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41. 发明授权

US5166392A Fungicidal derivatives of carbocyclic anilides 失效
标题翻译：杀虫剂的杀真菌剂
公开(公告)号：US5166392A
公开(公告)日：1992-11-24
申请号：US568454
申请日：1990-08-15
申请人： Bernd-Wieland Kruger , Klaus Sasse , Wilhelm Brandes
发明人： Bernd-Wieland Kruger , Klaus Sasse , Wilhelm Brandes
IPC分类号： A01N37/18 , A01N37/24 , A01N47/06 , A01N53/00 , A01N53/12 , C07C231/02 , C07C231/14 , C07C233/60
CPC分类号： A01N47/06 , A01N37/24 , A01N53/00 , C07C233/60 , C07C2101/14 , C07C2101/16
摘要： Fungicidal derivatives of carboxyclic anilides of the formula ##STR1## in which X represent optionally alkyl-substituted cycloalkyl or optionally alkyl-substituted cycloalkenyl,Hal represents halogen, andY.sup.1, Y.sup.2 and Y.sup.3 independently of one another represent hydrogen, halogen, optionally halogen-substituted alkyl, optionally halogen-substituted alkoxy or optionally halogen-substituted alkylthio, andZ represents the groups COOR.sup.2 or COR.sup.1, whereR.sup.1 and R.sup.2 are identical or different and represent optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl, polyalkoxyalkyl and optionally substituted cycloalkyl, optionally substituted phenyl, optionally substituted phenylalkyl or substituted phenoxyalkyl.
摘要翻译：式（I）的羧基苯胺的杀真菌衍生物，其中X表示任选烷基取代的环烷基或任选的烷基取代的环烯基，Hal表示卤素，并且Y 1，Y 2和Y 3彼此独立地表示氢，卤素，任选地卤素取代的烷基，任选卤素取代的烷氧基或任选的卤素取代的烷硫基，Z代表基团COOR 2或COR 1，其中R 1和R 2相同或不同，并且代表任选卤素取代的烷基，烯基，烷氧基烷基，烷硫基烷基，聚烷氧基烷基和任选取代的环烷基，任选取代的苯基，任选取代的苯基烷基或取代的苯氧基烷基。

42. 发明授权

US5008261A Agents for repelling insects and mites 失效
标题翻译：用于排斥昆虫和螨虫的药剂
公开(公告)号：US5008261A
公开(公告)日：1991-04-16
申请号：US423070
申请日：1989-10-18
申请人： Bernd-Wieland Kruger , Klaus Sasse , Franz-Peter Hoever , Gunther Nentwig , Wolfgang Behrenz
发明人： Bernd-Wieland Kruger , Klaus Sasse , Franz-Peter Hoever , Gunther Nentwig , Wolfgang Behrenz
IPC分类号： A01N20060101 , A01N47/10 , A01N47/12 , A01N47/16 , A01N47/18 , C07C20060101 , C07C67/00 , C07C239/00 , C07C269/04 , C07C269/06 , C07C271/12 , C07C271/16 , C07D20060101 , C07D211/22 , C07D227/04
CPC分类号： C07C271/16 , A01N47/12 , A01N47/16 , A01N47/18 , C07D211/22 , C07C2101/02 , C07C2101/14 , Y10S514/919
摘要： It has been found that the substituted .alpha.,.omega.-amino-alcohol derivatives, some of which are known, of the formula I ##STR1## in which X represents hydrogen, COR.sup.11, COOR.sup.12 or R.sup.13,R.sup.1 represents optionally substituted alkyl, alkenyl or alkinyl radicalsR.sup.2, R.sup.11, R.sup.12 and R.sup.13 are identical or different and represent optionally substituted alkyl or alkenyl radicals,R.sup.3 to R.sup.10 are identical or different and represent hydrogen, or represent optionally substituted alkyl radicals,and whereinR.sup.2 and R.sup.3 or R.sup.3 and R.sup.7 or R.sup.3 and R.sup.5 or R.sup.5 and R.sup.7, together with the atoms to which they are bonded, can also form an optionally substituted monocyclic ring, andn and m are identical or different and denote 0 or 1,with the proviso that X does not represent hydrogen or R.sup.13 if n and m represent 0,have a powerful insect- and mite-repelling action (repellent action).

43. 发明授权

US4772608A 1-heteroaryl-4-aryl-pyrazole microbicides 失效
标题翻译： 1-杂芳基-4-芳基 - 吡唑杀微生物剂
公开(公告)号：US4772608A
公开(公告)日：1988-09-20
申请号：US886284
申请日：1986-07-15
申请人： Klaus Sasse , Gerd Hanssler , Hans-Georg Schmitt , Wilfried Paulus
发明人： Klaus Sasse , Gerd Hanssler , Hans-Georg Schmitt , Wilfried Paulus
IPC分类号： A01N43/40 , A01N43/56 , A01N47/06 , A01N47/16 , A01N47/22 , C07D401/04 , C07D403/04 , C07D405/14 , A61K31/505
CPC分类号： C07D401/04 , A01N43/56 , A01N47/06 , A01N47/16 , A01N47/22 , C07D403/04 , C07D405/14
摘要： Novel microbicidally active 1-heteroaryl-4-aryl-pyrazole derivatives of the formulae (I) and/or (1A) ##STR1## in which R represents hydrogen or alkyl,R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, a radical--S(O).sub.p -alkyl which is optionally substituted in the alkyl part, nitro or optionally substituted amino, or represents a fused-on carbocyclic or heterocyclic radicalp represents the integer 0, 1 or 2,n represents an integer from 0 to 5,X represents .dbd.CH--, or represents a nitrogen atom,Y represents CO or SO.sub.2 andR.sup.2 represents hydrogen, in each case optionally substituted alkyl, cycloalkyl or aryl or a heterocyclic radical, or represents OR.sup.3, or also represents SR.sup.3, if Y is CO,whereinR.sup.3 represents optionally substituted alkyl or aryl, orR.sup.2 represents a radical ##STR2## wherein R.sup.4 represents hydrogen or saturated or unsaturated optionally substituted alkyl andR.sup.5 represents hydrogen, saturated or unsaturated, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl or an optionally substituted heterocyclic radical, orR.sup.4 and R.sup.5, together with the nitrogen atom on which they are located, form a heterocyclic ring which optionally contains further hetero atoms and can optionally be mono- or polysubstituted by identical or different substituents.
摘要翻译：式（I）和/或（1A）的新型杀微生物活性1-杂芳基-4-芳基 - 吡唑衍生物其中R表示氢或烷基，R1表示卤素，羟基，任选取代的烷基，任选取代的烷氧基，在烷基部分任选取代的基团-S（O）对 - 烷基，硝基或任选取代的氨基，或表示稠合的碳环或杂环基p表示整数0， 1或2，n表示0〜5的整数，X表示= CH-，或表示氮原子，Y表示CO或SO2，R2表示氢，在各情况下为任意取代的烷基，环烷基或芳基或杂环基，或表示OR 3，或者也表示SR 3，如果Y是CO，其中R 3表示任选取代的烷基或芳基，或R 2表示基团，其中R 4表示氢或饱和或不饱和的任选取代的烷基，R 5表示氢，饱和或不饱和的，可选地取代的烷基，任选取代的环烷基，任选取代的芳基或任选取代的杂环基，或R 4和R 5与它们所位于的氮原子一起形成任选含有其它杂原子的杂环，并且可以任选地是单或被相同或不同取代基多取代。

44. 发明授权

US4145439A Combating pests with benzyl phenyl ethers 失效
标题翻译：与BENZYL PHENYL ETHERS组合生产
公开(公告)号：US4145439A
公开(公告)日：1979-03-20
申请号：US809492
申请日：1977-06-23
申请人： Andreas Schulze , Klaus Sasse , Klaus Naumann , Peter Roessler , Peter Kraus
发明人： Andreas Schulze , Klaus Sasse , Klaus Naumann , Peter Roessler , Peter Kraus
IPC分类号： A01N33/10 , A01N35/08 , C07D307/52 , A01N9/28 , A01N9/20 , C07C93/06 , C07D307/14
CPC分类号： C07D307/52
摘要： Benzyl phenyl ethers, many of which are new, of the formula ##STR1## in which X is ##STR2## R.sup.1 is H or alkyl, R.sup.2 is alkyl, alkenyl, alkynyl, alkylidene, alkenylidene or alkynylidene optionally substituted by OH, alkoxy, a heterocyclic group containing O, S or N, amino, monoalkylamino, dialkylamino or by an alkylene bridge with 5 carbon atoms, R.sup.3 each independently is H, alkyl, alkoxy, alkylmercapto, halogen, halogenoalkyl, halogenoalkoxy, halogenoalkylmercapto, NO.sub.2, amino, monoalkylamino or dialkylamino, R.sup.4 each independently is H, halogen or alkoxy, M is an integer from 1 to 5, and N is an integer from 1 to 4, And acid addition salts thereof, are useful for combatting arthropods, nematodes, fungi and bacteria.
摘要翻译：其中许多是新的式（I）其中X是R 1是H或烷基，R 2是任选被OH取代的烷基，烯基，炔基，亚烷基，亚烯基或亚炔基，烷氧基，含有O，S或N的杂环基，氨基，单烷基氨基，二烷基氨基或具有5个碳原子的亚烷基桥，R3各自独立地为H，烷基，烷氧基，烷基巯基，卤素，卤代烷基，卤代烷氧基，卤代烷基巯基，NO2，氨基，单烷基氨基或二烷基氨基，R4各自独立地为H，卤素或烷氧基，m为1至5的整数，n为1至4的整数，及其酸加成盐可用于与节肢动物，线虫，真菌和/ 菌。

45. 发明授权

US3963749A 1-Methyl-2,3-dihydro-1,4-dithiinium methosulfate 失效
标题翻译： 1-甲基-2,3-二氢-1,4-二硫鎓甲硫酸盐
公开(公告)号：US3963749A
公开(公告)日：1976-06-15
申请号：US476765
申请日：1974-06-05
申请人： Klaus Naumann , Klaus Lurssen , Klaus Sasse
发明人： Klaus Naumann , Klaus Lurssen , Klaus Sasse
IPC分类号： A01N43/32 , C07D339/08
CPC分类号： C07D339/08
摘要： 1,4-DITHIENE SULFONIUM SALTS OF THE FORMULA ##SPC1##In whichR is alkyl, substituted alkyl, alkenyl, alkynyl of up to 8 carbon atoms; cycloalkyl, aralkyl; or aralkyl substituted in the aryl moiety;Z is hydrogen or alkyl, andA.sup.- is one equivalent of an anionAre outstandingly effective as plant growth regulants, e.g., as plant growth inhibitors.
摘要翻译：其中R是烷基，取代的烷基，烯基，至多8个碳原子的炔基; 环烷基，芳烷基; 或在芳基部分取代的芳烷基; Z是氢或烷基，并且A 1是1当量的阴离子作为植物生长调节剂E.E.As植物生长抑制剂的有效效果。

46. 发明授权

US5703103A Thiazolylpyrazolinones and their use for protecting technical materials 失效
标题翻译：噻唑吡唑啉酮及其用于保护技术材料的用途
公开(公告)号：US5703103A
公开(公告)日：1997-12-30
申请号：US716239
申请日：1996-09-24
申请人： Lutz Heuer , Peter Wachtler , Martin Kugler , Heinrich Schrage , Klaus Sasse
发明人： Lutz Heuer , Peter Wachtler , Martin Kugler , Heinrich Schrage , Klaus Sasse
IPC分类号： C07D231/20 , A01N43/78 , A61K31/42 , A61P31/00 , C07D417/04 , C07D417/14 , C08K5/47 , C09D5/14 , D06M16/00 , D21H21/36
CPC分类号： C07D417/04 , A01N43/78 , C07D417/14 , C08K5/47 , C09D5/14 , D06M16/00 , D21H21/36
摘要： The present invention relates to novel thiazolylpyrazolinones, a process for their preparation and their use for the protection of technical materials.
摘要翻译： PCT No.PCT / EP95 / 01032 Sec。 371日期：1996年9月24日 102（e）1996年9月24日PCT 1995年3月20日PCT PCT。第WO95 / 26962号公报日期1995年10月12日本发明涉及新型噻唑吡唑啉酮，其制备方法及其用于保护技术材料的用途。

47. 发明授权

US4698344A 1-Heteroaryl-4-aryl-pyrazolin-5-ones for use as medicaments 失效
标题翻译： 1-杂芳基-4-芳基 - 吡唑啉-5-酮，用作药物
公开(公告)号：US4698344A
公开(公告)日：1987-10-06
申请号：US800485
申请日：1985-11-21
申请人： Klaus Sasse , Michael Hammond , Friedel Seuter , Elisabeth Perzborn , Bernhard Pelster , Graham Sturton , Trevor Abram
发明人： Klaus Sasse , Michael Hammond , Friedel Seuter , Elisabeth Perzborn , Bernhard Pelster , Graham Sturton , Trevor Abram
IPC分类号： C07D213/77 , A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4412 , A61K31/4418 , A61K31/4427 , A61K31/443 , A61K31/505 , A61P7/02 , A61P29/00 , A61P37/08 , C07D231/22 , C07D251/46 , C07D317/00 , C07D401/04 , C07D403/04 , C07D405/14 , C12N9/99
CPC分类号： C07D401/04 , C07D403/04 , C07D405/14
摘要： The invention relates to 1-heteroaryl-4-aryl-pyrazolin-5-ones, a preparation process and the use in combating diseases, in particular for use as lipoxygenase inhibitors.
摘要翻译：本发明涉及1-杂芳基-4-芳基 - 吡唑啉-5-酮，其制备方法以及抗疾病特别用作脂氧合酶抑制剂的用途。

48. 发明授权

US4663365A Wash-resistant, antimicrobially-active fibres and threads and their manufacture 失效
标题翻译：耐洗涤，抗微生物活性纤维和线及其制造
公开(公告)号：US4663365A
公开(公告)日：1987-05-05
申请号：US762652
申请日：1985-08-05
申请人： Ulrich Reinehr , Klaus Sasse , Gerhard Jager , Walter Radt
发明人： Ulrich Reinehr , Klaus Sasse , Gerhard Jager , Walter Radt
IPC分类号： C08L33/00 , A01N43/50 , A01N43/54 , C08K5/00 , C08K5/34 , C08K5/3442 , C08K5/3445 , C08K5/3462 , C08L33/02 , C08L33/18 , C08L33/20 , D01F1/10 , D01F6/54 , D06M23/00 , D06M101/00 , D06M101/16 , D06M101/30
CPC分类号： C08K5/3445 , A01N43/50 , A01N43/54 , C08K5/3462 , D01F1/103
摘要： Threads and fibres of synthetic polymers containing from 0.1 to 5% by weight, based on the polymer, of one or more than one compound corresponding to the formula (I) ##STR1## wherein R represents hydrogen or alkyl,R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted phenoxy, a group --S(O).sub.p -alkyl which is optionally substituted in the alkyl portion, nitro, optionally substituted amino or a condensed carbocyclic or heterocyclic group,p stands for the numerical value 0, 1 or 2,R.sup.2 represents halogen, alkyl which is optionally substituted, alkoxy, alkylmercapto, nitro, cyano, carboxylic acid amide or a condensed carbocyclic group,m represents an integer from 0 to 5,n represents an integer from 0 to 4, the substituents being either identical or different when m and/or n has a value greater than 1, and X, Y and Z are identical or different and represent a nitrogen atom, the group .dbd.CH-- or ##STR2## where R.sup.2 has the meaning indicated above, with the proviso that at least one of the substituents, X, Y and Z is a nitrogen atom,manifest antimicrobial activity which persists even after dyeing and washing processes.
摘要翻译：含有0.1至5重量％的合成聚合物的线和纤维，基于聚合物，对应于式（I）的一种或多种化合物其中R表示氢或烷基，R 1表示卤素，羟基，任选取代的烷基，任选取代的烷氧基，任选取代的苯氧基，在烷基部分任选取代的-S（O）对 - 烷基，硝基，任选取代的氨基或稠合的碳环或杂环基，p代表数值0,1或2，R2表示卤素，任选取代的烷基，烷氧基，烷基巯基，硝基，氰基，羧酸酰胺或稠合碳环基团，m表示0至5的整数，n表示 0至4时，当m和/或n具有大于1的值时，取代基相同或不同，X，Y和Z相同或不同，表示氮原子，基团= CH-或其中 R2有意义我附带说明的是，X，Y和Z中的至少一个取代基是氮原子，表现出即使在染色和洗涤过程之后仍然存在的抗微生物活性。

49. 发明授权

US4663327A 1-heteroaryl-4-aryl-pyrazolin-5-ones 失效
标题翻译： 1-杂芳基-4-芳基 - 吡唑啉-5-酮
公开(公告)号：US4663327A
公开(公告)日：1987-05-05
申请号：US733450
申请日：1985-05-10
申请人： Klaus Sasse , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke , Hans-Georg Schmitt , Wilfried Paulus
发明人： Klaus Sasse , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke , Hans-Georg Schmitt , Wilfried Paulus
IPC分类号： C07D251/46 , A01N43/40 , A01N43/42 , A01N43/54 , A01N43/56 , A01N43/66 , A01N47/02 , C07D213/77 , C07D215/38 , C07D215/42 , C07D217/22 , C07D239/42 , C07D239/47 , C07D251/16 , C07D251/22 , C07D317/00 , C07D401/04 , C07D401/12 , C07D403/04 , C07D405/14 , A61K31/53 , A61K31/44 , A61K31/505
CPC分类号： C07D401/04 , A01N43/56 , A01N43/66 , A01N47/02 , C07D403/04
摘要： Microbicidally active novel 1-heteroaryl-4-aryl-pyrazolin-5-ones of the formula ##STR1## in which R represents hydrogen or alkyl,R.sup.1 represents halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted phenoxy, a radical --S(O).sub.p -- alkyl which is optionally substituted in the alkyl part, nitro, optionally substituted amino or a fused-on carbocyclic or heterocyclic radical,p represents an integer 0, 1 or 2,R.sup.2 represents halogen or optionally substituted alkyl, or represents alkoxy, alkylmercapto, nitro, cyano, carboxamide or a fused-on carbocyclic radical,m represents an integer from 0 to 5,n represents an integer from 0 to 4, it being possible for the substituents to be identical or different when m and/or n represent a number greater than 1, andX, Y and Z are identical or different and represent a nitrogen atom or the radical .dbd.CH or ##STR2## wherein R.sup.2 has the meaning given above, with the proviso that at least one of the radicals X, Y and Z denotes a nitrogen atom.
摘要翻译：具有式“IMAGE”的杀微生物活性的新颖的1-杂芳基-4-芳基 - 吡唑啉-5-酮，其中R表示氢或烷基，R1表示卤素，羟基，任选取代的烷基，任选取代的烷氧基，任选取代的苯氧基，在烷基部分任选取代的-S（O）p-烷基，硝基，任选取代的氨基或稠合的碳环或杂环基，p表示整数0,1或2，R 2表示卤素或任选取代的烷基，或表示烷氧基，烷基巯基，硝基，氰基，甲酰胺或稠合的碳环基团，m表示0至5的整数，n表示0至4的整数，当m取代时，取代基可以相同或不同和/或n表示大于1的数，X，Y和Z相同或不同，表示氮原子或基团= CH或，其中R2具有上述含义，条件是至少一个的基团X，Y和 Z表示氮原子。

50. 发明授权

US4027037A N-substituted .beta.-aminocrotonic acid esters 失效
公开(公告)号：US4027037A
公开(公告)日：1977-05-31
申请号：US557698
申请日：1975-03-12
申请人： Peter Siegle , Klaus Sasse , Peter Rossler
发明人： Peter Siegle , Klaus Sasse , Peter Rossler
IPC分类号： A01N37/44 , A01N43/46 , C07C67/00 , C07C227/08 , C07C229/30 , C07C313/00 , C07C323/17 , C07C323/25 , C07C323/30 , C07D223/04 , C07D295/145 , C07C101/28 , A01N9/20
CPC分类号： C07D295/145 , A01N37/44
摘要： N-substituted .beta.-aminocrotonic acid esters of the formula ##STR1## in which R.sup.1 is hydrogen, or alkyl or alkenyl with up to 4 carbon atoms;R.sup.2 is straight-chain or branched alkyl or alkenyl with up to 9 carbon atoms, optionally interrupted by O or S, and optionally substituted by halogen, phenoxy, dimethylamino, cyclic alkyl or alkenyl with up to 8 carbon atoms which are optionally substituted by halogen, dimethylamino, or alkyl, alkoxy or alkylthio with up to 4 carbon atoms, phenyl which is optionally substituted by halogen, dimethylamino, phenoxy, or alkyl, alkenyl, acyl, alkoxy, alkenoxy or alkynoxy containing up to 4 carbon atoms, or a 5- or 6-membered heterocyclic ring containing at least one O, S or N hetero-atom and optionally substituted by halogen, alkyl or alkoxy containing up to 4 carbon atoms or R.sub.2 is further more cyclic alkyl or alkenyl with up to 8 carbon atoms optionally substituted by halogen, dimethylamino, or alkyl, alkoxy or alkylthio with up to 4 carbon atoms; phenyl optionally substituted by halogen, dimethylamino, phenoxy, or alkyl, alkenyl, acyl, alkoxy, alkenoxy or alkynoxy containing up to 4 carbon atoms; or a 5- or 6-membered heterocyclic ring containing at least one O, S or N heteroatom and optionally substituted by halogen, or alkyl or alkoxy containing up to 4 carbon atoms; orR.sup.1 and R.sup.2 together with the adjoining nitrogen atom form a heterocyclic structure optionally substituted by lower alkyl with 1-4 carbon atoms and optionally containing further heteroatoms in addition to nitrogen, andR.sup.3 is straight-chain or branched alkyl, alkenyl or alkynyl each with up to 10 carbon atoms, or cyclic alkyl or alkenyl with up to 8 carbon atoms, optionally substituted by halogen, alkoxy or alkyl-thio containing up to 4 carbon atoms, phenyl, 3,4-methylenedioxyphenyl, cyclic alkyl or alkenyl with up to 8 carbon atoms; phenyl optionally substituted by dioxymethylene or alkyl, alkenyl, alkynyl, alkoxy, alkenoxy, alkynoxy or acyl containing up to 4 carbon atoms; or a heterocyclic ring containing up to 6 atoms of which at least one is O, N or S, which ring is optionally bonded via alkyl containing up to 4 carbon atoms,Which inhibit the metamorphosis of arthropods.

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