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

US4921967A Novel alkylcycloalkyl triazolylmethyl ketones as fungicide intermediates 失效
标题翻译：新型烷基环烷基三唑甲基酮作为杀真菌剂中间体
公开(公告)号：US4921967A
公开(公告)日：1990-05-01
申请号：US54551
申请日：1987-05-27
申请人： Wolfgang Kramer , Manfred Jautelat , Eckart Kranz
发明人： Wolfgang Kramer , Manfred Jautelat , Eckart Kranz
IPC分类号： A01N43/653 , C07C17/26 , C07C43/225 , C07C45/51 , C07C49/327 , C07D249/08 , C07D521/00
CPC分类号： C07D249/08 , A01N43/653 , C07C17/269 , C07C43/225 , C07C45/513 , C07C49/327 , C07D231/12 , C07D233/56 , C07C2101/08
摘要： New alkylcycloalkyl triazolylmethyl ketones of the general formula ##STR1## in which R represents an alkyl group andn is 3, 4, 5, 6 and 7,are produced as described and find use as intermediate products for the preparation of cycloalkyl (.alpha.-triazolyl-.beta.-hydroxy)-ketones, which possess fungicidal and plant growth-regulating properties.
摘要翻译：其中R表示烷基且n为3,4,5,6和7的通式为“IMAGE”（I）的新的烷基环烷基三唑基甲基酮如所述制备，可用作制备环烷基的中间产物（ α-三唑基-β-羟基） - 酮，其具有杀真菌和植物生长调节性质。

2. 发明授权

US4536353A Process for preparing .alpha.-ketonitriles 失效
标题翻译：制备α-酮腈的方法
公开(公告)号：US4536353A
公开(公告)日：1985-08-20
申请号：US667524
申请日：1984-11-02
申请人： Eckart Kranz , Kurt Findeisen
发明人： Eckart Kranz , Kurt Findeisen
IPC分类号： C07C255/40 , C07C67/00 , C07C253/00 , C07C253/30 , C07C255/56 , C07C120/00
CPC分类号： C07C255/00
摘要： A process for preparing an .alpha.-ketonitrile of the formula ##STR1## in which R is optionally substituted aryl, comprising reacting a cyanohydrin of the formula ##STR2## with sulphuryl chloride or thionyl chloride.
摘要翻译：制备式“IMAGE”的α-甲基腈的方法，其中R是任选取代的芳基，包括使下式的氰醇与磺酰氯或亚硫酰氯反应。

3. 发明授权

US4371700A Preparation of 1-azolyl-3,3-dimethyl-1-phenoxy-butan-2-ols 失效
标题翻译： 1-噻唑基-3,3-二甲基-1-苯氧基 - 丁-2-醇的制备
公开(公告)号：US4371700A
公开(公告)日：1983-02-01
申请号：US232461
申请日：1981-02-09
申请人： Eckart Kranz
发明人： Eckart Kranz
IPC分类号： A01N43/50 , A01N43/653 , C07D233/56 , C07D233/60 , C07D233/64 , C07D249/08 , C07D521/00
CPC分类号： C07D231/12 , C07D233/56 , C07D249/08
摘要： A process for the preparation of a 1-azolyl-3,3-dimethyl-1-phenoxy-butan-2-ol of the formula ##STR1## in which X is a nitrogen atom or a CH group,Y each independently is halogen, phenyl, phenoxy, nitro, alkyl, alkoxy or cycloalkyl, andn is 0, 1, 2 or 3,comprising reacting a 1-azolyl-3,3-dimethyl-1-phenoxy-butan-2-one of the formula ##STR2## with formic acid/triethylamine in the form of a 5:2 addition compound of the formula5HCOOHx2N(C.sub.2 H.sub.5).sub.3.The product is a known fungicide.
摘要翻译：制备其中X为氮原子或CH基团的式“IMAGE”的1-吡唑基-3,3-二甲基-1-苯氧基 - 丁-2-醇的方法Y各自独立地为卤素，苯基，苯氧基，硝基，烷基，烷氧基或环烷基，n为0,1,2或3，包括使式（I）的1-吡唑基-3,3-二甲基-1-苯氧基 - 丁-2-酮与甲酸/三乙胺以5:2式5HCOOH 2 N（C 2 H 5）3的加成化合物的形式存在。该产品是已知的杀真菌剂。

4. 发明授权

US4316932A Combating fungi with .alpha.-azolyl-keto derivatives 失效
标题翻译：抗真菌与α-唑基 - 酮衍生物
公开(公告)号：US4316932A
公开(公告)日：1982-02-23
申请号：US54067
申请日：1979-07-02
申请人： Eckart Kranz , Wolfgang Kramer , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
发明人： Eckart Kranz , Wolfgang Kramer , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
IPC分类号： A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D521/00 , A01N43/82
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07D233/56 , C07D249/08
摘要： An .alpha.-azolyl-keto derivative of the formula ##STR1## in which R.sup.1 represents optionally substituted alkyl or optionally substituted phenyl,R.sup.2 represents the grouping --CX.sup.1 X.sup.2 R.sup.3 or alkoxy-carbonyl,R.sup.3 represents halogen, halogenoalkyl or optionally substituted phenyl,R.sup.4 represents the grouping --O--CO--R.sup.5, --O(S)--R.sup.6 or --O--S(O).sub.n --R.sup.7, or alkylamino, dialkylamino, optionally substituted phenylamino or halogen,R.sup.5 represents alkyl, halogenoalkyl, alkenyl, alkynyl, cycloalkyl, optionally substituted phenyl, optionally substituted phenylalkyl, alkylamino, dialkylamino or optionally substituted phenylamino,R.sup.6 represents alkyl, alkenyl, alkynyl, cycloalkyl, optionally substituted phenyl or optionally substituted benzyl,R.sup.7 represents alkyl, halogenoalkyl, optionally substituted phenyl or dialkylamino,n represents 1 or 2,X.sup.1 and X.sup.2 each independently represents hydrogen or halogen, andY represents a nitrogen atom or the CH group, or a physiologically acceptable acid addition salt or metal salt complex thereof, which possesses fungicidal properties.
摘要翻译：其中R 1表示任意取代的烷基或任意取代的苯基，R 2代表基团-CX 1 X 2 R 3或烷氧基 - 羰基，R 3表示卤素，卤代烷基或任意取代的苯基，R 4代表基团 -O-CO-R 5，-O（S）-R 6或-OS（O）n -R 7或烷基氨基，二烷基氨基，任选取代的苯基氨基或卤素，R 5表示烷基，卤代烷基，烯基，炔基，环烷基，任选取代的苯基，任选取代的苯基烷基，烷基氨基，二烷基氨基或任选取代的苯基氨基，R 6表示烷基，烯基，炔基，环烷基，任选取代的苯基或任选取代的苄基，R 7表示烷基，卤代烷基，任选取代的苯基或二烷基氨基，n表示1或2，和X2各自独立地表示氢或卤素，Y表示氮原子或CH基团，或生理上可接受的酸加成盐或金属盐c 其复合物具有杀真菌性能。

5. 发明授权

US4196150A 1-Chloro-3,3-dimethyl-butan-2-one 失效
标题翻译： 1-氯-3,3-二甲基 - 丁-2-酮
公开(公告)号：US4196150A
公开(公告)日：1980-04-01
申请号：US891561
申请日：1978-03-29
申请人： Eckart Kranz , Rudiger Schubart , Herbert Schwarz , Peter Siegle , Heinrich Steude
发明人： Eckart Kranz , Rudiger Schubart , Herbert Schwarz , Peter Siegle , Heinrich Steude
IPC分类号： C07C49/16 , C07C45/00 , C07C45/63 , C07C67/00
CPC分类号： C07C45/63
摘要： A process for preparing monochloropinacoline (1-chloro-3,3-dimethyl-butan-2-one) by contacting a stoichiometric excess of pinacoline with chlorine at a temperature of -20.degree. to +70.degree. C.
摘要翻译：通过在-20℃至+ 70℃的温度下使化学计量过量的对苯乙烯与氯接触来制备单氯代丁酰胺（1-氯-3,3-二甲基 - 丁-2-酮）的方法。

6. 发明授权

US3948893A 1-Phenyl-substituted 1,3,5-triazines 失效
标题翻译： 1-苯基取代的1,3,5-三嗪
公开(公告)号：US3948893A
公开(公告)日：1976-04-06
申请号：US452140
申请日：1974-03-18
申请人： Gerd Aichinger , Axel Haberkorn , Heinrich Kolling , Eckart Kranz , Josef Reisdorff
发明人： Gerd Aichinger , Axel Haberkorn , Heinrich Kolling , Eckart Kranz , Josef Reisdorff
IPC分类号： C07D251/34 , A23K1/16 , A61K31/53 , C07C317/42 , C07C323/44 , C07C323/66 , C07D209/48 , C07D251/04 , C07D251/38 , C07D51/26
CPC分类号： C07D209/48 , A23K20/116 , C07C317/42 , C07C323/44 , C07C323/66
摘要： 1-Phenyl-substituted 1,3,5-triazines of the formula: ##SPC1##And pharmaceutically acceptable nontoxic salts thereof whereinR.sub.1, r.sub.2, r.sub.3, r.sub.4, r.sub.5, r.sub.6, r.sub.7, r.sub.8 and R.sub.9 are the same or different and each is selected from the group consisting of hydrogen, straight or branched chain alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, halogen, nitro, cyano, amino, acylamino, alkoxycarbonylamino, carboxy, alkoxycarbonyl, carbamoyl, acyl, haloacyl, alkylsulphinyl, alkylsulphonyl, haloalkylsulphonyl and sulphamoyl;R.sub.10 is hydrogen, straight or branched chain alkyl, cycloalkyl, haloalkyl, alkoxy, alkoxyalkyl, haloalkoxyalkyl, alkylthioalkyl, haloalkylthioalkyl, alkenyl, alkynyl, alkoxycarbonyl, (alkylthio)carbonyl, (alkylthio)thiocarbonyl, acylamino, diacylamino, amino, dialkylamino, polymethyleneimino, polymethyleneimino interrupted by a heteroatom in the chain, or unsubstituted or substituted benzyl or aryl;R.sub.11 is hydrogen, or alkyl;X is sulphur, sulphinyl, or sulphonyl; andY is oxygen or sulphur,Are useful for their activity against coccidiosis in humans and animals.
摘要翻译：具有下式的1-苯基取代的1,3,5-三嗪：

7. 发明授权

US5081265A Microbicidal substituted dioxolanes 失效
标题翻译：微生物取代的二氧化物
公开(公告)号：US5081265A
公开(公告)日：1992-01-14
申请号：US582581
申请日：1990-09-14
申请人： Hans-Ludwig Elbe , Eckart Kranz , Wilhelm Brandes , Stefan Dutzmann , Gerd Hanssler
发明人： Hans-Ludwig Elbe , Eckart Kranz , Wilhelm Brandes , Stefan Dutzmann , Gerd Hanssler
IPC分类号： C07D317/26 , A01N43/50 , A01N43/653 , C07C45/00 , C07C45/75 , C07C49/245 , C07C49/255 , C07C49/84 , C07C67/00 , C07C323/22 , C07C323/65 , C07D405/00 , C07D407/04 , C07D409/14 , C07D521/00
CPC分类号： C07D231/12 , A01N43/653 , C07D233/56 , C07D249/08
摘要： Fungicidal dioxolanes of the formula ##STR1## in which R.sup.1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkinyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted aryl, optionally substituted aryloxy, optionally substituted arylthio, optionally substituted arylsulphinyl, optionally substituted arylsulphonyl, optionally substituted arylalkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted arylsulphinylalkyl, optionally substituted arylsulphonylalkyl, optionally substituted aralkyloxyalkyl, optionally substituted aralkylthioalkyl, optionally substituted aralkylsulphinylalkyl or optionally substituted aralkylsulphonylalkyl,R.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6 independently of one another represent hydrogen, alkyl or cycloalkyl, orR.sup.3 and R.sup.4 together represent divalent alkanediyl and/orR.sup.5 and R.sup.6 together represent divalent alkanediyl andA represents nitrogen or a CH group,and addition products thereof with acids and metal salts. Also novel intermediates of the formulas ##STR2##

8. 发明授权

US5076833A Herbicidal and plant growth-regulating 6-(pent-3-yl)-1,2,4-triazin-5(4H)-ones 失效
标题翻译：除草剂和植物生长调节6-（PENT-3-YL）-1,2,4-三嗪-5（4H） - 酮
公开(公告)号：US5076833A
公开(公告)日：1991-12-31
申请号：US517262
申请日：1990-05-01
申请人： Eckart Kranz , Karl-Julius Reubke , Klaus Lurssen , Hans-Joachim Santel , Robert R. Schmidt , Birgit Krauskopf
发明人： Eckart Kranz , Karl-Julius Reubke , Klaus Lurssen , Hans-Joachim Santel , Robert R. Schmidt , Birgit Krauskopf
IPC分类号： C07D253/06 , A01N43/707 , C07D253/075
CPC分类号： C07D253/075 , A01N43/707
摘要： A herbicidal or plant growth-regulating 6-(pent-3-yl)-1,2,4-triazin-5(4H)-one of the formula ##STR1## in which R.sup.1 represents amino andR.sup.2 represents alkylthio having more than 1 carbon atom, alkylamino or dialkylamino,orR.sup.1 represents methylamino andR.sup.2 represents alkylthio.
摘要翻译：式（I）的除草或植物生长调节6-（戊-3-基）-1,2,4-三嗪-5（4H） - 酮，其中R 1表示氨基，R 2表示具有多于1个碳原子，烷基氨基或二烷基氨基，或R 1表示甲基氨基，R 2表示烷硫基。

9. 发明授权

US4988715A Microbicidal substituted dioxolanes 失效
标题翻译：杀菌剂取代二氧戊环
公开(公告)号：US4988715A
公开(公告)日：1991-01-29
申请号：US389032
申请日：1989-08-03
申请人： Hans-Ludwig Elbe , Eckart Kranz , Wilhelm Brandes , Stefan Dutzmann , Gerd Hanssler
发明人： Hans-Ludwig Elbe , Eckart Kranz , Wilhelm Brandes , Stefan Dutzmann , Gerd Hanssler
IPC分类号： C07D317/26 , A01N43/50 , A01N43/653 , C07C45/00 , C07C45/75 , C07C49/245 , C07C49/255 , C07C49/84 , C07C67/00 , C07C323/22 , C07C323/65 , C07D405/00 , C07D407/04 , C07D409/14 , C07D521/00
CPC分类号： C07D231/12 , A01N43/653 , C07D233/56 , C07D249/08
摘要： Fungicidal dioxolanes of the formula ##STR1## in which R.sup.1 represents optionally substituted alkyl, or other radicalsR.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6 independently of one another represent hydrogen, alkyl or cycloalkyl, orR.sup.3 and R.sup.4 together represent divalent alkanediyl and/orR.sup.5 and R.sup.6 together represent divalent alkanediyl andA represents nitrogen or a CH group,and addition products thereof with acids and metal salts. Also novel intermediates of the formulas ##STR2##
摘要翻译：其中R 1表示任选取代的烷基或其它基团R 2，R 3，R 4，R 5和R 6彼此独立地表示的式（I）的杀真菌二氧戊环代表氢，烷基或环烷基，或者R 3和R 4一起代表二价烷二基和/或R 5和R 6一起表示二价烷二基，A表示氮或CH基，并且其与酸和金属盐的加成产物。（VIa）（VIIa）（VIIa）（VIIa）（VIIa）（VIIa）中的新颖的中间体

10. 发明授权

US4530715A Cycloalkyl (.alpha.-triazolyl-.beta.-hydroxy)-ketones as fungicides and plant growth regulators 失效
标题翻译：环烷基（α-三唑基-β-羟基） - 酮作为杀真菌剂和植物生长调节剂
公开(公告)号：US4530715A
公开(公告)日：1985-07-23
申请号：US438448
申请日：1982-11-02
申请人： Eckart Kranz , Karl H. Buchel , Udo Kraatz , Erik Regel , Wilhelm Brandes , Paul-Ernst Frohberger , Klaus Lurssen
发明人： Eckart Kranz , Karl H. Buchel , Udo Kraatz , Erik Regel , Wilhelm Brandes , Paul-Ernst Frohberger , Klaus Lurssen
IPC分类号： A01N43/653 , C07C45/63 , C07D249/08 , C07D521/00 , A01N43/64 , A01N55/02 , C07F3/00
CPC分类号： C07D231/12 , A01N43/653 , C07C45/63 , C07D233/56 , C07D249/08
摘要： Cycloalkyl (.alpha.-triazolyl-.beta.-hydroxy)-ketones of the general formula ##STR1## in which R.sup.1 represents an optionally substituted cycloalkyl group, andR.sup.2 represents a halogenoalkyl, halogenoalkenyl or alkoxycarbonyl group,and their physiologically acceptable acid addition salts and metal salt complexes are new, are prepared as described and find use as fungicides and plant growth regulators.
摘要翻译：其中R 1表示任选取代的环烷基，R 2表示卤代烷基，卤代烯基或烷氧基羰基，以及它们的生理上可接受的酸加成盐（Ⅰ）所示的环烷基（α-三唑基-β-羟基） - 酮和金属盐络合物是新的，按照描述制备并用作杀真菌剂和植物生长调节剂。

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