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1. 发明申请

WO2006065659A3 INSECTICIDAL BIS(SUBSTITUTED PHENYL)-1-{[4-(SATURATED HETEROCYCLYL-SUBSTITUTED)PHENYLMETHYL]-(4-PIPERIDYL)}METHANE DERIVATIVES 审中-公开
标题翻译：杀虫剂BIS（取代的苯基）-1 - {[4-（饱和杂环取代的）苯基] - （4-哌啶基）}甲烷衍生物
公开(公告)号：WO2006065659A3
公开(公告)日：2006-08-24
申请号：PCT/US2005044666
申请日：2005-12-09
申请人： FMC CORP , LYGA JOHN W , ROSEN DAVID S , ZHANG Y LARRY , DING PING , HENRIE ROBERT N II , ZAWACKI FRANK J , HATCH CHARLES E III , ZHANG SHUNXIANG , GOUDAR JAIDEV S
发明人： LYGA JOHN W , ROSEN DAVID S , ZHANG Y LARRY , DING PING , HENRIE ROBERT N II , ZAWACKI FRANK J , HATCH CHARLES E III , ZHANG SHUNXIANG , GOUDAR JAIDEV S
IPC分类号： C07D211/00
CPC分类号： C07D405/10 , C07D401/10 , C07D405/14 , C07D409/10 , C07D409/14 , C07D411/10 , C07D413/10
摘要： It has now been found that certain novel bis(substituted phenyl)-1 {[4-(saturated heterocyclyl-substituted)phenylmethyl](4-piperidyl)}methane derivatives have provided unexpected insecticidal activity. These compounds are represented by formula (I); where R through R 15 , m, n, s, A, B, D and W are defined herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula (I), and optionally, an effective amount of at least one of a second compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present.
摘要翻译：现已发现某些新的双（取代苯基）-1 {[4-（饱和杂环基取代的）苯甲基]（4-哌啶基）}甲烷衍生物提供了意想不到的杀虫活性。这些化合物由式（I）表示; 其中R至R 15，...，M，n，s，A，B，D和W在本文中定义。此外，还公开了包含杀虫有效量的至少一种式（I）化合物和任选的有效量的至少一种第二化合物与至少一种与杀虫相容的载体的组合物; 以及控制昆虫的方法，包括将所述组合物施用于存在昆虫或预期存在的场所。

2. 发明申请

WO2007005455A2 IMPROVED PROCESS FOR PREPARING (DISUBSTITUTEDPROPENYL) PHENYLALKYL SUBSTITUTED HETEROCYCLES 审中-公开
标题翻译：制备（取代二苯基）苯基取代的杂环化合物的改进方法
公开(公告)号：WO2007005455A2
公开(公告)日：2007-01-11
申请号：PCT/US2006025144
申请日：2006-06-28
申请人： FMC CORP , GOUDAR JAIDEV S , HATCH CHARLES E III , WANG GUOZHI , POLSZ CRAIG A , PATERA RUSSELL
发明人： GOUDAR JAIDEV S , HATCH CHARLES E III , WANG GUOZHI , POLSZ CRAIG A , PATERA RUSSELL
IPC分类号： C07D403/02
CPC分类号： C07D213/64 , C07D307/58
摘要： An improved process is described for preparing (disubstitutedpropenyl) phenylalkyl substituted heterocycles. This improved process is focused on steps to produce key intermediates, namely compounds of formula (I): where R 3 , R 4 , R 5 and x are defined herein.
摘要翻译：描述了制备（二取代的丙烯基）苯基烷基取代的杂环的改进方法。这种改进的方法集中在产生关键中间体的步骤，即式（I）的化合物：其中R 3，R 4，R 5，和x在本文中定义。

3. 发明申请

WO2007005450A3 IMPROVED PROCESS FOR PREPARING (DISUBSTITUTEDPROPENYL) PHENYLALKYL SUBSTITUTED HETEROCYCLES 审中-公开
标题翻译：改进的制备（取代的苯丙基）苯基取代的杂环化合物的方法
公开(公告)号：WO2007005450A3
公开(公告)日：2007-03-29
申请号：PCT/US2006025130
申请日：2006-06-28
申请人： BAYER CROPSCIENCE AG , WANG GUOZHI , HATCH CHARLES E III , GOUDAR JAIDEV S , PATERA RUSSELL
发明人： WANG GUOZHI , HATCH CHARLES E III , GOUDAR JAIDEV S , PATERA RUSSELL
IPC分类号： A61K31/66 , A61K31/35 , A61K31/38 , A61K31/41 , A61K31/435 , C07D327/00 , C07F9/06 , C07F9/28
CPC分类号： C07F9/65517 , C07F9/582
摘要： An improved process is described for preparing (disubstitutedpropenyl) phenylalkyl substituted heterocycles. This improved process is focused on steps to produce key intermediates, namely compounds of formula I; where R 3 , R 4 , R 5 , R 7 , R 8 and x are defined herein.
摘要翻译：描述了制备（二取代的丙烯基）苯基烷基取代的杂环的改进方法。这一改进过程集中在生产关键中间体的步骤上，即式I化合物; 其中R 3，R 4，R 5，R 7，R 8，R 8，R 8，R 8，R 8，和x在此定义。

4. 发明申请

WO2007005454A3 IMPROVED PROCESS FOR PREPARING INSECTICIDAL (DISUBSTITUTEDPROPENYL) PHENYLALKYL SUBSTITUTED HETEROCYCLES 审中-公开
标题翻译：改进的制备杀虫剂（二丁基苯基）苯基烷基取代的杂环化合物的方法
公开(公告)号：WO2007005454A3
公开(公告)日：2007-05-03
申请号：PCT/US2006025143
申请日：2006-06-28
申请人： BAYER CROPSCIENCE AG , GOUDAR JAIDEV S , HATCH CHARLES E III , WANG GUOZHI , PATERA RUSSELL , POLSZ CRAIG A
发明人： GOUDAR JAIDEV S , HATCH CHARLES E III , WANG GUOZHI , PATERA RUSSELL , POLSZ CRAIG A
IPC分类号： C07D209/06 , C07D209/34
CPC分类号： C07D307/58 , C07D213/64
摘要： An improved process is described for preparing (disubstitutedpropenyl) phenylalkyl substituted heterocycles. This improved process is focused on steps to produce key intermediates, namely compounds of formula (I): where R 3 , R 4 , R 5 and x are defined herein.
摘要翻译：描述了制备（二取代的丙烯基）苯基烷基取代的杂环的改进方法。该改进方法集中于生产关键中间体的步骤，即式（I）的化合物：其中R 3，R 4，R 5，和x在此定义。

5. 发明申请

WO02056681A2 NOVEL INTERMEDIATES AND PROCESS TO PYRIMIDINEDIONE HERBICIDES 审中-公开
标题翻译：新型中间体和除草剂除草剂的方法
公开(公告)号：WO02056681A2
公开(公告)日：2002-07-25
申请号：PCT/US0150000
申请日：2001-10-19
申请人： FMC CORP , GOUDAR JAIDEV S , WANG GUOZHI
发明人： GOUDAR JAIDEV S , WANG GUOZHI
IPC分类号： C07C233/15 , C07C271/28 , C07D235/10 , C07D239/54 , C07D403/04 , A01N
CPC分类号： C07D239/54 , C07C233/15 , C07C271/28 , C07D235/10 , C07D403/04
摘要： A class of novel intermediates is described that have utility in processes for preparing uracil herbicides; wherein the novel intermediates are compounds of formula (A) which are cyclized with at least one cyclizing agent of formula (B) to provide a penultimate intermediate to, or a uracil herbicide, both of formula (I) where (X)n, Y, Z, R, R , R , R , and R are fully described herein. Preferred are those where Y and Z taken together are -N=C(R )-NR -, (X)n is 4-fluoro-6-chloro; R is hydrogen and methyl; R and R are trifluoromethyl, and R is hydrogen.
摘要翻译：描述了一类新型中间体，其用于制备尿嘧啶除草剂的方法; 其中所述新型中间体是式（A）的化合物，其与至少一种式（B）的环化剂环化以提供倒数第二中间体或式（I）的尿嘧啶除草剂，其中（X）n，Y ，Z，R，R 1，R 5，R 7和R 8在本文中被完整描述。优选Y和Z一起为-N = C（R 2）-NR 3 - ，（X）n为4-氟-6-氯的那些; R是氢和甲基; R 1和R 2是三氟甲基，R 3是氢。

6. 发明申请

WO0127092A3 PROCESS TO PREPARE ARYLTRIAZOLINONES AND NOVEL INTERMEDIATES THERETO 审中-公开
标题翻译：制备芳基三唑啉酮及其中间体的新方法
公开(公告)号：WO0127092A3
公开(公告)日：2001-10-25
申请号：PCT/US0028240
申请日：2000-10-12
申请人： FMC CORP
发明人： GOUDAR JAIDEV S
IPC分类号： C07B61/00 , C07C257/02 , C07C257/22 , C07D249/12
CPC分类号： C07C257/22 , C07D249/12
摘要： A process is described for preparing 1-aryltriazolinones of formula (I) useful in the production of commercial herbicides, by: i) carbonylating an amidrazone of formula (A) with one or more carbonylating agent, or ii) condensing a hydrazonoyl derivative of formula (A) with one or more ring-forming agent in formula (A), where W, X, Y, Z, and R are fully described herein. Preferred are those where W is halogen or -NHR where R is hydrogen or haloalkyl; X and Y are independently selected from hydrogen, chloro, or fluoro; Z is hydrogen, bromo, iodo, nitro, amino, or methylsulfonylamino; and R is methyl. Certain compounds of formula (A) are novel compositions of matter. The process as described herein has utility in providing compounds of formula (I) in unexpectedly high yield and purity.
摘要翻译：描述了用于制备可用于生产商业除草剂的式（I）的1-芳基三唑啉酮的方法，其通过：i）用一种或多种羰基化剂将式（A）的氨基腙羰基化，或者ii）将式（I）的亚肼基衍生物（A）与式（A）中的一种或多种成环剂反应，其中W，X，Y，Z和R 1在本文中完全描述。优选W为卤素或-NHR（其中R为氢或卤代烷基）的那些; X和Y独立地选自氢，氯或氟; Z是氢，溴，碘，硝基，氨基或甲基磺酰基氨基; 并且R 1是甲基。某些式（A）化合物是新颖的物质组合物。如本文所述的方法可用于提供意想不到的高收率和纯度的式（I）化合物。

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