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

US3703526A Novel 3-(3,5-dichlorophenyl)oxazolidine-2,4-dione derivatives 失效
标题翻译：新的3-（3,5-二氯苯基）氧杂环丁烷-2,4-二酮衍生物
公开(公告)号：US3703526A
公开(公告)日：1972-11-21
申请号：US3703526D
申请日：1970-11-16
申请人： SUMITOMO CHEMICAL CO , HOKKO CHEM IND CO
发明人： SATO KATSUMI , NAKAMURA TAKASHI , NAKAMURA MASARU , HIRASAWA KAZUO , HAMADA MATSUO , TAKAHASHI KENZI , YASHIMA MASAAKI , OZAKI TOSHIAKI , YAMAMOTO SIGEO , OOISHI TADASHI , FUJINAMI AKIRA , HORIUCHI FUKASHI , NODERA KATSUJI
IPC分类号： C07D263/44 , C07D85/34
CPC分类号： C07D263/44
摘要： AN OXAZOLIDINEIDIONE OF THE FORMULA:

2,4-DI(O=),2-(3,5-DI(CL-)PHENYL),5-R1,5-R2-OXAZOLIDINE

WHEREIN R1 AND R2 ARE EACH A HYDROGEN ATOM OR A LOWER ALKYL GROUP, IS PREPARED BY REACTING 3,5-DICHLOROPHENYL ISOCYANATE WITH ALKYL A-HYDROXYALKANOATE IN THE PRESENCE OF A TERTIARY ORGANIC AMINE OR ALTERNATIVELY REACTING 3,5DICHLOROANILENE, DIALKYL CARBONATE ANDA IKYL A-HYDROXYALKANOATE IN THE PRESENCE OF AN ALKALI METAL ALKOXIDE. THE OXAZOLIDINEDIONE IS USEFUL AS AN ANTI-FUNGAL AGENT AGAINST A VARIETY OF PHYTOPATHOGENIC FUNGI.

2. 发明专利

CA927395A 3-(3,5-DICHLOROPHENYL) IXAZOLIDINE-2,4-DIONE DERIVATIVES 未知
公开(公告)号：CA927395A
公开(公告)日：1973-05-29
申请号：CA122162
申请日：1971-09-07
申请人： SUMITOMO CHEMICAL CO , HOKKO CHEM IND CO
发明人： OZAKI TOSHIAKI , TAKAHASHI KENZI , HIRASAWA KAZUO , YAMAMOTO SIGEO , NODERA KATSUJI , YASHIMA MASAAKI , FUJINAMI AKIRA , NAKAMURA MASARU , NAKAMURA TAKASHI , SATO KATSUMI , HAMADA MITUO , HORIUCHI FUKASHI , OOISHI TADASHI

3. 发明专利

DE1811843A1 未知
公开(公告)号：DE1811843A1
公开(公告)日：1969-07-03
申请号：DE1811843
申请日：1968-11-28
申请人： SUMITOMO CHEMICAL CO , HOKKO CHEM IND CO
发明人： SATO KATSUMI , NAKAMURA MASARU , TAKAHASHI KENZI , YASHIMA MASAAKI , HIRASAWA KAZUO , OZAKI TOSHIAKI , YAMAMOTO SIGEO , OOISHI TADASHI , FUJINAMI AKIRA , HORIUCHI FUKASHI , NODERA KATSUJI
IPC分类号： C07D263/44 , C07D85/34

4. 发明专利

CA926407A 3-(3,4-CICHLOROPHENYL) OXAZOLIDINE-2,4-DIONE DERIVATIVES 未知
公开(公告)号：CA926407A
公开(公告)日：1973-05-15
申请号：CA36033
申请日：1968-11-25
申请人： HOKKO CHEM IND CO , SUMITOMO CHEMICAL CO
发明人： NAKAMURA TAKASHI , HIRASAWA KAZUO , HAMADA MITUO , YAMAMOTO SIGEO , FUJINAMI AKIRA , HORIUCHI FUKASHI , NAKAMURA MASARU , OOISHI TADASHI , YASHIMA MASAAKI , TAKAHASHI KENZI , OZAKI TOSHIAKI , NODERA KATSUJI , SATO KATSUMI
IPC分类号： C07D263/44

5. 发明授权

US3865866A Carbamic acid esters 失效
标题翻译：氨基甲酸酯
公开(公告)号：US3865866A
公开(公告)日：1975-02-11
申请号：US10962271
申请日：1971-01-25
申请人： SUMITOMO CHEMICAL CO
发明人： OZAKI TOSHIAKI , KAMOSHITA KATSUZO , TANAKA KATSUTOSHI , YAMAMOTO SIGEO , OOISHI TADASHI , NAKAI SHINJI , AKIBA KEIICHIRO
IPC分类号： A01N47/22 , A01P3/00 , C07C79/46 , C07C101/00
CPC分类号： A01N47/22
摘要： A carbamic acid ester, which is useful as fungicidal agent, having the formula (I)

wherein R1 is a halogen atom or a nitro, lower alkyl, lower alkoxy, lower alkylthio, cyano, sulfonamide, lower alkylsulfinyl or lower alkylsulfonyl group, and groups represented by R1m1 may be same or different; m1 is an integer of 1 to 5; and X is a furyl or thienyl group or a group of the formula,

WHEREIN Y is an oxygen or sulfur atom; R2 is a hydrogen atom, a halogen atom, an alkyl group or an alkoxy group; m2 is an integer of 1 to 5; and n is 0 or 1. The compound is produced by I. REACTING A PHENYLCHLOROFORMATE HAVING THE FORMULA,

WITH A METHYLAMINE DERIVATIVE HAVING THE FORMULA,
摘要翻译：可用作杀真菌剂的具有式（I）的氨基甲酸酯，其中R 1是卤素原子或硝基，低级烷基，低级烷氧基，低级烷硫基，氰基，磺酰胺，低级烷基亚磺酰基或低级烷基磺酰基，以及基团由R1m1表示可以相同或不同; m1为1〜5的整数， X是呋喃基或噻吩基或下式的基团，其中Y是氧或硫原子; R2是氢原子，卤素原子，烷基或烷氧基; m2为1〜5的整数; 并且n为0或1.该化合物是由I制备的。具有该配方的苯基氯化铵与具有该配方的甲基胺衍生物H 2 N-CH 2 -X ii反应。使具有下式的苯酚与具有式I的异氰酸酯衍生物，OCN-CH2-X或III反应。反应具有下式的苯基-N，N-亚乙基氨基甲酸酯：具有苯酚，噻吩酚或具有式的四氢呋喃，IV。用具有本发明公式的苯酚反应具有公式的碳酰氯，其中R1，R2，m1，m2，n，X和Y如上所定义。

6. 发明授权

US3899582A Aromatic imidocarbonate composition and method of use for combatting fungi 失效
标题翻译：芳香酰亚胺碳酸酯组合物和用于对抗真菌的方法
公开(公告)号：US3899582A
公开(公告)日：1975-08-12
申请号：US43842574
申请日：1974-01-31
申请人： SUMITOMO CHEMICAL CO
发明人： TANAKA SHIZUYA , OZAKI TOSHIAKI , MINE AKIHIKO , TANAKA KATSUTOSHI , YAMAMOTO SIGEO , OOISHI TADASHI , HINO NAGANORI , SATOMI TAKEO
IPC分类号： C07D213/74 , A01N9/22
CPC分类号： C07D213/74
摘要： Novel imidocarbonate derivatives having the formula:

wherein Y and Z, which may be the same or different, are individually an oxygen or sulfur atom; Ar is an unsubstituted or a halogen- or lower C1 - C4 alkyl (straight or branched)substituted benzene or pyridine nucleus, the number of the substituents being 1 to 3; R2 is a C1 - C18 alkyl (straight or branched), a C1 - C18 alkyl(straight or branched) having 1 to 3 hydroxy radicals or 1 to 3 alkoxycarbonyl (the alkoxy has 1 to 4 carbon atoms) radicals in the carbon chain, a C3 - C10 cycloalkyl, a C2 - C5 alkenyl (straight or branched), a C3 - C6 alkynyl (straight or branched), a phenylalkyl, the benzene nucleus of which may be unsubstituted or substituted by 1 to 4 halogen atoms, 1 to 4 lower C1 - C4 alkyl (straight or branched) radicals or a nitro radical, or a halogen- or lower C1 - C4 alkyl (straight or branched)-substituted phenoxyalkyl; R3 is a C1 - C18 alkyl (straight or branched) having 1 to 3 hydroxy radicals or 1 to 3 alkoxycarbonyl (the alkoxy has 1 to 4 carbon atoms) radicals in the carbon chain, a C2 - C5 alkenyl (straight or branched), a C3 - C6 alkynyl (straight or branched) or a phenylalkyl, the benzene nucleus of which may be unsubstituted or substituted by 1 to 4 halogen atoms, 1 to 4 lower C1 - C4 alkyl (straight or branched) radicals, a nitro radical or a C2 - C4 alkylene radical, provided that in case Ar is an unsubstituted or substituted benzene nucleus and R2 and R3 are phenylalkyl groups, the benzene nucleus of at least one of said phenylalkyl groups has a substituent, have strong microbicidal activities on a wide scope of microorganisms.
摘要翻译：具有下式的新型亚氨基碳酸酯衍生物：Y-R2 Ar-N = C ANGLE Z-R3其中Y和Z可以相同或不同，分别为氧或硫原子; Ar是未取代的或卤素 - 或低级C 1 -C 4烷基（直链或支链）取代的苯或吡啶核，取代基数为1至3; R2是碳链中具有1至3个羟基或1至3个烷氧基羰基（烷氧基具有1至4个碳原子）的C1-C18烷基（直链或支链），C1-C18烷基（直链或支链） C3-C10环烷基，C2-C5烯基（直链或支链），C3-C6炔基（直链或支链），苯基烷基，其苯核可以是未取代的或被1-4个卤素原子取代，1〜 4个低级C1-C4烷基（直链或支链）基或硝基，或卤素 - 或低级C1-C4烷基（直链或支链）取代的苯氧基烷基; R3是碳链中具有1至3个羟基或1至3个烷氧基羰基（烷氧基具有1至4个碳原子）基团的C1-C18烷基（直链或支链），C2-C5链烯基（直链或支链） C 3 -C 6炔基（直链或支链）或苯基烷基，其苯核可以是未取代的或被1至4个卤素原子取代，1至4个低级C 1 -C 4烷基（直链或支链）基团，硝基或如果Ar是未取代或取代的苯核，且R 2和R 3为苯基烷基，则所述苯基烷基中的至少一个的苯核具有取代基，在宽范围内具有强的杀微生物活性的微生物。

7. 发明授权

US3670057A S(alkllthio ethyl) phosphorothioamidate 失效
标题翻译： S（ALKLLTHIO ETHYL）磷酸生物酰胺
公开(公告)号：US3670057A
公开(公告)日：1972-06-13
申请号：US3670057D
申请日：1969-11-10
申请人： SUMITOMO CHEMICAL CO
发明人： TSUCHIYA HIROSHI , MUKAI KUNIO , KIMURA AKIO , KAWANO SUMINORI , FUJIMOTO KEIMEI , OZAKI TOSHIAKI , YAMAMOTO SIGEO , OKUNO YOSITOSI , TANAKA KATSUTOSHI , TAKEDA HISAMI , OOISHI TADASHI
IPC分类号： C07F9/24 , A01N9/36
CPC分类号： C07F9/2408
摘要： A phosphorothioamidate having the formula, WHEREIN R1 is an alkyl having up to four carbon atoms, R2 and R3 are individually a hydrogen atom, an alkyl having up to 10 carbon atoms, a cycloalkyl having up to 6 carbon atoms, a phenyl, an aralkyl having up to eight carbon atoms or an alkenyl having up to five carbon atoms, R4 and R5 are each alkyl having up to five carbon atoms, and X is an oxygen or sulfur atom, which may be effectively used as an insecticidal, acaricidal and fungicidal composition. The phosphorothioamidate is prepared by (1) dealkylating a thionophosphoric acid amidate having the formula, WHEREIN R1, R2 and R3 are as defined above, with an alkali hydrosulfide, to prepare a phosphate having the formula, (2) CONDENSING THE THUS OBTAINED PHOSPHATE WITH A HALOGEN COMPOUND HAVING THE FORMULA, WHEREIN Hal represents a halogen atom, and R4, R5 and X are as defined above.
摘要翻译：具有下式的硫代酰胺酸盐，其中R1是具有至多4个碳原子的烷基，R2和R3分别是氢原子，具有至多10个碳原子的烷基，具有至多6个碳原子的环烷基，苯基，芳烷基具有多达8个碳原子或具有至多5个碳原子的烯基，R 4和R 5各自是具有至多5个碳原子的烷基，X是氧或硫原子，其可有效地用作杀虫，杀螨和杀真菌剂组成。

8. 发明授权

US3745170A Novel n-(3,5-dihalophenyl)-imide compounds 失效
标题翻译：新型N-（3,5-二羟基苯基） - 化合物
公开(公告)号：US3745170A
公开(公告)日：1973-07-10
申请号：US1733970
申请日：1970-03-06
申请人： SUMITOMO CHEMICAL CO
发明人： FUJINAMI AKIRA , OZAKI TOSHIAKI , KAMEDA NOBUYUKI , AKIBA KEIICHIRO , OOISHI TADASHI , NODERA KATSUJI , TANAKA KATSUTOSHI , OOBA SHIGEHIRO , YAMAMOTO SIGEO
IPC分类号： C07D207/40 , C07D207/404 , C07D207/44 , C07D207/452 , C07D209/48 , C07D209/52 , C07D211/88 , C07D295/15 , C07D29/10
CPC分类号： C07D207/408 , C07D207/40 , C07D207/44 , C07D207/452 , C07D209/48 , C07D209/52 , C07D211/88 , C07D295/15 , Y10S514/949
摘要： NOVEL N-(3,5-DIHOLOPHENYL)IMIDE COMPOUNDS, WHICH EXHIBIT A STRONG ANTIMICROBIAL ACTIVITY AGAINST MICROORGANISMS INCLUDING PHYTOPATHOGENIC FUNGI, PARASITES OF INDUSTRIAL PRODUCTS AND PATHOGENIC MICROORGANISMS, REPRESENTED BY THE FORMULA,

(3-X,5-X''-PHENYL)-N
WHEREIN X AND X'' EACH REPRESENT HALOGENS AND A REPRESENTS A SUBSTITUTED ETHYLENE SUCH AS CHLOROETHYLENE, C1C4 ALKYLTHIOETHYLENE, C1-C2 ALKYL-ETHYLENE OR 1,2-DI-C1C2-ALKYL-ETHYLENE, A CYCLOPROPYLENE SUCH AS 1,3-DIMETHYLCYCLOPROPYLENE, TRIMETHYLENE, A CYCLOHEXYLENE-1,2-, CYCLOHEXENYLENE-1,2-, CYCLOHEXADIENYLENE-1,2- OR O-PHENYLENE. THE N-(3,5-DIHALOPHENY)IMIDE COMPOUNDS CAN BE OBTAINED BY ANY OF METHODS WHICH PRODUCE IMIDE COMPOUNDS ON REACTION OF AN N-(3,5-DIHALOPHENYL)MALEIMIDE COMPOUND WITH A MERCAPTAN, A HYDROGEN HALIDE, PHOSPHORUS CHLORIDE OR THIONYLCHLORIDE.

9. 发明授权

US3668217A 3-(3{40 ,5{40 -dihalogenophenyl)imidazolidine-2,4-dione derivatives 失效
标题翻译： 3-（3 {40,5 {40-二氢壬基）咪唑烷-2,4-二酮衍生物
公开(公告)号：US3668217A
公开(公告)日：1972-06-06
申请号：US3668217D
申请日：1969-11-14
申请人： SUMITOMO CHEMICAL CO
发明人： FUJINAMI AKIRA , OZAKI TOSHIAKI , HORIUCHI FUKASHI , YAMAMOTO SIGEO , AKIBA KELICHIRO , TANAKA KATSUTOSHI , OOBA SHIGEHIRO , OOISHI TADASHI , NODERA KATSUJI , KAMEDA NOBUYUKI
IPC分类号： C07D233/72 , C07D233/74 , C07D233/76
CPC分类号： C07D233/72 , C07D233/76
摘要： 3-(3'',5''-Dihalogenophenyl)imidazolidine-2,4-dione derivatives, which may be substituted with alkyl or phenyl in the 1 and/or 5 positions, are new compounds, and have high microbicidal activity on various fungi and bacteria and are non-toxic to plants and mammals. Those compounds are prepared by the intramolecular cyclization of a corresponding urea derivatives.
摘要翻译：在1和/或5个位置可被烷基或苯基取代的3-（3'，5'-二卤代苯基）咪唑烷-2,4-二酮衍生物是新化合物，对各种真菌具有高杀微生物活性，细菌，对植物和哺乳动物无毒。这些化合物通过相应的脲衍生物的分子内环化制备。

10. 发明授权

US3903090A Novel n-(3,5-dihalophenyl)-imide compounds 失效
标题翻译：新型n-（3,5-二卤苯基） - 酰亚胺化合物
公开(公告)号：US3903090A
公开(公告)日：1975-09-02
申请号：US32216973
申请日：1973-01-09
申请人： SUMITOMO CHEMICAL CO
发明人： FUJINAMI AKIRA , OZAKI TOSHIAKI , OOBA SHIGEHIRO , YAMAMOTO SIGEO , NODERA KATSUJI , TANAKA KATSUTOSHI , AKIBA KEIICHIRO , OOISHI TADASHI , KAMEDA NOBUYUKI
IPC分类号： C07D207/40 , C07D207/404 , C07D207/44 , C07D207/452 , C07D209/48 , C07D209/52 , C07D211/88 , C07D295/15 , C07D39/00
CPC分类号： C07D207/408 , C07D207/40 , C07D207/44 , C07D207/452 , C07D209/48 , C07D209/52 , C07D211/88 , C07D295/15
摘要： Novel N-(3,5-dihalophenyl)imide compounds, which exhibit a strong antimicrobial activity against microorganisms including phytopathogenic fungi, parasites of industrial products and pathogenic microorganisms, represented by the formula,

wherein X and X'' each represent halogens and A represents a substituted ethylene such as chloroethylene, C1-C4 alkylthioethylene, C1-C2 alkyl-ethylene or 1,2-di-C1-C2-alkylethylene, a cyclopropylene such as 1,3-dimethylcyclopropylene, trimethylene, a cyclohexylene-1,2-, cyclohexenylene-1,2-, cyclohexadienylene-1,2- or o-phenylene. The N-(3,5-dihalophenyl)imide compounds can be obtained by any of methods which produce imide compounds or reaction of an N(3,5-dihalophenyl)maleimide compound with a mercaptan, a hydrogen halide, phosphorus chloride or thionylchloride.
摘要翻译：新型N-（3,5-二卤代苯基）酰亚胺化合物，其表现出对微生物的强烈抗微生物活性，包括植物病原性真菌，工业产品寄生虫和致病微生物，由下式表示：O | CN ANGLE ANGLE AC | O其中X和X “各自表示卤素，A表示取代的乙烯，例如氯乙烯，C 1 -C 4烷基硫代乙烯，C 1 -C 2烷基 - 乙烯或1,2-二-C 1 -C 2烷基 - 乙烯，亚环烷基如1,3-二甲基亚丙基，亚环己基-1,2-亚环己基-1,2-环己二烯-1,2-或邻亚苯基。

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