CAS: 62865-36-5; Diclomezine

该化合物是一种化学化合物,被归类为抗心胺,主要用于抗乳性特性,以缓解运动疾病和恶心的症状;其功能是阻塞体内的异丁胺受体,这有助于减少恶心和呕吐的感知;二氯甲胺酮通常以口服方式施用,并因其镇静作用相对较低而为人所知,因为与其他抗心胺药物相比,其镇静作用相对较低,使该化合物成为某些病人的首选;该化合物在水中具有中等溶性,并且更易溶于有机溶剂,从而影响其配药的配方;其化学结构包括苯并氮酸,有助于其药剂活动;与许多药物一样,潜在副作用可能包括疏松,干口和眩晕,用户必须就使用该物质咨询保健专业人员,特别是与其他药物一起咨询.

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CAS号62938-71-0 6-(3,5-dichloro...

合成工艺路线路线简述

  • 合成目标产物 Diclomezine 主要起始原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
  • (文献来源)合成步骤主要原料 Ethanamine, N-[(3,5-Dichlorophenyl)Methylene]-2,2-Diethoxy-
📜6-(3,5-Dichloro-4-Methylphenyl)-4-Methylthio-4,5-Dihydro-3(2H)-Pyridazinone置于盐酸体系中,用 Sodium Hydroxide 作为反应溶剂,以94%的收率获得产物哒菌清
参考文献:Process For Producing Antifungal Oyridazinone Derivatives
标题:Process For Producing Antifungal Oyridazinone Derivatives
摘要:公式(i)的化合物:其中r.Sup.1和r.Sup.3代表氢或卤素原子,R.Sup.2代表氢或卤素原子或较低的烷基或烷氧基(假设r.Sup.1,R.Sup.2和r.Sup.3不同时为氢),表示单个或双碳-碳键,其中为单键时,R.Sup.4代表--Sr.Sup.5的基团(其中r.Sup.5表示可选择取代的烷基,苯基,芳基烷基或吡啶基团或较低的烯基团),为双键时,R.Sup.4代表氢]可以通过将公式(II)的化合物与公式r.Sup.6 H的化合物反应而制备:其中r.Sup.6代表--Sr.Sup.5的基团,--Sr.Sup.7的基团(其中r.Sup.7代表##str3##的基团,Y代表氧或硫,R.Sup.8和r.Sup.9代表较低的烷氧基,R.Sup.10代表较低的烷氧基,较低的烷基或苯基),甲氧基基团或卤素原子],以得到公式(iv)的化合物:或者,其中r.Sup.6代表甲氧基基团,为其甲酯;将该化合物与肼反应得到公式(v)的化合物:并且如有必要,用酸或碱处理公式(v)的化合物以产生公式(vi)的化合物.所有公式(i)的化合物都是有价值的抗真菌剂,其中r.Sup.6代表--Sr.Sup.5的化合物的公式(v)是新颖的化合物.

海关参考信息

专利信息


专利号:WO-2025056767-A1
优先权日:2023-09-15
标题 :Process for the preparation of enantiomerically enriched aliphatic amines
发明人:BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS
权利人:SYNGENTA CROP PROTECTION AG
摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.

专利号:US-2016073631-A1
优先权日:2013-03-04
标 题 :Process for the preparation of dihydropyrrole derivatives
发明人:EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS
权利人:SYNGENTA PARTICIPATIONS AG; SYNGENTA LTD
摘要:The present invention provides stereoselective processes for the preparation of compounds of formula (I) n n n n n n n n n n n n wherein n P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; n R 1 is chlorodifluoromethyl or trifluoromethyl; n R 2 is optionally substituted aryl or optionally substituted heteroaryl; n n is 0 or 1; n including the process comprising n (a-i) reacting a compound of formula II n n n n n n n n n n n n n n n n wherein P, R 1 and R 2 are as defined for the compound of formula I; n with nitromethane in the presence a chiral catalyst to give a compound of formula III n n n n n n n n n n n n n n n n wherein P, R 1 and R 2 are as defined for the compound of formula I; and n (a-ii) reductively cyclising the compound of formula III to give the compound of formula I. n n n n n The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).

专利号:US-9233920-B2
优先权日:2010-06-11
标题 :Process for the preparation of dihydropyrrole derivatives
发明人:EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS
权利人:EL QACEMI MYRIEM; SMITS HELMARS; CASSAYRE JEROME YVES; MULHOLLAND NICHOLAS PHILLIP; RENOLD PETER; GODINEAU EDOUARD; PITTERNA THOMAS; SYNGENTA PARTICIPATIONS AG; SYNGENTA LTD
摘要:The present invention provides stereoselective processes for the preparation of compounds of formula (I) wherein P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; R 1 is chlorodifluoromethyl or trifluoromethyl; R 2 is optionally substituted aryl or optionally substituted heteroaryl; n is 0 or 1; including the process comprising (a-i) reacting a compound of formula II wherein P, R 1 and R 2 are as defined for the compound of formula I; with nitromethane in the presence a chiral catalyst to give a compound of formula III Wherein P, R 1 and R 2 are as defined for the compound of formula I; and (a-ii) reductively cyclizing the compound of formula III to give the compound of formula I. The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).

专利号:US-10906880-B2
优先权日:2016-01-26
标题:Kind of isothiazole oxime ether-containing strobilurin derivatives and its preparation methods and application
发明人:FAN ZHIJIN; CHEN LAI; GUO XIAOFENG; ZHU YUJIE; QIAN XIAOLIN; MA LIUYONG; ZHANG NAILOU; WANG HAIXIA; ZHANG ZHIMING; XU JINGHUA; SONG YINQI
权利人:UNIV NANKAI
摘要:The present invention is that provided a synthesis method of a series of isothiazole oxime ether containing strobilurin derivatives IV. The present invention relates to 3,4-dichloroisothiazolyl oxime ether strobilurin derivatives, and their chemical structural formula is as shown by IV. n n n n n n n n n n The invention discloses the structural formula of the above compound, the synthesis method and the use as an insecticide, a fungicide, an anti-plant virus agent, and an agriculturally acceptable auxiliary or synergist and a commercial insecticide. The use of a fungicide, an anti-plant virus agent and an acaricide in combination for controlling agricultural, forestry, horticultural plant pests, diseases, virus diseases and preparation methods.

专利号:US-9968097-B2
优先权日:2012-05-30
标题:Composition comprising a biological control agent and a fungicide selected from inhibitors of the lipid membrane synthesis, the melanine biosynthesis, the nucleic acid synthesis or the signal transduction
发明人:WACHENDORFF-NEUMANN ULRIKE; ANDERSCH WOLFRAM; STENZEL KLAUS; SPRINGER BERND
权利人:BAYER CROPSCIENCE AG
摘要:The present invention relates to a composition comprising at least one biological control agent. Furthermore, the present invention relates to the use of this composition as well as a method for reducing overall damage of plants and plant parts.

专利号:US-2007232495-A1
优先权日:2006-03-24
标题:Compositions and methods to add value to plant products, increasing the commercial quality, resistance to external factors and polyphenol content thereof
发明人:NAPPA ALVARO O; LORENZINI FELIPE C; SANHUEZA ANDRES L
权利人:NAPPA ALVARO O; LORENZINI FELIPE C; SANHUEZA ANDRES L
摘要:The invention is related to compositions and methods that naturally protect plant tissues against ultraviolet radiation and temperature, thus giving protection against sunburn to plants, plant parts, fruits and/or flowers during their development. The invention is also related to compositions and methods to naturally improve the color of plants, plant parts, fruits and/or flowers by inducing the natural synthesis of flavonoids and anthocyanins present in plants. Likewise, the present invention is directed to improving the nutritional value of plants, plant parts, fruits and/or flowers by increasing the normal levels of polyphenolic compounds, especially flavonoids, present therein. Additionally, the present invention is related to compositions and methods that give more resistance to plants, plant parts, fruits and/or flowers against pathogens as bacteria and fungi. Finally, the present invention is related to plants, plant parts, fruits, flowers and/or propagating material treated with the compositions described in the present document.

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主要参考文献


1: Kim H, Kim TH, Kim J, Park KM. Diclomezine: 6-(3,5-dichloro-4-methyl-phen- yl)pyridazin-3(2H)-one. Acta Crystallogr Sect E Struct Rep Online. 2010 Nov 20;66(Pt 12):o3257. doi: 10.1107/S1600536810047409.

合成参考文献


参考文献:10.1107/s1600536810047409
摘要:Kim H, Kim TH, Kim J, Park KM. Diclomezine: 6-(3,5-dichloro-4-methyl-phen-yl)pyridazin-3(2H)-one. Acta Crystallogr Sect E Struct Rep Online. 2010 Nov 20;66(Pt 12):o3257.
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