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公开(公告)号:US4945186A
公开(公告)日:1990-07-31
申请号:US455782
申请日:1990-01-02
申请人: Shinichi Matsuura , Osamu Miyano
发明人: Shinichi Matsuura , Osamu Miyano
IPC分类号: B01J27/125 , C07C45/00 , C07C45/63 , C07C47/55 , C07C67/00
CPC分类号: C07C45/63
摘要: A method of producing 3-bromobenzaldehyde is disclosed, wherein, upon producing 3-bromobenzaldehyde by allowing benzaldehyde to react with bromine in the presence of brominating catalyst in 1,2-dichloroethane being a reaction solvent, 1,2-dichloroethane having been used for aforesaid reaction as a reaction solvent is recovered and, after the recovered solvent is allowed first to react with chlorine in the presence of above brominating catalyst, the reaction is performed by the addition of benzaldehyde and bromine. Foregoing 1,2-dichloroethane recovered may be brought to the reaction with chlorine with or without adding fresh 1,2-dichloroethane and above brominating catalyst is preferably aluminum chloride.
摘要翻译: 公开了一种生产3-溴苯甲醛的方法,其中在溴代催化剂存在下,在1,2-二氯乙烷为反应溶剂中,通过使苯甲醛与溴反应生成3-溴苯甲醛时,将1,2-二氯乙烷用于 回收作为反应溶剂的上述反应,在回收的溶剂首先在上述溴化催化剂存在下与氯反应后,通过加入苯甲醛和溴进行反应。 回收的前述1,2-二氯乙烷可与带有或不加入新鲜的1,2-二氯乙烷的氯反应,并且上述溴化催化剂优选为氯化铝。
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公开(公告)号:US4937388A
公开(公告)日:1990-06-26
申请号:US114038
申请日:1987-10-29
IPC分类号: A01N31/04 , A01N31/14 , A01N33/10 , A01N37/00 , A01N43/08 , A01N43/30 , A01N43/40 , A01N47/02 , C07C43/225 , C07C43/23 , C07C43/29 , C07C43/295 , C07C45/60 , C07C45/63 , C07C47/546 , C07C47/55 , C07C47/575 , C07C49/813 , C07C49/84 , C07C67/02 , C07D213/30 , C07D303/08 , C07D303/22 , C07D307/38 , C07D307/42 , C07D317/54
CPC分类号: C07D213/30 , A01N31/04 , A01N31/14 , A01N33/10 , A01N37/00 , A01N43/08 , A01N43/30 , A01N43/40 , A01N47/02 , C07C317/00 , C07C323/00 , C07C43/225 , C07C43/23 , C07C43/29 , C07C43/295 , C07C45/60 , C07C45/63 , C07C47/546 , C07C47/55 , C07C47/575 , C07C49/813 , C07C49/84 , C07D303/08 , C07D303/22 , C07D307/38 , C07D307/42 , C07D317/54
摘要: The invention provides insecticidally active compounds of formula I: ##STR1## wherein A is selected from oxygen and a group of formula S(O).sub.n, where n represents 0, 1 or 2; W represents one or two substituents selected from halo, alkyl, alkoxy, alkoxyalkyl, haloalkyl and haloalkoxy, or W represents a bidentate group linking adjacent carbon atoms, selected from alkylene and alkylenedioxy; Y represents a substituted aryl group where each substituent is selected from halo, alkyl, aryl, aralkyl, aryloxy and arylamino; Z represents a fluoroalkyl group of up to two carbon atoms; and either X' represents hydrogen and X is selected from hydrogen, halo, hydroxy, alkoxy and acyloxy, or X and X' together represent a second bond between the adjacent carbon atoms.The invention also provides processes and intermediates useful for the preparation of the compounds of formula I, insecticidal compositions comprising the compounds of formula I, and methods of combating and controlling pests therewith.
摘要翻译: 本发明提供了杀虫活性的式I化合物:其中A选自氧和式S(O)n基团,其中n表示0,1或2; W表示选自卤素,烷基,烷氧基,烷氧基烷基,卤代烷基和卤代烷氧基的一个或两个取代基,或W表示连接相邻碳原子的二齿基团,选自亚烷基和亚烷基二氧基; Y表示取代的芳基,其中每个取代基选自卤素,烷基,芳基,芳烷基,芳氧基和芳基氨基; Z表示最多2个碳原子的氟代烷基; 并且X'表示氢,X选自氢,卤素,羟基,烷氧基和酰氧基,或X和X'一起表示相邻碳原子之间的第二键。 本发明还提供了可用于制备式I化合物的方法和中间体,其包含式I化合物的杀虫组合物,以及与其对抗和控制害虫的方法。
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公开(公告)号:US4937253A
公开(公告)日:1990-06-26
申请号:US248770
申请日:1988-09-23
IPC分类号: A61K31/165 , A61K31/19 , A61K31/215 , A61K31/275 , A61K31/415 , A61P29/00 , A61P37/08 , A61P43/00 , C07C45/29 , C07C45/44 , C07C45/56 , C07C45/62 , C07C45/67 , C07C45/68 , C07C45/71 , C07C47/542 , C07C47/546 , C07C47/548 , C07C47/55 , C07C47/575 , C07C255/33 , C07C323/25 , C07C323/41 , C07C323/52 , C07C323/56 , C07C323/60 , C07C323/66 , C07C323/67 , C07D233/84 , C07D233/90 , C07D257/04 , C07D303/40 , C07D303/48 , C07D307/38 , C07D307/54 , C07D309/30 , C07D333/24 , C07D401/12
CPC分类号: C07D257/04 , A61K31/19 , C07C255/33 , C07C323/56 , C07C323/60 , C07C323/66 , C07C323/67 , C07C45/298 , C07C45/44 , C07C45/56 , C07C45/62 , C07C45/673 , C07C45/68 , C07C45/71 , C07C47/542 , C07C47/546 , C07C47/548 , C07C47/55 , C07C47/575 , C07D233/84 , C07D233/90 , C07D303/40 , C07D303/48 , C07D307/38 , C07D307/54 , C07D309/30
摘要: This invention relates to ester prodrugs for alkanoic acid compounds useful as leukotriene antagonists, and pharmaceutical compositions containing such ester prodrug compounds. This invention also relates to methods of treating diseases in which leukotrienes are a factor by administration of an effective amount of the above compounds or compositions.
摘要翻译: 本发明涉及可用作白三烯拮抗剂的链烷酸化合物的酯前药,以及含有这种酯前药化合物的药物组合物。 本发明还涉及通过施用有效量的上述化合物或组合物治疗白三烯是一个因素的疾病的方法。
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公开(公告)号:US4868209A
公开(公告)日:1989-09-19
申请号:US97827
申请日:1987-09-17
申请人: Nazim Punja
发明人: Nazim Punja
IPC分类号: A01N53/00 , A01N53/06 , C07C17/14 , C07C17/26 , C07C29/10 , C07C29/14 , C07C29/147 , C07C43/174 , C07C43/178 , C07C43/225 , C07C43/23 , C07C45/00 , C07C47/55 , C07C51/15 , C07C63/68 , C07C63/70 , C07C63/72 , C07C63/74 , C07C69/743 , C07C229/38 , C07D309/12
CPC分类号: C07C17/14 , A01N53/00 , C07C17/269 , C07C229/38 , C07C317/00 , C07C323/00 , C07C43/1742 , C07C43/1786 , C07C43/225 , C07C43/23 , C07C45/00 , C07C47/55 , C07C51/15 , C07C63/68 , C07C63/70 , C07C63/72 , C07C63/74 , C07C69/747 , C07D309/12
摘要: Compounds of formula I wherein R.sup.1 and R.sup.2 are haloalkyl or halo, X is O, S, S(O), SO.sub.2 or NR.sub.4 where R.sub.4 is H or alkyl, R.sup.3 is alkyl and n is 1 to 4, and compositions comprising them, useful as insecticides. ##STR1##
摘要翻译: 式Ⅰ化合物,其中R 1和R 2为卤代烷基或卤素,X为O,S,S(O),SO 2或NR 4,其中R 4为H或烷基,R 3为烷基,n为1至4, 作为杀虫剂。 (一)
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公开(公告)号:US4845304A
公开(公告)日:1989-07-04
申请号:US190087
申请日:1988-05-04
申请人: Yasuo Yoshida , Yoshikazu Kimura
发明人: Yasuo Yoshida , Yoshikazu Kimura
摘要: A process for producing a fluorobenzaldehyde of the formula: ##STR1## wherein X is a chlorine atom, a bromine atom or an iodine atom, n is an integer of from 1 to 5, and m is an integer of from 1 to 5, provided n.gtoreq.m, which comprises reacting a halogenated benzaldehyde of the formula: ##STR2## wherein X and n are as defined above, with a metal fluoride in the presence of a catalyst, wherein at least one member selected from the group consisting of quaternary phosphonium salts and quaternary ammonium salts is used as the catalyst.
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公开(公告)号:US4804785A
公开(公告)日:1989-02-14
申请号:US97113
申请日:1987-09-16
申请人: Bernd Janssen , Stefan Karbach , Hans-Gert Recker , Marco Thyes
发明人: Bernd Janssen , Stefan Karbach , Hans-Gert Recker , Marco Thyes
IPC分类号: C07C47/238 , C07C45/00 , C07C45/51 , C07C47/21 , C07C47/22 , C07C47/228 , C07C47/232 , C07C47/24 , C07C47/277 , C07C67/00 , C07D301/12 , C07D303/14 , C07D303/16 , C07D303/32 , C07C47/55 , C07C47/546
CPC分类号: C07D303/16 , C07C205/44 , C07C45/515 , C07C47/21 , C07C47/232 , C07C47/24 , C07C47/277 , C07D303/14
摘要: Alpha,beta-substituted acroleins of the general formula I ##STR1## where A and B are identical or different and are each C.sub.1 -C.sub.4 -alkyl, naphthyl, biphenyl or phenyl which may be monosubstituted or polysubstituted by halogen, nitro, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl, phenoxy or phenylsulfonyl, are prepared by a process in which a compound of the general formula III ##STR2## where A has the above meanings and R.sup.1 and R.sup.2 are identical or different and are each C.sub.1 -C.sub.4 -alkyl or together possess the carbon atoms required to complete a ring, is reacted with a phosphorus compound of the general formula IV or V ##STR3## where B the meanings stated above, R.sup.1 and R.sup.2 are as defined above and X.sup..crclbar. is a halide ion, in the presence of a base. The alpha,beta-substituted acroleins can be further processed to give hydroxymethyloxiranes.
摘要翻译: α,β取代的通式I(I)的丙烯醛,其中A和B是相同或不同的并且各自是可被卤素,硝基, C 1 -C 4 - 烷基,C 1 -C 4 - 烷氧基,C 1 -C 4卤代烷基,苯氧基或苯基磺酰基,其中A为具有上述含义的通式III(III)的化合物和R 1 和R 2相同或不同,并且各自为C 1 -C 4烷基或一起具有完成环所需的碳原子,与通式IV或V的磷化合物反应(V) )其中B为上述含义,R1和R2如上所定义,X( - )为卤素离子,在碱的存在下。 α,β-取代的丙烯醛可以进一步加工得到羟基甲基环氧乙烷。
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公开(公告)号:US4748257A
公开(公告)日:1988-05-31
申请号:US887471
申请日:1986-07-21
申请人: Rainer Fuchs , Fritz Maurer , Uwe Priesnitz , Hans-Jochem Riebel , Erich Klauke
发明人: Rainer Fuchs , Fritz Maurer , Uwe Priesnitz , Hans-Jochem Riebel , Erich Klauke
IPC分类号: C07B61/00 , C07C41/00 , C07C41/48 , C07C41/50 , C07C43/313 , C07C43/315 , C07C45/00 , C07C45/29 , C07C45/30 , C07C45/59 , C07C45/63 , C07C47/55 , C07C47/575 , C07C67/00 , C07D317/16 , C07D317/22 , C07D319/06 , C07C43/303
CPC分类号: C07D317/22 , C07C45/292 , C07C45/305 , C07C45/59 , C07C45/63 , C07C47/55 , C07C47/575 , C07D317/16
摘要: The new compound ##STR1## is prepared and converted to the new acetal ##STR2## which is reacted with an alkali phenolate or alkaline earth metal phenolate in the presence of copper or a copper compound as a catalyst and in the presence of a diluent at a temperature between about 100.degree. and 200.degree. C. to produce the new acetal ##STR3## which can be hydrolyzed to the corresponding aldehyde which is a known intermediate for pyrethroid-like insecticides.
摘要翻译: 制备新的化合物< IMAGE>并将其转化成新的缩醛< IMAGE>其在铜或铜化合物作为催化剂的存在下与碱性酚盐或碱土金属酚盐反应,并在稀释剂 温度在约100℃至200℃之间,以产生可以水解成相似的醛的新的缩醛“IMAGE”,其是拟除虫菊酯类杀虫剂的已知中间体。
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公开(公告)号:US4736065A
公开(公告)日:1988-04-05
申请号:US908611
申请日:1986-09-17
IPC分类号: A01N37/18 , A01N39/02 , A01N43/12 , A01N45/02 , C07C33/46 , C07C43/166 , C07C43/168 , C07C43/176 , C07C45/30 , C07C45/51 , C07C47/24 , C07C47/277 , C07C47/55 , C07C233/09 , C07D307/91 , C07D309/12 , C07F9/40 , C07F9/54 , C07C103/22
CPC分类号: C07D307/91 , A01N37/18 , A01N39/02 , A01N43/12 , A01N45/02 , C07C33/46 , C07C43/166 , C07C43/168 , C07C43/176 , C07C45/305 , C07C45/513 , C07C47/24 , C07C47/277 , C07C47/55 , C07D309/12 , C07F9/4015 , C07F9/5428 , C07C2103/18 , C07C2103/26
摘要: A compound of Formula I: ##STR1## wherein: Ar represents a polynuclear carboxyclic or heterocyclic fused ring system having at least one carbocylic or heterocyclic ring of aromatic character, the polynuclear ring system optionally carrying one or more of the substituents halogen, C.sub.1 -C.sub.6 alkyl --CF.sub.3, or --OCF.sub.y H.sub.3-y, wherein y is 0-3;n is 0 or 1 and m is 1-11Z represents a group of Formula: ##STR2## wherein: R.sub.A and R.sub.B which may be identical or different each represent hydrogen or methyl;R.sub.C represents methyl;R.sub.D represents methyl, ethyl, n-propyl, isopropyl, t-butyl, or vinyl; andR.sub.E represents hydrogen or methyl or wherein:R.sub.C and R.sub.D together with C.sub..beta. form a cyclopropane or a cyclobutane ring or goether form a methylene group (.dbd.CH.sub.2) or wherein:R.sub.A and R.sub.B together with C.sub..alpha. and C.sub..beta. form a cyclobutane ring.
摘要翻译: 式I的化合物:其中:Ar表示具有至少一个具有芳族特征的碳环或杂环的多核羧基或杂环稠环体系,所述多核环系统任选地携带一个或多个取代基卤素,C 1 -C6烷基-CF3或-OCFyH3-y,其中y为0-3; n为0或1,m为1-11 Z表示下式的基团:其中:RA和RB可以相同或不同,各自表示氢或甲基; RC代表甲基; RD表示甲基,乙基,正丙基,异丙基,叔丁基或乙烯基; 并且RE表示氢或甲基,或其中:RC和RD与Cβ一起形成环丙烷或环丁烷环或乙醚形成亚甲基(= CH 2),或其中:RA和RB与C 1和C 2一起形成环丁烷环 。
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公开(公告)号:US4588844A
公开(公告)日:1986-05-13
申请号:US575962
申请日:1984-02-01
申请人: Ernst Kysela , Erich Klauke
发明人: Ernst Kysela , Erich Klauke
IPC分类号: C07C45/00 , C07C45/28 , C07C45/56 , C07C47/52 , C07C47/542 , C07C47/55 , C07C47/565 , C07C47/575 , C07C47/58 , C07C67/00 , C07C313/00 , C07C319/20 , C07C323/22 , C07C45/42
CPC分类号: C07C323/00 , C07C45/565 , C07C47/55 , C07C47/575
摘要: Aromatic aldehydes are prepared by formylating the corresponding aromatic compounds with urotropine in the presence of hydrogen fluoride. By the described process certain new aromatic aldehydes can be prepared.
摘要翻译: 通过在氟化氢存在下,用乌洛托品甲酰化相应的芳族化合物来制备芳族醛。 通过描述的方法,可以制备某些新的芳族醛。
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公开(公告)号:US4578522A
公开(公告)日:1986-03-25
申请号:US650981
申请日:1984-09-14
申请人: John F. Eaddy, III
发明人: John F. Eaddy, III
CPC分类号: C07F15/006 , C07C45/513 , C07C47/55 , C07C51/00 , C07C51/16
摘要: This invention relates to a method of synthesis of certain substituted carboxylic acids useful in lowering serum triglyceride and total cholesterol levels in mammals (including man) represented by the general formula I:Ar.sup.1 --Ar.sup.2 (I)whereinAr.sup.1 is selected from ##STR1## Ar.sup.2 is selected from ##STR2## and R is selected from C.sub.1-5 alkyl, halogen, perhalo-C.sub.1-4 alkyl, C.sub.1-4 alkoxy, phenyl, C.sub.1-4 acyl, C.sub.1-6 alkoxycarbonyl, amino or hydroxy.
摘要翻译: 本发明涉及一种合成某些通式I所示哺乳动物(包括人)中血清甘油三酯和总胆固醇水平的取代羧酸的方法:Ar1-Ar2(I)其中Ar1选自Ar2 选自
,R选自C 1-5烷基,卤素,全卤代-C 1-4烷基,C 1-4烷氧基,苯基,C 1-4酰基,C 1-6烷氧基羰基,氨基或羟基。
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