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1. 发明授权

US06300323B1 (Poly)ethereal ammonium salts of herbicides bearing acidic moieties and their use as herbicides 有权
标题翻译：（Poly）具有酸性部分的除草剂醚醚铵盐及其作为除草剂的用途
公开(公告)号：US06300323B1
公开(公告)日：2001-10-09
申请号：US09634630
申请日：2000-08-08
申请人： Takahiro Haga , Kevin E. Crosby , Jeffrey R. Schussler
发明人： Takahiro Haga , Kevin E. Crosby , Jeffrey R. Schussler
IPC分类号： A01N5712
CPC分类号： C07D213/64 , A01N25/30 , A01N33/08 , A01N39/02 , A01N39/04 , A01N43/40 , A01N43/54 , A01N43/56 , A01N43/84 , A01N57/20 , C07C215/08 , C07C215/14 , C07C215/18 , C07C217/08 , C07C217/16 , C07C217/28 , C07C217/42 , C07C219/04 , C07C219/08 , C07D213/80 , C07D231/20 , C07D239/34 , C07D295/088 , C07F9/3813 , C08G65/33306
摘要： A compound Wherein x, y, and z are integers from 0 to 3; and the (poly)ethereal amine is at least one selected from compounds of formula II1 through II5:
摘要翻译：复合物，其中x，y和z是0至3的整数; 和（多）醚胺是选自式II1至II5的化合物中的至少一种：

2. 发明授权

US06455469B1 Herbicidal composition 失效
标题翻译：除草成分
公开(公告)号：US06455469B1
公开(公告)日：2002-09-24
申请号：US09729233
申请日：2000-12-05
申请人： Kevin E. Crosby , Jeffrey R. Schussler , Takahiro Haga
发明人： Kevin E. Crosby , Jeffrey R. Schussler , Takahiro Haga
IPC分类号： A01N3734
CPC分类号： A01N37/22 , A01N37/34 , A01N43/10 , A01N43/80 , A01N43/70 , A01N43/54 , A01N2300/00
摘要： The present invention provides to a herbicidal composition comprising as the effective components A) at least one substituted acetanilide derivative of the formula I: □EMBED ChemDraw.Document.4.5 □□□ wherein n is an integer of 1 or 2 R is H, halogen, C1-4 alkyl or C1-2 alkoxy Q is cyanomethyl or propargyl X is halogen B) at least one compound selected from the group consisting of aryloxyalkanoic acids, aromatic carboxylic acids, ureas, triazines, anilides, hydroxybenzonitriles, quaternary ammonium salts, triketones, aryloxyphenoxypropionic acids, oximes, sulfonylureas, imidazolinones, dinitroanilines, chloroacetanilides, oxyacetamides, thiocarbamates, amides, semicarbazones, amino acids, and inhibitors of protoporphyrinogen oxidase that includes diphenyl ethers, substituted uracils, pyrazoles, triazolinones and triazolopyridinones.
摘要翻译：本发明提供了一种除草组合物，其包含作为有效成分的A）至少一种式I的取代的乙酰苯胺衍生物：其中n为1或2R的整数为H，卤素，C 1-4烷基或C 1-2烷氧基Q为氰基甲基或炔丙基X为卤素B）至少一种选自芳氧基烷酸，芳族羧酸，脲，三嗪，苯胺，羟基苯腈，季铵盐，三酮，芳氧基苯氧基丙酸，肟，磺酰脲，咪唑啉酮，二硝基苯胺，氯乙酰苯胺，氧乙酰胺氨基甲酸酯，酰胺，缩氨基脲，氨基酸和原卟啉原氧化酶的抑制剂，其包括二苯醚，取代的尿嘧啶，吡唑，三唑啉酮和三唑并吡啶酮。

3. 发明授权

US06303543B1 Diaryl ethers and processes for their preparation and herbicidal and desiccant compositions containing them 失效
标题翻译：二芳基醚及其制备方法和含有它们的除草和干燥剂组合物
公开(公告)号：US06303543B1
公开(公告)日：2001-10-16
申请号：US09570911
申请日：2000-05-15
申请人： David A. Pulman , Bai-Ping Ying , Shao-Yong Wu , Sandeep Gupta , Masamitsu Tsukamoto , Takahiro Haga
发明人： David A. Pulman , Bai-Ping Ying , Shao-Yong Wu , Sandeep Gupta , Masamitsu Tsukamoto , Takahiro Haga
IPC分类号： C07D23156
CPC分类号： C07D231/20 , A01N43/50 , A01N43/52 , A01N43/54 , A01N43/56 , A01N43/58 , A01N43/60 , A01N43/653 , A01N43/66 , A01N43/713 , A01N43/76 , A01N43/80 , A01N43/90 , C07D231/18 , A01N2300/00 , A01N47/36 , A01N47/06 , A01N43/10 , A01N37/22
摘要： A compound represented by the formula (I) or its salt and herbicidal and desiccant use thereof: wherein X, Y are independently hydrogen, halogen, cyano, nito, or (C1-6)haloalkyl; Z is oxygen or sulfur; and
摘要翻译：由式（I）表示的化合物或其盐和除草和干燥剂的用途：其中X，Y独立地是氢，卤素，氰基，硝基或（C 1-6）卤代烷基; Z是氧或硫; 和

4. 发明授权

US5855692A Battery charger and solar cells for battery charging 失效
标题翻译：电池充电器和太阳能电池用于电池充电
公开(公告)号：US5855692A
公开(公告)日：1999-01-05
申请号：US904614
申请日：1997-08-01
申请人： Masanori Kaji , Masayosi Ono , Yosinobu Takabatake , Yosinori Kaido , Takahiro Haga , Masaru Hikosaka
发明人： Masanori Kaji , Masayosi Ono , Yosinobu Takabatake , Yosinori Kaido , Takahiro Haga , Masaru Hikosaka
IPC分类号： A45C15/00 , E05D11/00 , H01L31/045 , H01L31/058 , H01R4/48 , H02J7/00 , H02J7/35 , H01L25/00 , H01M10/44
CPC分类号： H02J7/355 , A45C15/00 , H01R4/48 , H02J7/0042 , H02S10/40 , H02S30/20 , H02S40/38 , E05D11/0081 , E05Y2900/606 , Y10S136/293
摘要： A battery charger is provided with a battery charger unit which connects to, and charges a battery Solar cells are used as the source of power for charging the battery, and connecting parts electrically connect the solar cells and the battery charger unit. The battery charger unit is provided with a solar cell compartment for stowing the solar cells batteries when not in use charging a battery.
摘要翻译：电池充电器设置有连接到电池和对电池充电的电池充电器单元。太阳能电池被用作为电池充电的电源，并且连接部件电连接太阳能电池和电池充电器单元。电池充电器单元设置有太阳能电池室，用于在不使用电池时对太阳能电池电池进行充电。

5. 发明授权

US5492908A Diaminotrifluoromethylpyridine derivatives, process for their production and phospholipase A.sub.2 inhibitor containing them 失效
标题翻译：二氨基三氟甲基吡啶衍生物，其制备方法和含有它们的磷脂酶A2抑制剂
公开(公告)号：US5492908A
公开(公告)日：1996-02-20
申请号：US285271
申请日：1994-08-03
申请人： Takahiro Haga , Hideo Sugi , Itaru Shigehara , Shinji Odawara , Syuichi Yotsuya , Hirohiko Kimura , Kazuhiro Yamamoto
发明人： Takahiro Haga , Hideo Sugi , Itaru Shigehara , Shinji Odawara , Syuichi Yotsuya , Hirohiko Kimura , Kazuhiro Yamamoto
IPC分类号： A61K31/4427 , A61P5/48 , A61P29/00 , C07D213/75 , C07D213/76 , C07D401/12 , C07D405/12 , C07D409/12 , C07D413/12 , C07D417/12 , C07D453/02 , C07D495/04 , A61K31/44 , A61K31/495 , A61K31/54
CPC分类号： C07D213/75 , C07D213/76 , C07D401/12 , C07D405/12 , C07D409/12 , C07D413/10 , C07D413/12 , C07D417/12 , C07D453/02 , C07D495/04
摘要： A method of treating rheumatoid arthritis using a diaminotrifluoromethylpyridine derivative of the formula (I) or its salt: ##STR1## wherein X is --CW.sup.1 R.sup.1, --COCOR.sup.2, --CW.sup.1 NHCOR.sup.2, --C(.dbd.W.sup.1)W.sup.2 R.sup.3 or --CW.sup.1 N(R.sup.4)R.sup.5, and Y is alkyl, --CW.sup.3 R.sup.6, --COCOR.sup.7, --NHCOR.sup.7, --C(.dbd.W.sup.3)W.sup.4 R.sup.8, --(NH).sub.m SO.sub.2 R.sup.9, --(NH).sub.m SO.sub.2 OR.sup.10 or --(NH).sub.m SO.sub.2 N(R.sup.11)R.sup.12, wherein each of R.sup.1, R.sup.6 and R.sup.9, which are independent from one another, is a chain hydrocarbon group which may be substituted, a monocyclic hydrocarbon group which may be substituted, a polycyclic hydrocarbon group which may be substituted, a monocyclic heterocycle group which may be substituted or a polycyclic heterocycle group which may be substituted as further defined herein.
摘要翻译：一种使用式（I）的二氨基三氟甲基吡啶衍生物或其盐进行类风湿性关节炎的方法：其中X为-CW1R1，-COCOR2，-CW1NHCOR2，-C（= W1）W2R3或-CW1N（R4 ）R5，Y是烷基，-CW3R6，-COCOR7，-NHCOR7，-C（= W3）W4R8， - （NH）mSO2R9， - （NH）mSO2OR10或 - （NH）mSO2N（R11）R12， R 1，R 6和R 9彼此独立地是可以被取代的链状烃基，可以被取代的单环烃基，可以被取代的多环烃基，可被取代的单环杂环基或可以如本文进一步定义的可被取代的多环杂环基团。

6. 发明授权

US5168113A Mercapto-substituted pyridine compounds 失效
标题翻译：巯基取代的吡啶化合物
公开(公告)号：US5168113A
公开(公告)日：1992-12-01
申请号：US471337
申请日：1990-01-29
申请人： Takahiro Haga , Yasuhiro Tsujii , Tatsuo Isogai , Shigeo Murai , Hisayoshi Jonishi , Tokiya Kimura , Hiroshi Sasaki , Takao Awazu , Toshihiro Tanaka
发明人： Takahiro Haga , Yasuhiro Tsujii , Tatsuo Isogai , Shigeo Murai , Hisayoshi Jonishi , Tokiya Kimura , Hiroshi Sasaki , Takao Awazu , Toshihiro Tanaka
IPC分类号： A01N43/40 , C07D213/82 , C07D213/89 , C07D401/12
CPC分类号： C07D213/82 , A01N43/40 , C07D213/89 , C07D401/12
摘要： A mercapto-substituted pyridine compound having formula (I): ##STR1## where R.sub.1 and R.sub.2 are alkyl groups, and n is 0 or 1, and salts thereof and a process for preparing the same are disclosed. The mercapto-substituted pyridine compound is useful as an intermediate for preparing a herbicidal compound.The present invention further provides aminocarbonyl-substituted pyridinesulfinic acid (ACPS) or salts thereof as the precursor of aminosulfonyl-substituted pyridinecarbonic acid amide compound (APCA) which is useful as the starting material for agricultural chemicals, medicine, etc. Moreover, the preparation process of the present invention is an industrially advantageous preparation process which is capable of preparing in a series of steps from mercapto-substituted pyridinecarboxylic acid amide compound (MPCA) or aminocarbonyl-substituted halogenopyridine compound (ACHP) to ACPS or salts thereof, and further to APCA.
摘要翻译：公开了具有式（I）的巯基取代的吡啶化合物：其中R 1和R 2是烷基，n是0或1，及其盐及其制备方法。巯基取代的吡啶化合物可用作制备除草化合物的中间体。本发明还提供氨基羰基取代的吡啶亚磺酸（ACPS）或其盐作为氨基磺酰基取代的吡啶碳酰胺化合物（APCA）的前体，其可用作农药，药物等的原料。此外，制备方法本发明是一种工业上有利的制备方法，其能够从巯基取代的吡啶羧酸酰胺化合物（MPCA）或氨基羰基取代的卤代吡啶化合物（ACHP）到ACPS或其盐，以及APCA 。

7. 发明授权

US5128474A Mercapto-substituted pyridine compounds, aminocarbonyl-substituted pyridinesulfinic acid compounds and process for preparing the same 失效
标题翻译：巯基取代的吡啶化合物，氨基羰基取代的吡啶亚磺酸化合物及其制备方法
公开(公告)号：US5128474A
公开(公告)日：1992-07-07
申请号：US558545
申请日：1990-07-27
申请人： Takahiro Haga , Yasuhiro Tsujii , Tatsuo Isogai , Shigeo Murai , Hisayoshi Jonishi , Tokiya Kimura , Hiroshi Sasaki , Takao Awazu , Toshihiro Tanaka
发明人： Takahiro Haga , Yasuhiro Tsujii , Tatsuo Isogai , Shigeo Murai , Hisayoshi Jonishi , Tokiya Kimura , Hiroshi Sasaki , Takao Awazu , Toshihiro Tanaka
IPC分类号： A01N43/40 , C07D213/82 , C07D213/89 , C07D401/12
CPC分类号： C07D213/82 , A01N43/40 , C07D213/89 , C07D401/12
摘要： An aminocarbonyl-substituted pyridinesulfinic acid intermediate for production of an herbicide having formula (V): ##STR1## wherein R.sub.3 and R.sub.4 are selected from the group consisting of hydrogen and alkyl groups, or a salt thereof. The aminocarbonyl-substituted pyridinesulfinic acid or salt thereof is useful as the precursor of aminosulfonyl-substituted pyridinecarbonic acid amide, which in turn is useful as the starting material for agricultural chemicals, medicine, etc.
摘要翻译：用于制备具有式（V）的除草剂的氨基羰基取代的吡啶亚磺酸中间体：其中R 3和R 4选自氢和烷基，或其盐。氨基羰基取代的吡啶亚磺酸或其盐可用作氨基磺酰基取代的吡啶碳酰胺的前体，其又可用作农药，药物等的起始原料。

8. 发明授权

US5116949A Benzoyl urea compound-albumin complex 失效
标题翻译：苯甲酸脲化合物 - 铝复合物
公开(公告)号：US5116949A
公开(公告)日：1992-05-26
申请号：US400941
申请日：1989-08-31
申请人： Tsunetaka Nakajima , Tadao Okamoto , Nobuo Kondo , Masahiro Watanabe , Koichi Yamauchi , Kazumasa Yokoyama , Takahiro Haga , Nobutoshi Yamada , Hideo Sugi , Toru Koyanagi
发明人： Tsunetaka Nakajima , Tadao Okamoto , Nobuo Kondo , Masahiro Watanabe , Koichi Yamauchi , Kazumasa Yokoyama , Takahiro Haga , Nobutoshi Yamada , Hideo Sugi , Toru Koyanagi
IPC分类号： A61K31/44 , A61K31/4418 , A61K31/505 , A61K38/16 , A61K47/48 , A61P35/00 , C07D213/64 , C07D213/647 , C07D239/34 , C07K14/00 , C07K14/435 , C07K14/76
CPC分类号： C07D213/647 , A61K31/44 , A61K31/505 , A61K47/48284 , C07D239/34
摘要： A benzoyl urea compound-albumin complex comprising a benzoyl urea compound of the formula: ##STR1## wherein X is a halogen atom or a nitro group, Y is a hydrogen atom, a halogen atom, a nitro group or a trifluoromethyl group, Z.sub.1 is a halogen atom or a trifluoromethyl group, Z.sub.2 is a hydrogen atom or a halogen atom and A is CH or a nitrogen atom, and albumin.

9. 发明授权

US5002952A Readily absorbed pharmaceutical composition 失效
标题翻译：容易吸收药物成分
公开(公告)号：US5002952A
公开(公告)日：1991-03-26
申请号：US385998
申请日：1989-07-27
申请人： Nobuo Kondo , Tsunetaka Nakajima , Masahiro Watanabe , Kazumasa Yokoyama , Takahiro Haga , Nobutoshi Yamada , Hideo Sugi , Toru Koyanagi
发明人： Nobuo Kondo , Tsunetaka Nakajima , Masahiro Watanabe , Kazumasa Yokoyama , Takahiro Haga , Nobutoshi Yamada , Hideo Sugi , Toru Koyanagi
IPC分类号： A61K47/44 , A61K9/14 , A61K31/44 , A61K31/505 , A61K47/06 , A61P35/00 , C07D213/64
CPC分类号： A61K9/145 , A61K31/44 , A61K31/505 , Y10S514/941 , Y10S514/975
摘要： A pharmaceutical composition comprising a benzoyl urea compound having the formula: ##STR1## wherein X is a halogen atom or a nitro group, Y is a hydrogen atom, a halogen atom, a nitro group or a trifluoromethyl group, Z.sub.1 is a halogen atom or a trifluoromethyl group, Z.sub.2 is a hydrogen atom or a halogen atom, and A is a .dbd.CH--group or a nitrogen atom, and a nonionic surfactant.
摘要翻译：一种药物组合物，其包含具有下式的苯甲酰脲化合物：其中X为卤素原子或硝基，Y为氢原子，卤素原子，硝基或三氟甲基，Z1为卤素原子或三氟甲基，Z 2为氢原子或卤素原子，A为= CH-基或氮原子，和非离子表面活性剂。

10. 发明授权

US4929729A Process for producing 2-amino-4,6-dichloropyrimidine 失效
标题翻译： 2-氨基-4,6-二氯嘧啶的制备方法
公开(公告)号：US4929729A
公开(公告)日：1990-05-29
申请号：US304031
申请日：1989-01-31
申请人： Takahiro Haga , Yasuhiro Tsujii , Tatsuo Isogai , Shigeo Murai , Toshihiro Tanaka
发明人： Takahiro Haga , Yasuhiro Tsujii , Tatsuo Isogai , Shigeo Murai , Toshihiro Tanaka
IPC分类号： C07D239/42
CPC分类号： C07D239/42
摘要： The present invention relates to an industrially advantageous process for producing 2-amino-4,6-dichloropyrimidine, which comprises reacting 2-amino-4,6-dihydroxypyrimidine or its salt with phosphorus oxychloride at a temperature of from 50.degree. to 100.degree. C. in the presence of a solvent and an acid removing agent. Further, the yield of 2-amino-4,6-dichloropyrimidine can be improved by hydrolyzing 4,6-dichloro-2-pyrimidinylphosphoramidic dichloride produced as a by-product of the chlorination reaction to form 2-amino-4,6-dichloropyrimidine. The 2-amino-4,6-dichloropyrimidine produced by the process of the present invention is useful as an intermediate for medicines and agricultural chemicals.

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