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1. 发明授权

US4639527A Process for the preparation of .beta.-hydroxyethyl-(1,2,4-triazole) derivatives 失效
标题翻译：制备β-羟乙基 - （1,2,4-三唑）衍生物的方法
公开(公告)号：US4639527A
公开(公告)日：1987-01-27
申请号：US672553
申请日：1984-11-19
申请人： Reinhard Lantzsch , Karl-Julius Reubke
发明人： Reinhard Lantzsch , Karl-Julius Reubke
IPC分类号： B01J31/00 , C07B61/00 , C07D249/08 , C07D521/00
CPC分类号： C07D231/12 , C07D233/56 , C07D249/08
摘要： The known .beta.-hydroxyethyl-(1,2,4-triazole) derivatives of the formula ##STR1## in which R.sup.1 represents alkyl, halogenoalkyl, alkenyl, alkinyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted aralkenyl or an optionally substituted heterocyclic radical andR.sup.2 represents hydrogen, alkyl, halogenoalkyl, alkenyl, alkinyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted aralkenyl or an optionally substituted heterocyclic radical,are prepared by a new process, which comprises stirring a .beta.-hydroxyethyl-(1,3,4-triazole) derivative of the formula ##STR2## in which R.sup.1 and R.sup.2 have the abovementioned meanings, in the presence of a base and in the presence of an aprotic, dipolar diluent.
摘要翻译：已知的式（I）的β-羟基乙基 - （1,2,4-三唑）衍生物，其中R 1表示烷基，卤代烷基，烯基，炔基，任选取代的环烷基，任选取代的环烯基，任选取代的芳基，任选地取代的芳烷基，任选取代的芳烯基或任选取代的杂环基，R 2表示氢，烷基，卤代烷基，烯基，炔基，任选取代的环烷基，任选取代的环烯基，任选取代的芳基，任选取代的芳烷基，任选取代的芳烯基或任选取代的杂环基通过新方法制备，其包括在存在下述步骤的同时搅拌式（II）的β-羟乙基 - （1,3,4-三唑）衍生物，其中R 1和R 2具有上述含义在非质子偶极稀释剂的存在下。

2. 发明授权

US4719307A Process for the preparation of .beta.-hydroxyethyl-(1,2,4-triazole) derivatives 失效
标题翻译：制备β-羟乙基 - （1,2,4-三唑）衍生物的方法
公开(公告)号：US4719307A
公开(公告)日：1988-01-12
申请号：US916077
申请日：1986-10-06
申请人： Reinhard Lantzsch , Karl-Julius Reubke
发明人： Reinhard Lantzsch , Karl-Julius Reubke
IPC分类号： B01J31/00 , C07B61/00 , C07D249/08 , C07D521/00
CPC分类号： C07D231/12 , C07D233/56 , C07D249/08
摘要： The known .beta.-hydroxyethyl-(1,2,4-triazole) derivatives of the formula ##STR1## in which R.sup.1 represents alkyl, halogenoalkyl, alkenyl, alkinyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted aralkenyl or an optionally substituted heterocyclic radical andR.sup.2 represents hydrogen, alkyl, halogenoalkyl, alkenyl, alkinyl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted aralkenyl or an optionally substituted heterocyclic radical,are prepared by a new process, which comprises stirring a .beta.-hydroxyethyl-(1,3,4-triazole) derivative of the formula ##STR2## in which R.sup.1 and R.sup.2 have the abovementional meanings, in the presence of a base and in the presence of an aprotic, dipolar diluent.
摘要翻译：已知的式（I）的β-羟基乙基 - （1,2,4-三唑）衍生物，其中R 1表示烷基，卤代烷基，烯基，炔基，任选取代的环烷基，任选取代的环烯基，任选取代的芳基，任选地取代的芳烷基，任选取代的芳烯基或任选取代的杂环基，R 2表示氢，烷基，卤代烷基，烯基，炔基，任选取代的环烷基，任选取代的环烯基，任选取代的芳基，任选取代的芳烷基，任选取代的芳烯基或任选取代的杂环基通过新方法制备，其包括在存在下述步骤的情况下搅拌式（II）的β-羟乙基 - （1,3,4-三唑）衍生物，其中R 1和R 2具有上述含义在非质子偶极稀释剂的存在下。

3. 发明授权

US4626594A Process for the preparation of beta-hydroxyethyl-(1,2,4-triazole) derivatives 失效
标题翻译： β-羟乙基 - （1,2,4-三唑）衍生物的制备方法
公开(公告)号：US4626594A
公开(公告)日：1986-12-02
申请号：US672767
申请日：1984-11-19
申请人： Reinhard Lantzsch , Karl-Julius Reubke
发明人： Reinhard Lantzsch , Karl-Julius Reubke
IPC分类号： B01J31/00 , C07B61/00 , C07D249/08 , C07D521/00
CPC分类号： C07D231/12 , C07D233/56 , C07D249/08
摘要： Known .beta.-hydroxyethyl-(1,2,4-triazole) derivatives of the formula ##STR1## in which R represents alkyl, halogenoalkyl, optionally substituted cycloalkyl or optionally substituted phenyl,Z represents halogen, alkyl, cycloalkyl, alkoxy, alkylthio, halogenoalkyl, halogenoalkoxy, halogenoalkylthio, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylalkyl or optionally substituted phenylalkoxy andm represents the number 0, 1, 2 or 3,are prepared by a new process, which comprises reacting oxiranes of the formula ##STR2## in which R, Z and m have the abovementioned meaning, with 1,2,4-triazole of the formula ##STR3## in the presence of a cylcic amid of the formula ##STR4## in which R.sup.1 represents alkyl with 1 to 4 carbon atoms andn represents the number 3, 4 or 5,as diluent, and in the presence of a base.
摘要翻译：已知的式（I）的β-羟乙基 - （1,2,4-三唑）衍生物，其中R表示烷基，卤代烷基，任选取代的环烷基或任选取代的苯基，Z表示卤素，烷基，环烷基，烷氧基，烷基硫代，卤代烷基，卤代烷氧基，卤代烷硫基，任选取代的苯基，任选取代的苯氧基，任选取代的苯基烷基或任选取代的苯基烷氧基，m代表数字0,1,2或3，通过新方法制备，其包括使式在其中R，Z和m具有上述含义的式（II）中，与式（III）的1,2,4-三唑在式（IV）的酰胺存在下反应），其中R 1表示具有1至4个碳原子的烷基，n表示3,4或5个作为稀释剂，并且在碱的存在下。

4. 发明授权

US07897803B2 Cis-alkoxy-substituted spirocyclic 1H-pyrrolidine-2,4-dione derivatives serving as pesticides 有权
标题翻译：用作农药的顺式 - 烷氧基取代的螺环-1H-吡咯烷-2,4-二酮衍生物
公开(公告)号：US07897803B2
公开(公告)日：2011-03-01
申请号：US12615466
申请日：2009-11-10
申请人： Thomas Himmler , Reiner Fischer , Bernd Gallenkamp , Hans-Joachim Knops , Lubbertus Mulder , Reinhard Lantzsch , Christoph Erdelen , Angelika Lubos-Erdelen, legal representative , Jorg Konze , Ralf Nauen , Olga Malsam , Christian Arnold
发明人： Thomas Himmler , Reiner Fischer , Bernd Gallenkamp , Hans-Joachim Knops , Lubbertus Mulder , Reinhard Lantzsch , Christoph Erdelen , Jorg Konze , Ralf Nauen , Olga Malsam , Christian Arnold
IPC分类号： 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 1 H-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如披露

5. 发明申请

US20060122426A1 Method for producing phthalic acid dichloride 审中-公开
标题翻译：邻苯二甲酸二氯化物的制备方法
公开(公告)号：US20060122426A1
公开(公告)日：2006-06-08
申请号：US10524748
申请日：2003-08-06
申请人： Jorn Stolting , Reinhard Lantzsch
发明人： Jorn Stolting , Reinhard Lantzsch
IPC分类号： C07C51/58
CPC分类号： C07C51/60 , C07C63/22
摘要： The invention relates to a novel method for producing phthalic acid dichloride (benzene-1,2-dicarbonylchloride) from phthalic anhydride by reaction with phosgene in the presence of N,N-dialkylformamides.
摘要翻译：本发明涉及在N，N-二烷基甲酰胺的存在下与邻苯二甲酸酐反应生成邻苯二甲酸二氯（苯-1,2-二羰基氯）的新方法。

6. 发明授权

US06730799B2 Process for preparing 3-(1-hydroxyphenyl-1-alkoximinomethyl)dioxazines 失效
标题翻译：制备3-（1-羟基苯基-1-肟基甲基）二恶嗪的方法
公开(公告)号：US06730799B2
公开(公告)日：2004-05-04
申请号：US10162947
申请日：2002-06-05
申请人： Herbert Gayer , Bernd Gallenkamp , Peter Gerdes , Ulrich Heinemann , Bernd-Wieland Krüger , Reinhard Lantzsch , Thomas Seitz , Uwe Stelzer
发明人： Herbert Gayer , Bernd Gallenkamp , Peter Gerdes , Ulrich Heinemann , Bernd-Wieland Krüger , Reinhard Lantzsch , Thomas Seitz , Uwe Stelzer
IPC分类号： C07D30777
CPC分类号： C07D273/00 , C07D307/82 , C07D307/83 , C07D407/12
摘要： The present invention relates to a plurality of novel processes and novel intermediates for preparing 3-(1-hydroxyphenyl-1-alkoximinomethyl)dioxazines, which are known as intermediates for preparing compounds having fungicidal properties (WO 95-04728).
摘要翻译：本发明涉及用于制备3-（1-羟基苯基-1-肟基甲基）二恶嗪的多种新方法和新型中间体，其被称为制备具有杀真菌性质的化合物的中间体（WO 95-04728）。

7. 发明授权

US06479675B1 Processes for preparing 3-(1-hydroxyphenyl-1-alkoximinomethyl) dioxazines 有权
标题翻译：制备3-（1-羟基苯基-1-肟基甲基）二恶嗪的方法
公开(公告)号：US06479675B1
公开(公告)日：2002-11-12
申请号：US09619141
申请日：2000-07-19
申请人： Herbert Gayer , Bernd Gallenkamp , Peter Gerdes , Ulrich Heinemann , Bernd-Wieland Krüger , Reinhard Lantzsch , Thomas Seitz , Uwe Stelzer
发明人： Herbert Gayer , Bernd Gallenkamp , Peter Gerdes , Ulrich Heinemann , Bernd-Wieland Krüger , Reinhard Lantzsch , Thomas Seitz , Uwe Stelzer
IPC分类号： C07D30778
CPC分类号： C07D273/00 , C07D307/82 , C07D307/83 , C07D407/12
摘要： The present invention relates to a plurality of novel processes and novel intermediates for preparing 3-(1-hydroxyphenyl-1-alkoximinomethyl)dioxazines, which are known as intermediates for preparing compounds having fungicidal properties (WO 95-04728).
摘要翻译：本发明涉及用于制备3-（1-羟基苯基-1-肟基甲基）二恶嗪的多种新方法和新型中间体，其被称为制备具有杀真菌性质的化合物的中间体（WO 95-04728）。

8. 发明授权

US06306855B1 Fluoromethoximino compounds 失效
标题翻译：荧光素肟化合物
公开(公告)号：US06306855B1
公开(公告)日：2001-10-23
申请号：US09445084
申请日：1999-12-02
申请人： Ulrich Heinemann , Herbert Gayer , Peter Gerdes , Albrecht Marhold , Uwe Stelzer , Reinhard Lantzsch , Ralf Tiemann , Klaus Stenzel , Astrid Mauler-Machnik , Stefan Dutzmann , Martin Kugler , Hans-Ulrich Buschhaus
发明人： Ulrich Heinemann , Herbert Gayer , Peter Gerdes , Albrecht Marhold , Uwe Stelzer , Reinhard Lantzsch , Ralf Tiemann , Klaus Stenzel , Astrid Mauler-Machnik , Stefan Dutzmann , Martin Kugler , Hans-Ulrich Buschhaus
IPC分类号： C07D25112
CPC分类号： C07D285/08 , A01N43/54 , A01N43/82 , C07C251/52 , C07D239/34 , C07D239/52 , C07D251/20 , C07D271/07
摘要： The invention relates to novel fluoromethoximino compounds, to a process for their preparation and to their use as pesticides, and also to novel intermediates and to a plurality of processes for their preparation.
摘要翻译：本发明涉及新的荧光肟化合物，其制备方法及其作为农药的用途，以及新颖的中间体和多种制备方法。

9. 发明授权

US6166214A Process for preparing pyridylmethyl isothiocyanates 有权
标题翻译：制备吡啶基甲基异硫氰酸酯的方法
公开(公告)号：US6166214A
公开(公告)日：2000-12-26
申请号：US298593
申请日：1999-04-23
申请人： Klaus Wagner , Reinhard Lantzsch
发明人： Klaus Wagner , Reinhard Lantzsch
IPC分类号： C07D213/36 , C07D213/40 , C07D213/61 , C07D249/53
CPC分类号： C07D213/40 , C07D213/61
摘要： The present invention relates to a novel process for preparing pyridylmethyl isothiocyanates of the formula (I) ##STR1## in which R.sup.1 represents halogen or C.sub.1 -C.sub.4 -alkyl, characterized in that in a first step, amines of the formula (II) ##STR2## in which R.sup.1 is as defined above, are reacted with xanthogenates of the formula (III)R.sup.2 O--CS--S.sup..crclbar. M.sup..sym. (III)in whichR.sup.2 represents C.sub.1 -C.sub.4 -alkyl, preferably methyl or ethyl andM represents an alkali metal, preferably sodium and potassium or represents ammonium,if appropriate in the presence of a diluent, and in a second step, the resulting novel dithiocarbamates of the formula (IV) ##STR3## in which R.sup.1 and M are each as defined above, are oxidized, if appropriate in the presence of a diluent, to give the isothiocyanates of the formula (I).
摘要翻译：本发明涉及一种制备式（I）的吡啶基甲基异硫氰酸酯的新方法，其中R 1表示卤素或C 1 -C 4 - 烷基，其特征在于在第一步中，式（II）的胺其中R1为与式（III）R2O-CS-S（ - ）M（+）（III）的黄原酸酯反应，其中R 2表示C 1 -C 4烷基，优选甲基或乙基，M表示碱金属，优选钠和钾，或代表铵，如果合适，在稀释剂存在下，并且在第二步中，得到的式（Ⅳ）的新型二硫代氨基甲酸酯，其中R 1和M如上所定义，如果适用，则在存在稀释剂，得到式（I）的异硫氰酸酯。

10. 发明授权

US6118031A Process for producing substituted arylpyrazoles 失效
标题翻译：制备取代芳基吡唑的方法
公开(公告)号：US6118031A
公开(公告)日：2000-09-12
申请号：US369620
申请日：1999-08-06
申请人： Reinhard Lantzsch , Thomas Himmler , Albrecht Marhold
发明人： Reinhard Lantzsch , Thomas Himmler , Albrecht Marhold
IPC分类号： C07C17/093 , C07C17/12 , C07C17/361 , C07C25/02 , C07C25/13 , C07C25/24 , C07C33/48 , C07C45/45 , C07C49/235 , C07C255/49 , C07D231/12 , C07F7/08
CPC分类号： C07D231/12 , C07C17/12 , C07C17/361 , C07C25/13 , C07C33/48 , C07C45/455 , C07C49/235 , C07F7/0818
摘要： The invention relates to a process for preparing substituted arylpyrazoles of the general formula (I) ##STR1## in which R.sup.1, R.sup.2, R.sup.3 and R .sup.4 are each as defined in the description, and to novel intermediates for preparing these arylpyrazoles.
摘要翻译：本发明涉及一种制备通式（I）的取代芳基吡唑的方法，其中R 1，R 2，R 3和R 4各自如说明书中所定义，以及制备这些芳基吡唑的新中间体。

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