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11. 发明授权

US06982344B2 Process for preparation of optically active sulfonamides and intermediates for their synthesis 有权
标题翻译：制备光学活性磺酰胺及其合成中间体的方法
公开(公告)号：US06982344B2
公开(公告)日：2006-01-03
申请号：US10399165
申请日：2001-10-17
申请人： Tomomi Ikemoto , Atsuko Nishiguchi , Kiminori Tomimatsu
发明人： Tomomi Ikemoto , Atsuko Nishiguchi , Kiminori Tomimatsu
IPC分类号： C07C311/51 , C07C311/14 , C07C311/28 , C07C303/40 , C07B57/00
CPC分类号： C07C311/51 , C07B2200/07 , C07C303/40 , C07C303/44 , C07C311/14 , C07C2601/16
摘要： A method including resolution of a diastereomeric mixture represented by the formula wherein R1 and R2 are the same or different and each is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, only one of R1 and R2 contains one asymmetric carbon, and Ra is an optically active and optionally substituted hydrocarbon group or an optically active and optionally substituted heterocyclic group, or a salt thereof, to produce the diastereomer having a steric configuration of the asymmetric carbon for R1 or R2 of an R configuration or an S configuration, or a salt thereof.
摘要翻译：一种包括由下式表示的非对映异构体混合物的拆分方法，其中R 1和R 2相同或不同，并且各自为任选取代的烃基或任选取代的杂环基团中，R 1和R 2中只有一个含有一个不对称碳，R a是光学活性和任选取代的烃基或光学活性和任选取代的杂环基或其盐，以产生R构型的R 1或R 2的不对称碳的立体构型的非对映异构体或 S构型或其盐。

12. 发明申请

US20050107606A1 Process for producing optically active sulfoxide derivative 审中-公开
标题翻译：光学活性亚砜衍生物的制备方法
公开(公告)号：US20050107606A1
公开(公告)日：2005-05-19
申请号：US10506955
申请日：2003-03-11
申请人： Hiroyuki Tawada , Tomomi Ikemoto , Atsuko Nishiguchi , Tatsuya Ito , Mari Adachi
发明人： Hiroyuki Tawada , Tomomi Ikemoto , Atsuko Nishiguchi , Tatsuya Ito , Mari Adachi
IPC分类号： C07D233/64 , A61K31/4164 , A61K31/55 , A61P43/00 , C07D225/06 , C07D233/54 , C07D403/12 , C07D43/02
CPC分类号： C07D233/64 , C07D225/06 , C07D403/12 , Y02P20/582
摘要： A process for preparing an optically active sulfoxide derivative (I) having CCR5 antagonism without causing side reactions such as racemization and Pummerer rearrangement, which comprises reacting a compound (II) with a compound (III) as shown by the following scheme: wherein R1 represents hydrogen, an aliphatic hydrocarbon group or an aromatic group; R2 represents halogeno, alkyl, hydroxyl, amino, an aromatic group, etc.; R3 represents a 5- or 6-membered ring; R4 represents hydrogen, alkyl, alkoxy or halogeno; R5 represents hydrogen, a hydrocarbon group, a heterocyclic group, acyl, etc.; ring A represents an optionally substituted benzene ring; X represents a bond or divalent group comprising a linear part constituted of 1 to 4 atoms; m represents an integer of 1 to 5; n represents an integer of 0 to 3; p represents an integer of 0 to 2; and *1 represents an asymmetric center.
摘要翻译：一种制备具有CCR5拮抗作用的光学活性亚砜衍生物（I）的方法，不会引起副反应，例如外消旋化和Pummerer重排，其包括使化合物（II）与化合物（III）反应，如下列方案所示：其中R SUP> 1表示氢，脂族烃基或芳基; R 2表示卤代，烷基，羟基，氨基，芳基等; R 3表示5或6元环; R 4表示氢，烷基，烷氧基或卤代; R 5表示氢，烃基，杂环基，酰基等; 环A表示任选取代的苯环; X表示包含由1至4个原子构成的直链部分的键或二价基团; m表示1〜5的整数， n表示0〜3的整数， p表示0〜2的整数，和* 1 表示不对称中心。

13. 发明授权

US06743924B2 Method for producing 1-substituted-1,2,3-triazole derivative 失效
标题翻译： 1-取代-1,2,3-三唑衍生物的制备方法
公开(公告)号：US06743924B2
公开(公告)日：2004-06-01
申请号：US10019264
申请日：2002-04-19
申请人： Tomomi Ikemoto , Tatsuya Ito , Kiminori Tomimatsu , Yasuhiro Sawai , Hirohiko Nishiyama , Yasushi Isogami
发明人： Tomomi Ikemoto , Tatsuya Ito , Kiminori Tomimatsu , Yasuhiro Sawai , Hirohiko Nishiyama , Yasushi Isogami
IPC分类号： C07D24904
CPC分类号： C07D249/04
摘要： A method for producing a compound of the formula: (1) in a secondary or tertiary alcohol in the presence of a base, or (2) in the absence of a base is provided. According to this method, a 1-substituted-1,2,3-triazole compound having a tyrosine kinase inhibitory action can be produced efficiently in a high yield at an industrial large scale by a convenient method
摘要翻译：制备下式化合物的方法：（1）在仲醇或叔醇中，在碱的存在下，或（2）在不存在碱的情况下。根据该方法，可以通过方便的方法以工业大规模高效率地产生具有酪氨酸激酶抑制作用的1-取代-1,2,3-三唑化合物

14. 发明授权

US07521545B2 Azo compounds and process for production thereof 失效
标题翻译：偶氮化合物及其制备方法
公开(公告)号：US07521545B2
公开(公告)日：2009-04-21
申请号：US11661183
申请日：2005-08-25
申请人： Tomomi Ikemoto , Takeshi Yamasaki
发明人： Tomomi Ikemoto , Takeshi Yamasaki
IPC分类号： C07D307/79 , C07D405/04
CPC分类号： C07D307/79 , C07D307/81 , C07D405/04
摘要： A process for the production of an aromatic azo compound having a 2,3-dihydrobenzofuran ring bearing a diazo group at the 5-position of the ring by conducting the diazo coupling of a 2,3-dihydrobenzofuran derivative represented by the general formula (II): [wherein R1 and R2 are each independently C1-6 alkyl; R3 is optionally substituted aryl; and R4, R5 and R6 are each independently hydrogen, C1-6 alkyl, halogeno, C1-6 alkoxy, or C1-6 alkylthio] with a benzenediazonium salt having an electron-withdrawing group at the p- and/or o-position in a mixed solvent composed of water and a polar organic solvent.
摘要翻译：通过进行由通式（II）表示的2,3-二氢苯并呋喃衍生物的重氮偶联，制备具有环的5-位上具有重氮基的2,3-二氢苯并呋喃环的芳族偶氮化合物的方法）：[其中R 1和R 2各自独立地为C 1-6烷基; R3是任选取代的芳基; 和R 4，R 5和R 6各自独立地为氢，C 1-6烷基，卤代，C 1-6烷氧基或C 1-6烷硫基]，其中在苯二氮基和/或位置上具有吸电子基团的苯二氮鎓盐由水和极性有机溶剂组成的混合溶剂。

15. 发明申请

US20070099986A1 Preventives/remedies for urinary disturbance 审中-公开
标题翻译：预防/治疗尿路障碍
公开(公告)号：US20070099986A1
公开(公告)日：2007-05-03
申请号：US11589903
申请日：2006-10-31
申请人： Yuji Ishichi , Koichi Iwanaga , Tomomi Ikemoto , Hiroaki Yamamoto , Shokyo Miki
发明人： Yuji Ishichi , Koichi Iwanaga , Tomomi Ikemoto , Hiroaki Yamamoto , Shokyo Miki
IPC分类号： A61K31/343 , A61K31/36 , C07D319/14 , A61K31/18 , C07C311/18
CPC分类号： C07C311/37 , C07C45/46 , C07C49/813 , C07C2602/08 , C07D307/79 , C07D319/18 , C07D405/04
摘要： A compound represented by the formula: wherein Ar represents a group represented by the formula: (wherein Y represents methylene or an oxygen atom, R1 represents aminosulfonyl, C1-6 alkylaminosulfonyl, C1-6 alkylcarbonylamino or C1-6 alkylsulfonylamino, R2 represents a hydrogen atom or C1-6 alkyl, R3 represents C1-6 alkyl, and R4 represents a hydrogen atom or C1-6 alkyl); X represents a carbonyl group, or a methylene group which may be substituted with a hydroxy group; and L represents an optionally substituted C4-5 alkylene group, or a salt thereof is provided.
摘要翻译：由下式表示的化合物：其中Ar表示由下式表示的基团：其中Y表示亚甲基或氧原子，R 1表示氨基磺酰基，C 1-6烷基，烷基氨基磺酰基，C 1-6烷基羰基氨基或C 1-6烷基磺酰基氨基，R 2表示氢原子或C 1-6 - / SUB烷基，R 3表示C 1-6烷基，R 4表示氢原子或C 1-6 烷基）; X表示羰基或可被羟基取代的亚甲基; L表示任意取代的C 4〜5亚烷基，或其盐。

16. 发明授权

US07038042B2 Process for producing cyclic compound 失效
标题翻译：环状化合物的制备方法
公开(公告)号：US07038042B2
公开(公告)日：2006-05-02
申请号：US11010215
申请日：2004-12-10
申请人： Tomomi Ikemoto , Tatsuya Ito , Kiminori Tomimatsu
发明人： Tomomi Ikemoto , Tatsuya Ito , Kiminori Tomimatsu
IPC分类号： C07D487/00 , C07C313/00
CPC分类号： C07D225/06 , C07D313/08 , C07D313/20
摘要： A process suitable for safely mass-producing, through a short step, cyclic compounds useful in medicines, agricultural chemicals, foods, cosmetics, and chemical products or as intermediates therefor. The process, which is for producing a compound represented by the formula: {wherein Z represents an electron-attracting group; W represents optionally substituted ethylene or optionally substituted vinylene; R3 represents hydrogen or an optionally substituted hydrocarbon group; and X represents a divalent group [provided that when W represents optionally substituted vinylene, then —X—CH2-Z is not —X1—X2—CH2, -Z (wherein X1 represents sulfur or optionally substituted nitrogen and X2 represents optionally substituted ethylene)]} or a salt thereof, is characterized by subjecting a compound represented by the formula (II) or a salt thereof: (wherein the symbols have the same meanings as the above) to a ring closure reaction in a solvent containing a carbonic diester.
摘要翻译：一种适用于通过短步安全批量生产用于药物，农药，食品，化妆品和化学产品的环状化合物或其中间体的方法。该方法用于制备由下式表示的化合物：其中Z表示吸电子基团; W表示任选取代的乙烯或任选取代的亚乙烯基; R 3表示氢或任选取代的烃基; 并且X表示二价基团[条件是当W表示任选取代的亚乙烯基时，则-X-CH 2 -Z不是-X 1 - 2 - -CH 2 - ，其中X 1表示硫或任选取代的氮，X 2表示任选取代的亚乙基）]} 或其盐的特征在于，在含有碳酸二酯的溶剂中使式（II）表示的化合物或其盐（其中符号具有与上述相同的含义）进行闭环反应。

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