专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

1. 发明授权

US4762830A 5-(azolyloxyphenylcarbamoyl)barbituric acid derivatives as anthelmintics 失效
标题翻译： 5-（阿唑酰氧基苯基氨基甲酰基）巴比妥酸衍生物作为驱肠虫剂
公开(公告)号：US4762830A
公开(公告)日：1988-08-09
申请号：US830430
申请日：1986-02-13
申请人： Elmar Sturm , Jean J. Gallay , Haukur Kristinsson , Georg Pissiotas
发明人： Elmar Sturm , Jean J. Gallay , Haukur Kristinsson , Georg Pissiotas
IPC分类号： C07D263/58 , A61K31/496 , A61K31/515 , A61P33/10 , C07D233/70 , C07D235/26 , C07D239/62 , C07D239/66 , C07D249/08 , C07D249/12 , C07D271/06 , C07D271/10 , C07D271/113 , C07D277/24 , C07D277/34 , C07D277/58 , C07D277/68 , C07D285/08 , C07D285/12 , C07D285/13 , C07D403/12 , C07D413/12 , C07D417/12 , A61K31/505 , C07D403/10
CPC分类号： C07D271/113 , C07D233/70 , C07D239/62 , C07D239/66 , C07D249/12 , C07D277/34 , C07D277/58 , C07D277/68 , C07D285/08 , C07D285/13 , C07D413/12 , C07D417/12
摘要： The invention relates to novel 5-(azolyloxyphenylcarbamoyl)barbituric acid derivatives of the general formula I ##STR1## wherein X is oxygen or sulfur;R.sub.1 is C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, C.sub.3 -C.sub.6 cycloalkyl or allyl;R.sub.2 is C.sub.1 -C.sub.6 alkyl or allyl;R.sub.3 is an unsubstituted or substituted five-membered azole ring which is bound through carbon and is selected from the group consisting of benzimadazole, benzoxazole, benzothiazole, imidazole, oxazole, thiazole, oxadiazole, thiadiazole and triazole; andR.sub.4 and R.sub.5 are each independently of the other hydrogen, C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 haloalkyl, C.sub.1 -C.sub.6 alkoxy or C.sub.1 -C.sub.6 haloalkoxy;and to the tautomers and salts thereof, as anthelmintic compounds. Together with suitable carriers and further assistants, these compounds may be used in particular for controlling helminths which are parasites of animals.
摘要翻译：本发明涉及通式I（I）的新的5-（azolyloxyphenylcarbamoyl）巴比土酸衍生物，其中X是氧或硫; R1是C1-C6烷基，C1-C6烷氧基，C3-C6环烷基或烯丙基; R2是C1-C6烷基或烯丙基; R3是通过碳结合的未取代或取代的五元唑环，选自苯并咪唑，苯并恶唑，苯并噻唑，咪唑，恶唑，噻唑，恶二唑，噻二唑和三唑; 并且R 4和R 5各自独立地为另一个氢，C 1 -C 6烷基，C 1 -C 6卤代烷基，C 1 -C 6烷氧基或C 1 -C 6卤代烷氧基; 和其互变异构体和盐，作为驱肠剂化合物。与合适的载体和进一步助剂一起，这些化合物可特别用于控制作为动物寄生虫的蠕虫。

2. 发明授权

US4364769A 1,3,4-Thiadiazolyloxyphenylureas 失效
标题翻译： 1,3,4-噻二唑基氧基苯基脲
公开(公告)号：US4364769A
公开(公告)日：1982-12-21
申请号：US166679
申请日：1980-07-07
申请人： Georg Pissiotas , Otto Rohr , Haukur Kristinsson
发明人： Georg Pissiotas , Otto Rohr , Haukur Kristinsson
IPC分类号： A01N47/30 , A01N47/32 , A01N47/38 , C07D285/12 , C07D285/125 , C07D285/13 , A01N47/28
CPC分类号： C07D285/13 , A01N47/30 , A01N47/32 , A01N47/38 , C07D285/125
摘要： The invention relates to novel 1,3,4-thiadiazolyloxyphenylureas which possess herbicidal properties and which have good selectivity in different crops of cultivated plants. The novel phenylureas have the general formula I ##STR1## wherein X is hydrogen, halogen or trifluoromethyl,Y is hydrogen, C.sub.1 -C.sub.6 alkyl which can be interrupted by oxygen or substituted by halogen or cyano; C.sub.3 -C.sub.6 cycloalkyl, cyclopropylmethyl, phenyl which is unsubstituted or substituted by chlorine or C.sub.1 -C.sub.4 alkyl; or is C.sub.1 -C.sub.4 alkylthio, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkylsulfinyl or C.sub.1 -C.sub.4 alkylsulfonyl, or a sulfamoyl group --SO.sub.2 NR.sub.2 R.sub.3,R.sub.1 is hydrogen or C.sub.1 -C.sub.4 alkyl,R.sub.2 is hydrogen, C.sub.1 -C.sub.6 alkyl which can be interrupted by oxygen or substituted by halogen or cyano, or is C.sub.3 -C.sub.6 alkenyl or C.sub.3 -C.sub.6 alkynyl, or C.sub.3 -C.sub.6 cycloalkyl, has the same meaning as R.sub.2 or is C.sub.1 -C.sub.6 alkoxy, orR.sub.2 and R.sub.3, together with the nitrogen atom to which they are attached, can also form a 5- or 6-membered heterocyclic ring system which can contain an additional oxygen or sulfur atom or an imino group which is unsubstituted or substituted by C.sub.1 -C.sub.3 alkyl.
摘要翻译：本发明涉及具有除草性能并且在不同作物栽培植物中具有良好选择性的新型1,3,4-噻二唑基氧基苯基脲。新颖的苯脲具有通式I其中X为氢，卤素或三氟甲基，Y为氢，可被氧中断或被卤素或氰基取代的C 1 -C 6烷基; C3-C6环烷基，环丙基甲基，未取代或被氯或C1-C4烷基取代的苯基; 或者是C1-C4烷硫基，C1-C4烷氧基，C1-C4烷基亚磺酰基或C1-C4烷基磺酰基，或氨磺酰基-SO2NR2R3，R1是氢或C1-C4烷基，R2是氢，可被中断的C1-C6烷基或被C 3 -C 6炔基或C 3 -C 6环烷基取代，或具有与R 2相同的含义或C 1 -C 6烷氧基，或者R 2和R 3与氮原子一起它们还可以形成可以含有另外的氧或硫原子的5或6元杂环体系或未被取代或被C 1 -C 3烷基取代的亚氨基。

3. 发明授权

US5077412A Substituted thioureas, isothioureas and carbodiimides 失效
标题翻译：取代的硫酸盐，同位素和碳水化合物
公开(公告)号：US5077412A
公开(公告)日：1991-12-31
申请号：US414998
申请日：1989-09-29
申请人： Josef Ehrenfreund , Manfred Boger , Odd Kristiansen , Jozef Drabek , Haukur Kristinsson
发明人： Josef Ehrenfreund , Manfred Boger , Odd Kristiansen , Jozef Drabek , Haukur Kristinsson
IPC分类号： A01N47/30 , A01N47/32 , A01N47/40 , A01N47/42 , C07D207/34 , C07D209/32 , C07D231/20 , C07D233/70 , C07D235/26 , C07D249/12 , C07D257/04 , C07D263/38 , C07D263/58 , C07D271/10 , C07D271/113 , C07D277/20 , C07D277/34 , C07D277/68 , C07D285/08 , C07D285/12 , C07D285/13 , C07D307/58 , C07D333/32 , C07D333/34
CPC分类号： C07D271/113 , A01N47/30 , A01N47/32 , A01N47/40 , A01N47/42 , C07D233/70 , C07D249/12 , C07D277/34 , C07D277/68 , C07D285/08 , C07D285/13
摘要： The invention relates to novel substituted phenylthioureas, phenylisothioureas and phenylcarbodiimides of formula I ##STR1## wherein Z is ##STR2## or --N.dbd.C.dbd.N--; R.sub.1 is C.sub.1 -C.sub.12 alkyl, C.sub.3 -C.sub.10 alkenyl, C.sub.3 -C.sub.10 alkynyl, C.sub.3 -C.sub.8 cycloalkyl, C.sub.1 -C.sub.3 alkyl substituted by 1 or 2 C.sub.3 -C.sub.6 cycloalkyl radicals, or is alkoxyalkyl containing a total of 3 to 10 carbon atoms, halogen-substituted C.sub.1 -C.sub.12 alkyl, polycyclic C.sub.7 -C.sub.10 cycloalkyl, or phenyl(C.sub.1 -C.sub.5)alkyl which may be substituted in the phenyl moiety by 1 or 2 identical or different members selected from the group consisting of halogen, methoxy, ethoxy and C.sub.1 -C.sub.5 alkyl,R.sub.2 is hydrogen or C.sub.1 -C.sub.5 alkyl,R.sub.3 is C.sub.1 -C.sub.5 alkyl or C.sub.3 -C.sub.6 cycloalkyl,R.sub.4 is hydrogen or C.sub.1 -C.sub.4 alkyl,R.sub.5 is a 5-membered heterocyclic radical containing 1 to 4 hetero atoms selected from the group consisting of N, O and S, which radical may be substituted at the carbon or nitrogen atoms by 1 to 3 of the substituents R.sub.6, R.sub.7 and R.sub.8, or is a 5-membered heterocyclic radical which may be fused with benzene nuclei and which contains 1 or 2 hetero atoms selected from the group consisting of N, O and S and can be substituted at the carbon or nitrogen atoms by 1 to 3 of the substituents R.sub.6, R.sub.7 and R.sub.8,R.sub.6 and R.sub.7 are each independently of the other hydrogen, halogen, C.sub.1 -C.sub.4 alkyl, halogen-substituted C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy; halogen-substituted C.sub.1 -C.sub.4 alkoxy, phenyl, or C.sub.1 -C.sub.4 alkylthio,R.sub.8 is hydrogen or C.sub.1 -C.sub.4 alkyl, andR.sub.9 is C.sub.1 -C.sub.5 alkyl, C.sub.2 -C.sub.5 alkenyl, C.sub.3 -C.sub.4 alkynyl, alkoxyalkyl containing a total of 10 carbon atoms, or alkylthioalkyl containing a total of 10 carbon atomsand to the salts thereof with acids and bases. The invention further relates to the preparation of these compounds and to the use thereof in pest control, and to novel intermediates.

4. 发明授权

US4629802A Sulfonyl carbonoimidates 失效
标题翻译：磺酰基碳酰亚胺酯
公开(公告)号：US4629802A
公开(公告)日：1986-12-16
申请号：US707358
申请日：1985-03-01
申请人： Haukur Kristinsson , Werner Topfl
发明人： Haukur Kristinsson , Werner Topfl
IPC分类号： C07D251/46 , A01N47/36 , A01N47/42 , C07C67/00 , C07C301/00 , C07C303/38 , C07C303/40 , C07C311/63 , C07D239/42 , C07D239/47 , C07D251/16 , C07D521/00 , C07C119/20
CPC分类号： C07D521/00
摘要： A novel process for producing sulfonylureas of the formula I having a herbicidal action and an action regulating plant growth ##STR1## wherein A is an unsubstituted or substituted phenyl, naphthyl, furan, thiophene or pyridine group, E is a nitrogen atom or the methine group, R.sub.a is hydrogen, halogen, C.sub.1 -C.sub.5 -alkyl, C.sub.1 -C.sub.5 -haloalkyl, C.sub.1 -C.sub.5 -alkoxy, C.sub.1 -C.sub.5 -haloalkoxy, C.sub.1 -C.sub.5 -alkylthio or C.sub.2 -C.sub.10 -alkoxyalkoxy, and R.sub.b is the same as R.sub.a or is an unsubstituted or substituted amino group, and salts thereof, which process comprises firstly condensing an imidocarbonic acid ester with a sulfonyl chloride of the formula II to the sulfonylimidocarbonic acid diester of the formula IV ##STR2## wherein R is an alkyl group, and reacting this in an ethereal solvent in the presence of sodium hydride or potassium tertbutylate with a 2-aminopyrimidine or 2-amino-1,3,5-triazine of the formula V, and finally reacting the formed sulfonylisourea of the formula VI in an organic solvent with hydrochloric acid to obtain the sulfonylurea of the formula I, and isolating this as such or as a salt; ##STR3## The sulfonylimidocarbonic acid diesters of the formula IV and certain sulfonylisoureas of the formula VI, required as intermediates, are novel compounds. The process has the advantage that no sulfonamides are needed as intermediates.
摘要翻译：一种制备具有除草作用和调节植物生长作用的式I的磺酰脲的新方法，其中A是未取代或取代的苯基，萘基，呋喃，噻吩或吡啶基，E是氮原子或次甲基，R a为氢，卤素，C 1 -C 5 - 烷基，C 1 -C 5 - 卤代烷基，C 1 -C 5 - 烷氧基，C 1 -C 5 - 卤代烷氧基，C 1 -C 5 - 烷硫基或C 2 -C 10 - 烷氧基烷氧基，Rb为与R a相同或为未取代或取代的氨基及其盐，该方法包括首先将亚氨基碳酸酯与式II的磺酰氯缩合成式IV的磺酰亚胺基碳酸二酯其中R是烷基并将其在惰性溶剂中，在氢化钠或叔丁醇钾存在下与式V的2-氨基嘧啶或2-氨基-1,3,5-三嗪反应，最后使形成的式VI的磺酰基异脲在有盐酸的有机溶剂中在式I的磺酰脲中，并将其分离为盐或盐; 作为中间体，式IV的磺酰亚胺基碳酸二酯和式VI的某些磺酰基异脲是新化合物。该方法的优点是不需要磺酰胺作为中间体。

5. 发明授权

US5783704A Pyridine derivatives as pesticides 失效
标题翻译：吡啶衍生物作为农药
公开(公告)号：US5783704A
公开(公告)日：1998-07-21
申请号：US669452
申请日：1996-06-28
申请人： Henry Szczepanski , Haukur Kristinsson , Peter Maienfisch , Josef Ehrenfreund
发明人： Henry Szczepanski , Haukur Kristinsson , Peter Maienfisch , Josef Ehrenfreund
IPC分类号： A01C20060101 , A01N20060101 , A01N43/40 , A01N43/50 , A01N43/54 , A01N43/653 , A01N43/707 , A01N43/76 , A01N43/78 , A01N43/824 , A01N43/88 , C07D20060101 , C07D253/06 , C07D285/12 , C07D285/13 , C07D401/12 , C07D413/12 , C07D417/12
CPC分类号： C07D253/06 , A01N43/40 , A01N43/50 , A01N43/653 , C07D285/13 , C07D401/12
摘要： Compounds of formu (I) wherein n and Z are as defined in claim 1, and, where appropriate, tautomers thereof, in each case in free form, or in salt form, can be used as agrochemical active ingredients and can be prepared in a manner known per se.
摘要翻译： PCT No.PCT / EP94 / 04222 Sec。 371日期：1996年6月28日 102（e）日期1996年6月28日PCT 1994年12月19日PCT公布。 WO95 / 18123 PCT出版物日期1995年7月6日，其中n和Z如权利要求1中所定义的formu（I）化合物，并且在适当的情况下，其互变异构体以游离形式或盐形式，可用作农业化学活性成分，可以以本身已知的方式制备。

6. 发明授权

US5561230A Process for the preparation of aminotriazine derivatives 失效
标题翻译：氨基三嗪衍生物的制备方法
公开(公告)号：US5561230A
公开(公告)日：1996-10-01
申请号：US460342
申请日：1995-06-02
申请人： Ernst Beriger , Haukur Kristinsson
发明人： Ernst Beriger , Haukur Kristinsson
IPC分类号： C07D253/06 , C07D271/10 , C07D271/113 , C07D401/12 , C07D413/06
CPC分类号： C07D253/06 , C07D271/113 , C07D401/12 , C07D413/06
摘要： The invention relates to a process for the preparation of a compound of formula ##STR1## useful as intermediate for the preparation of pesticides, wherein R is hydrogen, C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, C.sub.1 -C.sub.4 alkyl substituted by from 1 to 10 halogen atoms or by from 1 to 3 radicals selected from the group consisting of C.sub.1 -C.sub.3 alkoxy, C.sub.1 -C.sub.3 alkylthio and phenyl, phenyl or phenyl substituted by from 1 to 3 radicals selected from the group consisting of halogen, methyl, ethyl, methoxy, methylthio and nitro, which comprises reacting with hydrazine hydrate a compound of formula ##STR2## wherein R.sub.1 is hydrogen, C.sub.1 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl, C.sub.1 -C.sub.4 alkyl substituted by from 1 to 9 chlorine atoms, C.sub.1 -C.sub.3 alkoxy, C.sub.1 -C.sub.3 alkylthio, C.sub.1 -C.sub.3 alkylsulfinyl, C.sub.1 -C.sub.3 alkylsulfonyl, phenyl, phenyl substituted by from 1 to 3 radicals selected from the group consisting of halogen, methyl, ethyl, methoxy, methylthio and nitro, or pyridyl, and subjecting to hydrolysis the resulting compound of formula ##STR3##
摘要翻译：本发明涉及制备式（I）化合物的方法，其可用作制备农药的中间体，其中R是氢，C 1 -C 6烷基，C 3 -C 6环烷基，被1至 10个卤素原子或1至3个选自C 1 -C 3烷氧基，C 1 -C 3烷硫基和苯基的基团，苯基或被1至3个选自卤素，甲基，乙基，甲氧基，甲硫基和硝基，其包括与水合肼反应其中R 1是氢，C 1 -C 4烷基，C 3 -C 6环烷基，被1至9个氯原子取代的C 1 -C 4烷基，C 1 -C 3烷氧基，C 1 C 3烷硫基，C 1 -C 3烷基亚磺酰基，C 1 -C 3烷基磺酰基，苯基，被1至3个选自卤素，甲基，乙基，甲氧基，甲硫基和硝基或吡啶基的基取代的苯基，并将所得化合物公式（III）

7. 发明授权

US4388464A Thiadiazolyl-glyoxylonitrile-2-oxime ether derivatives for protecting plant crops 失效
标题翻译：噻二唑基 - 乙醛腈-2-肟醚衍生物，用于保护植物作物
公开(公告)号：US4388464A
公开(公告)日：1983-06-14
申请号：US232752
申请日：1981-02-09
申请人： Haukur Kristinsson , Beat Muller , Johannes P. Pachlatko
发明人： Haukur Kristinsson , Beat Muller , Johannes P. Pachlatko
IPC分类号： A01N25/32 , A01N43/824 , C07C251/32 , C07C259/10 , C07C311/16 , C07C317/32 , C07C317/44 , C07C317/46 , C07C317/48 , C07C323/47 , C07C327/20 , C07D213/53 , C07D213/61 , C07D213/64 , C07D213/65 , C07D213/69 , C07D213/70 , C07D213/79 , C07D215/32 , C07D215/34 , C07D233/26 , C07D233/86 , C07D235/14 , C07D235/16 , C07D249/06 , C07D263/56 , C07D263/58 , C07D277/64 , C07D285/12 , C07D285/125 , C07D285/13 , C07D307/20 , C07D307/52 , C07D309/20 , C07D309/32 , C07D311/58 , C07D317/58 , C07D335/06 , C07D339/06 , C07D339/08 , A01N43/82 , A01N47/40
CPC分类号： C07D213/53 , C07D213/61 , C07D213/64 , C07D213/65 , C07D213/69 , C07D213/70 , C07D213/79 , C07D215/32 , C07D215/34 , C07D233/26 , C07D233/86 , C07D235/14 , C07D235/16 , C07D249/06 , C07D263/56 , C07D277/64 , C07D285/12 , C07D285/125 , C07D285/13 , C07D307/20 , C07D307/52 , C07D309/20 , C07D309/32 , C07D311/58 , C07D317/58 , C07D335/06 , C07D339/06 , C07D339/08 , Y10S47/03
摘要： A process for protecting cultivated plants against aggressive agricultural chemicals is described in which oxime derivatives of the formula ##STR1## are used as antidotes. Either the cultivated area for the cultivated plants or the cultivated plants themselves or parts of the plant (seeds, tubers, stem parts and the like), as desired, can be treated with these oxime derivatives, which are used as a dressing.Ar is a phenyl radical of the formula ##STR2## or Ar is also a 5-membered to 10-membered heterocyclic radical which contains not more than three identical or different hetero-atoms N, O and/or S and which can be bonded via a C.sub.1 - to C.sub.3 -aliphatic chain to the remainder of the molecule and which is substituted by R.sub.1, R.sub.2 or R.sub.3 and can be substituted by oxo or thiono; X is hydrogen, CN, halogen, C.sub.1 -C.sub.10 -alkyl, lower alkanoyl, --COOH, a carboxylic acid ester of a carboxamide radical; and Q is hydrogen, lower alkyl, which can be interrupted by hetero-atoms or substituted by halogen or cyano, lower alkenyl or halogenoalkenyl, lower alkynyl, C.sub.3 -C.sub.7 cycloalkyl, which is unsubstituted or substituted by halogen, or a lower alkanecarboxylic acid ester group, a lower alkanecarboxylic acid thioester group, a lower alkanecarboxamide group, an aliphatic acyl radical, an araliphatic, cycloaliphatic or substituted or unsubstituted aromatic or heterocyclic acyl radical, an alkylsulfonyl radical, a sulfonamide radical, a metal salt, a quaternized ammonium salt or an aliphatic, araliphatic, cycloaliphatic or substituted or unsubstituted aromatic or heterocyclic carbonic acid, thiocarbonic acid or carbamoyl radical.
摘要翻译：描述了用于保护栽培植物免受侵袭性农药的方法，其中使用式“IMAGE”的肟衍生物作为解毒剂。根据需要，可以用这些用作敷料的肟衍生物来处理栽培植物或栽培植物本身或植物的部分（种子，块茎，茎部等）的栽培面积。 Ar是下式的苯基或Ar也是5元至10元杂环基，其含有不超过三个相同或不同的杂原子N，O和/或S，并且可以通过与分子的其余部分存在的C 1 -C 3 - 脂族链，并被R 1，R 2或R 3取代并且可被氧代或硫代替代; X是氢，CN，卤素，C 1 -C 10 - 烷基，低级烷酰基，-COOH，羧酰胺基的羧酸酯; Q为氢原子，可被杂原子或被卤素或氰基取代的低级烷基，低级链烯基或卤代烯基，低级炔基，未被取代或被卤素取代的C3-C7环烷基或低级链烷羧酸酯低级链烷羧酸硫酯基，低级链烷酰胺基，脂族酰基，芳脂族，脂环族或取代或未取代的芳族或杂环酰基，烷基磺酰基，磺酰胺基，金属盐，季铵化铵盐或脂族，芳脂族，脂环族或取代或未取代的芳族或杂环碳酸，硫代碳酸或氨基甲酰基。

8. 发明授权

US4254133A Combatting ectoparasites with phenylaminoalkyl-2-imidazoline compounds 失效
标题翻译：将外寄生虫与苯基氨基烷基-2-咪唑啉化合物作用
公开(公告)号：US4254133A
公开(公告)日：1981-03-03
申请号：US42822
申请日：1979-05-29
申请人： Haukur Kristinsson , Walter Traber
发明人： Haukur Kristinsson , Walter Traber
IPC分类号： A01N43/50 , C07D233/24
CPC分类号： C07D233/24
摘要： Compositions containing active substances of the formula ##STR1## wherein R.sub.1 and R.sub.2, each independently of the other, represent hydrogen or alkyl of 1 to 10 carbon atoms, R.sub.3 and R.sub.4, each independently of the other, represent alkyl of 1 to 5 carbon atoms or halogen, preferably chlorine, and R.sub.5 represents hydrogen, alkyl of 1 to 5 carbon atoms or halogen, or an acid addition salt thereof for combating ectoparasites.
摘要翻译：包含式IMA活性物质的组合物，其中R 1和R 2各自独立地表示氢或1至10个碳原子的烷基，R 3和R 4各自独立地表示1至5个碳原子的烷基或卤素，优选氯，R5表示氢，1〜5个碳原子的烷基或卤素，或其酸加成盐，用于对抗外寄生物。

9. 发明授权

US6034083A Pyridine derivatives as pesticides 失效
标题翻译：吡啶衍生物作为农药
公开(公告)号：US6034083A
公开(公告)日：2000-03-07
申请号：US119285
申请日：1998-07-20
申请人： Henry Szczepanski , Haukur Kristinsson , Peter Maienfisch , Josef Ehrenfreund
发明人： Henry Szczepanski , Haukur Kristinsson , Peter Maienfisch , Josef Ehrenfreund
IPC分类号： A01C20060101 , A01N20060101 , A01N43/40 , A01N43/50 , A01N43/54 , A01N43/653 , A01N43/707 , A01N43/76 , A01N43/78 , A01N43/824 , A01N43/88 , C07D20060101 , C07D253/06 , C07D285/12 , C07D285/13 , C07D401/12 , C07D413/12 , C07D417/12 , A61K31/53
CPC分类号： C07D253/06 , A01N43/40 , A01N43/50 , A01N43/653 , C07D285/13 , C07D401/12
摘要： Compounds of formula ##STR1## wherein n and Z are as defined in claim 1, and, where appropriate, tautomers thereof, in each case in free form or in salt form, can be used as agrochemical active ingredients and can be prepared in a manner known per se.
摘要翻译：其中n和Z如权利要求1所定义的化合物，并且在适当的情况下，其互变异构体在每种情况下以游离形式或盐形式可用作农业化学活性成分，并且可以以本身已知的方式制备。

10. 发明授权

US5679623A Imidazole derivatives 失效
标题翻译：咪唑衍生物
公开(公告)号：US5679623A
公开(公告)日：1997-10-21
申请号：US460473
申请日：1995-06-02
申请人： Henry Szczepanski , Haukur Kristinsson
发明人： Henry Szczepanski , Haukur Kristinsson
IPC分类号： A01N43/50 , A01N47/16 , A01N47/38 , C07D233/70 , C07D233/88 , C07D401/12 , C07D403/12 , C07D413/12 , C07D417/12 , C07D213/36 , C07D233/36
CPC分类号： C07D401/12 , A01N43/50 , A01N47/16 , A01N47/38 , C07D233/70
摘要： Compounds of the formula ##STR1## in which R.sub.l, R.sub.2, R.sub.3, R.sub.4, Y and Z are as defined in claim 1, and, if appropriate, the tautomers thereof, in each case in free form or in salt form, can be used as agrochemical active ingredients and can be prepared in a manner known per se.
摘要翻译：其中R 1，R 2，R 3，R 4，Y和Z如权利要求1中所定义的式（Ⅰ）化合物，如果合适，其互变异构体在每种情况下为游离形式或盐形式，可以用作农药活性成分，并且可以以本身已知的方式制备。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式