themselves, to their use for preparing 3-dihalomethylpyrazoles, to a process for preparing 3-dihalomethylpyrazoles, and also to novel 3-dihalomethylpyrazoles.
摘要翻译：本发明涉及制备式（I）的2-二卤代-3-氨基丙烯酸酯的方法，其特征在于式（II）的酰卤与式（III）的二烷基氨基丙烯酸酯反应，其中R，R R 1，R 2，X 1，X 2和X 2各自如在描述中所定义的在水中在碱的存在下，与式（I）本身的新型2-二卤代酰基-3-氨基丙烯酸酯，其用于制备3-二卤代甲基吡唑的方法相比，可用于制备3-二卤代甲基吡唑的方法，以及到新的3-二卤代甲基吡唑。

46. 发明授权

US06476224B2 Method for producing ar(alk)yluraciles, novel corresponding intermediate products and method for producing said intermediate products 失效
标题翻译：制备芳（alk）基脲的方法，新型相应的中间产物以及生产所述中间产物的方法
公开(公告)号：US06476224B2
公开(公告)日：2002-11-05
申请号：US09783838
申请日：2001-02-14
申请人： Bernd Gallenkamp , Reinhard Lantzsch , Lothar Rohe , Lubbertus Mulder
发明人： Bernd Gallenkamp , Reinhard Lantzsch , Lothar Rohe , Lubbertus Mulder
IPC分类号： C07D23954
CPC分类号： C07D239/47 , C07C275/16 , C07C275/24 , C07D239/54 , C07D239/553
摘要： The invention relates to a process for preparing ar(alk)yluracils of the general formula (I) in which A represents a single bond or represents alkanedlyl, Ar represents optionally substituted aryl, R1 represents optionally substituted alkyl and R2 represents hydrogen, halogen or alkyl, and to novel intermediates for this purpose and to processes for their preparation.
摘要翻译：本发明涉及一种制备通式（I）的芳（alk）基尿嘧啶的方法，其中A代表单键或代表烷基，Ar表示任意取代的芳基，R 1表示任选取代的烷基，R 2表示氢，卤素或烷基，用于此目的的新型中间体及其制备方法。

47. 发明授权

US06462205B1 Method of preparing benzofurandione oxime derivatives 失效
标题翻译：苯并呋喃二酮肟衍生物的制备方法
公开(公告)号：US06462205B1
公开(公告)日：2002-10-08
申请号：US09937420
申请日：2001-09-26
申请人： Walter Hübsch , Lubbertus Mulder , Bernd Gallenkamp , Herbert Gayer , Reinhard Lantzsch
发明人： Walter Hübsch , Lubbertus Mulder , Bernd Gallenkamp , Herbert Gayer , Reinhard Lantzsch
IPC分类号： C07D30700
CPC分类号： C07D307/82 , C07D307/83
摘要： The present invention relates to a novel process for preparing benzofurandioneoxime derivatives by reacting benzofurandioneoxime derivatives with acids.
摘要翻译：本发明涉及一种通过使苯并呋喃并偕酮肟衍生物与酸反应来制备苯并呋喃并靛红衍生物的新方法。

48. 发明授权

US06271389B1 Method for producing triazolinethione derivatives 有权
标题翻译：三唑啉酮衍生物的制备方法
公开(公告)号：US06271389B1
公开(公告)日：2001-08-07
申请号：US09509889
申请日：2000-04-03
申请人： Reinhard Lantzsch , Manfred Jautelat , Achim Hupperts , David Erdman
发明人： Reinhard Lantzsch , Manfred Jautelat , Achim Hupperts , David Erdman
IPC分类号： C07D24912
CPC分类号： C07D249/12
摘要： According to a novel process, it is possible to prepare triazolinethione derivatives of the formula in which R1 and R2 are each as defined in the description by a) reacting hydrazine derivatives of the formula with carbonyl compounds of the formula in which R3 and R4 are each as defined in the description with potassium thiocyanate, sodium thiocyanate or ammonium thiocyanate, if appropriate in the presence of a diluent and if appropriate in the presence of an acid, and b) reacting the resulting triazolidinethione derivatives of the formula with formic acid, if appropriate in the presence of a catalyst and if appropriate in the presence of a diluent. The triazolidinethione derivatives of the formula (V) are novel.
摘要翻译：根据一个新方法，可以制备式（Ⅲ）的三唑啉酮衍生物，其中R1和R2各自如说明书中所定义.a）使下式的肼衍生物与下式的羰基化合物反应：其中R 3和R 4各自如如果在稀释剂存在下和适当的情况下在酸存在下，硫氰酸钠，硫氰酸钠或硫氰酸铵的描述，以及b）如果合适的话，在酸的存在下，将所得到的式I的三唑烷硫酮衍生物与甲酸反应，催化剂，如果合适，则在稀释剂存在下。式（Ⅴ）的三唑烷酮二酮衍生物是新颖的。

49. 发明授权

US06204397B1 Process for the preparation of 3-substituted 4-cyano-pyrrole compounds 失效
标题翻译：制备3-取代的4-氰基 - 吡咯化合物的方法
公开(公告)号：US06204397B1
公开(公告)日：2001-03-20
申请号：US08086602
申请日：1993-07-01
申请人： Peter C. Knüppel , Reinhard Lantzsch , Klaus Jelich , Peter Andres , Albrecht Marhold
发明人： Peter C. Knüppel , Reinhard Lantzsch , Klaus Jelich , Peter Andres , Albrecht Marhold
IPC分类号： C07D31752
CPC分类号： C07D317/46
摘要： A process for the preparation of 3-substituted 4-cyano-pyrrole compounds of the formula (I) in which Ar has the meaning given in the description, by reaction in a 1st stage of bromides (II) Ar—Br (II) with acrylonitrile in the presence of a solvent and a suitable reaction auxiliary to give acrylonitrile derivatives (III) Ar—CH═CH—CN (III) and in a 2nd stage with a phenylsulphonylmethyl isocyanide (IV) Ph—SO2—CH2—CN (IV) in the presence of a solvent and optionally in the presence of a suitable reaction auxiliary, characterised in that the the 1st stage is carried out in the presence of a palladium catalyst and the 2nd stage in the presence of a 1.2- to 1.8-fold molar excess of alkali metal alcoholate or alkali metal hydroxide.
摘要翻译：制备式（I）的3-取代的4-氰基 - 吡咯化合物的方法，其中Ar具有在描述中给出的含义，通过在第一阶段的溴化物（II）与丙烯腈在溶剂存在下反应和适当的反应助剂，在溶剂存在下，任选地在合适的反应助剂的存在下，在丙烯腈衍生物（III）中和在第二阶段中与苯基磺酰基甲基异氰化物（IV）反应，其特征在于携带第一阶段在钯催化剂存在下进行，第二阶段在1.2至1.8倍摩尔过量的碱金属醇化物或碱金属氢氧化物的存在下进行。

50. 发明授权

US06172093B2 Substituted biphenyloxazolines 失效
标题翻译：取代的联苯并恶唑啉
公开(公告)号：US06172093B2
公开(公告)日：2001-01-09
申请号：US08511212
申请日：1995-08-04
申请人： Reinhard Lantzsch , Albrecht Marhold , Wolfgang Kr{umlaut over (a)}mer , Christoph Erdelen , Ulrike Wachendorff-Neumann , Andreas Turberg , Norbert Mencke
发明人： Reinhard Lantzsch , Albrecht Marhold , Wolfgang Kr{umlaut over (a)}mer , Christoph Erdelen , Ulrike Wachendorff-Neumann , Andreas Turberg , Norbert Mencke
IPC分类号： A01N4376
CPC分类号： C07D263/14 , A01N43/76 , C07C43/225 , C07C45/46 , C07C45/63 , C07C45/64 , C07C45/71 , C07C217/64 , C07C233/73 , C07C233/87 , C07C251/44 , C07C49/84
摘要： New pesticidal substituted biphenytoxazolines of the formula (I) in which A, B, X, m and n have the meanings stated in the description, and new intermediates therefor.
摘要翻译：其中A，B，X，m和n具有说明书中所述含义的式（I）的新的杀虫剂取代的联苯并恶唑啉及其新的中间体。

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