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1. 发明授权

US4805348A Flat lapping machine 失效
标题翻译：平面研磨机
公开(公告)号：US4805348A
公开(公告)日：1989-02-21
申请号：US891241
申请日：1986-07-29
申请人： Hatsuyuki Arai , Isao Nagahashi , Seiichi Maeda , Kazumi Yasuda , Shiro Furusawa , Kazuhiko Hirata , Kastunori Nagao , Kazuhiko Kondo , Takaya Sanoki , Misuo Sugiyama , Shinichi Kusano
发明人： Hatsuyuki Arai , Isao Nagahashi , Seiichi Maeda , Kazumi Yasuda , Shiro Furusawa , Kazuhiko Hirata , Kastunori Nagao , Kazuhiko Kondo , Takaya Sanoki , Misuo Sugiyama , Shinichi Kusano
IPC分类号： B24B37/08 , B24B37/28 , B24B7/00
CPC分类号： B24B37/28 , B24B37/08
摘要： Described herein is a flat lapping machine capable of precision-abrading simultaneously flat surfaces on the front and rear sides of a work in the fashion of lapping, polishing and grinding machines. The present invention contemplates to provide a flat lapping machine which is simplified in construction as compared with conventional flap lapping machines having a large number of carriers in planetary motions, and which can stop the respective carriers easily in specific positions and directions at the end of a lapping operation. To this end, the present invention employs a large number of support gear mechanisms each constituted by a plural number of small gears and located at uniform intervals around a center gear, rotatably supporting the respective carriers in predetermined positions while the respective carriers are driven by the center gear.
摘要翻译：这里描述的是能够以研磨，抛光和研磨机器的方式同时精确研磨工件的前后两侧的平坦表面的平板研磨机。本发明旨在提供一种与具有行星运动中的大量载体的常规翼片研磨机相比，其结构简化的平板研磨机，其能够在特定位置和方向上容易地停止相应的载体研磨操作。为此，本发明采用大量支撑齿轮机构，每个支撑齿轮机构由多个小齿轮构成，并且围绕中心齿轮以均匀的间隔设置，可旋转地支撑各个载体在预定位置，同时各个载体由中心齿轮

2. 发明授权

US5589592A Process for preparing .beta.-lactam derivative and synthetic intermediate 失效
标题翻译：制备β-内酰胺衍生物和合成中间体的方法
公开(公告)号：US5589592A
公开(公告)日：1996-12-31
申请号：US393395
申请日：1995-04-07
申请人： Hiroshi Horikawa , Kazuhiko Kondo
发明人： Hiroshi Horikawa , Kazuhiko Kondo
IPC分类号： C07D463/00 , C07D477/00 , C07D477/02 , C07D477/04 , C07D499/06 , C07D499/88 , C07D499/893 , C07D499/897 , C07D501/16 , C07D501/18 , C07D503/04 , C07D505/00 , C07D513/04 , C07D515/04
CPC分类号： C07D513/04 , C07D477/02 , C07D477/04 , C07D515/04
摘要： Disclosed is a process for preparing a .beta.-lactam compound represented by the formula: ##STR1## wherein R.sup.1 represents a hydroxy-substituted lower alkyl group or an amino group each of which may be protected; R.sup.2 represents hydrogen atom or an ester residue; X represents a methylene group which may be substituted by a lower alkyl group, sulfur atom or a group represented by the formula: --A--CH.sub.2 -- where A represents sulfur atom, oxygen atom or methylene group; and W represents an active ester residue of hydroxyl group,or a salt thereof, which comprises the steps of treating a 1-aza-3-thia-bicycloalkane compound represented by the formula: ##STR2## wherein R.sup.1, R.sup.2 and X have the same meanings as defined above, or a salt thereof with a base in the presence of a desulfurizing agent and then reacting the resulting compound with an active esterifying agent of hydroxyl group.
摘要翻译：公开了一种制备由下式表示的β-内酰胺化合物的方法：其中R 1表示羟基取代的低级烷基或各自可被保护的氨基; R2表示氢原子或酯残基; X表示可以被低级烷基，硫原子或由下式表示的基团取代的亚甲基：-A-CH2-，其中A表示硫原子，氧原子或亚甲基; W表示羟基的活性酯残基或其盐，其包括如下步骤：处理由下式表示的1-氮杂-3-硫杂 - 双环烷烃化合物：其中R1，R2和X 具有与上述相同的含义，或其盐与脱碱剂存在下的碱，然后使所得化合物与羟基的活性酯化剂反应。

3. 发明授权

US07932456B2 Music replay circuit 有权
标题翻译：音乐回放电路
公开(公告)号：US07932456B2
公开(公告)日：2011-04-26
申请号：US12240602
申请日：2008-09-29
申请人： Kazuhiko Kondo
发明人： Kazuhiko Kondo
IPC分类号： G10H7/00
CPC分类号： G11B20/10009 , G10L21/038 , G11B20/10046 , G11B20/10481 , G11B20/10527 , G11B2020/00028 , G11B2020/00057
摘要： A music replay circuit is provided which includes a header analyzing unit which analyzes a header included in each of a plurality of frames in a data stream which are compressed music data and extracts bitrate information included in the header, a decoder which decodes the data stream analyzed by the header analyzing unit, a high-frequency correction unit which generates data in which high-frequency music data is interpolated, for music data decoded by the decoder, and a process setting unit which controls the process applied by the high-frequency correction unit based on the bitrate information extracted by the header analyzing unit, wherein the process setting unit control the process by the high-frequency correction unit according to the bitrate information extracted for each frame.
摘要翻译：提供了一种音乐重播电路，其包括头部分析单元，该头部分析单元分析包括在压缩音乐数据的数据流中的多个帧中的每一帧中的头部，并提取包括在头部中的比特率信息;解码器，对分析的数据流进行解码通过标题分析单元，生成用于对由解码器解码的音乐数据进行内插的高频音乐数据的数据的高频校正单元，以及控制由高频校正单元施加的处理的处理设置单元基于由标题分析单元提取的比特率信息，其中处理设置单元根据针对每个帧提取的比特率信息来控制高频校正单元的处理。

4. 发明授权

US5587474A Method for removing the protecting group for carboxyl group 失效
标题翻译：去除羧基保护基的方法
公开(公告)号：US5587474A
公开(公告)日：1996-12-24
申请号：US77383
申请日：1993-06-17
申请人： Kazuhiko Kondo , Hiroshi Horikawa , Tameo Iwasaki
发明人： Kazuhiko Kondo , Hiroshi Horikawa , Tameo Iwasaki
IPC分类号： C07D463/00 , C07D477/08 , C07D499/88 , C07D501/00 , C07D503/00 , C07D505/00 , C07D403/12
CPC分类号： C07D501/00 , C07D463/06 , C07D477/08 , C07D499/88 , C07D503/00 , C07D505/00 , Y02P20/55
摘要： A method for removing substituted or unsubstituted allyl group from .beta.-lactam compound having substituted or unsubstituted allyl group-protecting carboxyl group, which comprises treating said .beta.-lactam compound with palladium catalyst in the presence of allyl-scavenger in aqueous organic solvent, by which the substituted or unsubstituted group can be easily and effectively removed under moderate conditions so that the desired compound can be obtained in high yield at low cost.
摘要翻译：一种从具有取代或未取代的烯丙基保护羧基的β-内酰胺化合物中除去取代或未取代的烯丙基的方法，该方法包括在含有机溶剂的烯丙基清除剂存在下用钯催化剂处理所述β-内酰胺化合物，取代或未取代的基团可以在中等条件下容易且有效地除去，从而可以低成本高收率地获得所需化合物。

5. 发明授权

US5495012A Process for preparing optically active 4-mercapto-2-pyrrolidone derivative and intermediate therefor 失效
标题翻译：光学活性4-巯基-2-吡咯烷酮衍生物及其中间体的制备方法
公开(公告)号：US5495012A
公开(公告)日：1996-02-27
申请号：US409410
申请日：1995-03-24
申请人： Tameo Iwasaki , Kazuhiko Kondo , Tadashi Nakatani , Ryuzo Yoshioka
发明人： Tameo Iwasaki , Kazuhiko Kondo , Tadashi Nakatani , Ryuzo Yoshioka
IPC分类号： C07B57/00 , C07C309/24 , C07C319/28 , C07C323/58 , C07D207/26 , C07D207/273 , C07D477/02 , C07C309/14 , C07C323/25
CPC分类号： C07D207/273 , C07B57/00 , C07C309/24 , C07C319/28 , C07C323/58 , C07D477/02 , Y02P20/55
摘要： A process for preparing an optically active 4-mercapto-2-pyrrolidone derivative of the formula [I]: ##STR1## wherein R.sup.1 is a hydrogen atom or a protecting group and R.sup.2 is a hydrogen atom or a protecting group, which comprises subjecting racemic 4-amino-3-mercaptobutyric acid or a salt thereof to optical resolution by using 1-(trichlorophenyl)ethanesulfonic acid, followed by subjecting the product to cyclization reaction after protecting the functional groups thereof, if necessary, and further optionally removing the protecting groups therefrom. The present process is industrially advantageous than conventional processes for preparing optically active 4-mercapto-2-pyrrolidone derivatives which are useful as an intermediate for various medicines such as carbapenem antibacterial agents.
摘要翻译：制备式[I]的光学活性4-巯基-2-吡咯烷酮衍生物的方法：保护基，R 2是氢原子或保护基，其包括使外消旋的4-氨基-3-巯基丁酸或其盐通过使用1-（三氯苯基）乙磺酸进行光学拆分，随后如果需要，保护其官能团之后使产物进行环化反应，并进一步任选地从其中除去保护基。本方法在工业上比用于制备光学活性的4-巯基-2-吡咯烷酮衍生物的方法是有用的，其可用作各种药物例如碳青霉烯类抗菌剂的中间体。

6. 发明授权

US5442055A Azetidinone compound and process for preparation thereof 失效
标题翻译：氮杂环丁酮化合物及其制备方法
公开(公告)号：US5442055A
公开(公告)日：1995-08-15
申请号：US148917
申请日：1993-11-05
申请人： Tameo Iwasaki , Kazuhiko Kondo
发明人： Tameo Iwasaki , Kazuhiko Kondo
IPC分类号： C07D239/86 , A61K31/397 , A61K31/40 , A61K31/535 , A61K31/536 , A61K31/537 , A61P31/04 , C07D20060101 , C07D205/08 , C07D217/24 , C07D239/88 , C07D265/04 , C07D265/12 , C07D265/20 , C07D265/22 , C07D279/08 , C07D401/06 , C07D403/06 , C07D413/06 , C07D417/06 , C07D477/00 , C07D477/04 , C07D227/00
CPC分类号： C07D401/06 , C07D205/08 , C07D217/24 , C07D239/88 , C07D265/12 , C07D265/22 , C07D279/08 , C07D403/06 , C07D413/06 , C07D417/06 , C07D477/04
摘要： There is disclosed an azetidinone compound of the formula [I]: ##STR1## wherein Ring B is a benzene ring which may have substituent(s), R.sup.1 is a hydroxy-substituted lower alkyl group which may have substituent(s), X is oxygen atom and the like, Y is oxygen atom and the like, and Z is a methylene group which may have substituent(s), which is useful as a synthetic intermediate of the 1.beta.-methylcarbapenem-type antibacterial agent.
摘要翻译：公开了式[I]的氮杂环丁酮化合物：其中环B是可具有取代基的苯环，R 1是可具有取代基的羟基取代的低级烷基， X为氧原子等，Y为氧原子等，Z为可具有取代基的亚甲基，可用作1β-甲基碳青霉烯型抗菌剂的合成中间体。

7. 发明授权

US5412089A 2'-deoxy-2'-methylidenecytidine dihydrate, methods for its production and compositions 失效
标题翻译： 2'-脱氧-2'-亚甲基联嘧啶二水合物，其生产方法和组合物
公开(公告)号：US5412089A
公开(公告)日：1995-05-02
申请号：US959267
申请日：1992-10-09
申请人： Shinji Sakata , Takanori Miyashita , Kazuhiko Kondo
发明人： Shinji Sakata , Takanori Miyashita , Kazuhiko Kondo
IPC分类号： A61K9/00 , A61K31/70 , A61K31/7042 , A61K31/7052 , A61K31/7064 , A61K31/7068 , A61K47/12 , A61K47/26 , A61P31/12 , A61P35/00 , C07H19/06
CPC分类号： C07H19/06 , A61K47/12 , A61K47/26 , A61K9/0019
摘要： Novel stable, non-hygroscopic 2'-deoxy-2'-methylidenecytidine dihydrate and its methods for production, and compositions with improved solubility containing same and saccharide(s).
摘要翻译：新型稳定的，非吸湿性的2'-脱氧-2'-亚甲基联嘧啶二水合物及其制备方法，以及含有相同糖和糖的溶解度改善的组合物。

8. 发明授权

US5036471A Apparatus for road path searching applicable to car navigation system and operation method thereof 失效
标题翻译：适用于汽车导航系统的道路搜索装置及其运行方法
公开(公告)号：US5036471A
公开(公告)日：1991-07-30
申请号：US509991
申请日：1990-04-16
申请人： Yutaka Tamura , Yoshio Hosokawa , Satoshi Noro , Kazuhiko Kondo
发明人： Yutaka Tamura , Yoshio Hosokawa , Satoshi Noro , Kazuhiko Kondo
IPC分类号： G01C21/34 , G06F17/50
CPC分类号： G01C21/3446 , G01C21/32 , G06F17/509 , G06F17/5095
摘要： A road path searching apparatus applicable to a car navigation system is disclosed. Road map data with different level of detail for defining a predetermined area is stored previously in a memory device. First, nodes Nai and Nbj adjacent to each of the search nodes Pa and PB are detected based on map data having a high level of detail. When nodes Nai and Nbj exist on a map of a lower level of detail, a map of one lower level of detail is selected as a map to be used in the searching process. Accordingly, as following searching process is performed based on the map data of lower level of detail, required processing time is reduced.

9. 发明授权

US08073089B2 Data player and data play method 有权
标题翻译：数据播放器和数据播放方式
公开(公告)号：US08073089B2
公开(公告)日：2011-12-06
申请号：US12047375
申请日：2008-03-13
申请人： Kazuhiko Kondo
发明人： Kazuhiko Kondo
IPC分类号： H04L7/02
CPC分类号： H04L7/042
摘要： A synchronous pattern detection section checks coincidence between a predetermined reference synchronous pattern and a bit pattern included in a data stream. Each time a bit pattern which coincides with the reference synchronous pattern is detected, the synchronous pattern detection section extracts a frame length of a data frame corresponding to the bit pattern which is detected, and stores the extracted frame length in a storage section. Each time a bit pattern which coincides with the reference synchronous pattern is detected in the synchronous pattern detection section, a synchronization determination section determines whether or not the bit pattern detected by the synchronous pattern detection section is a correct synchronous pattern, based on a plurality of frame lengths stored in the storage section and a bit length of a data stream which is obtained after detection of the bit pattern. With this structure, a synchronous pattern included in the data stream can be detected with higher precision.
摘要翻译：同步模式检测部分检查预定参考同步模式和包括在数据流中的位模式之间的一致性。每次检测到与参考同步模式一致的位模式时，同步模式检测部分提取与检测到的位模式相对应的数据帧的帧长度，并将所提取的帧长度存储在存储部分中。每当同步模式检测部分检测到与参考同步模式一致的位模式时，同步确定部分基于多个模式检测部分确定由同步模式检测部件检测到的位模式是否是正确的同步模式存储在存储部分中的帧长度和在检测到位模式之后获得的数据流的位长度。利用这种结构，可以更高精度地检测包括在数据流中的同步模式。

10. 发明授权

US07439368B2 Process for producing 3-acylaminobenzofuran-2-carboxylic acid derivative 失效
标题翻译： 3-酰氨基苯并呋喃-2-羧酸衍生物的制备方法
公开(公告)号：US07439368B2
公开(公告)日：2008-10-21
申请号：US10561180
申请日：2004-06-29
申请人： Masahiko Seki , Shin-ichi Yoshida , Nobuhiro Yagi , Masanori Hatsuda , Mayumi Kimura , Kazuhiko Kondo
发明人： Masahiko Seki , Shin-ichi Yoshida , Nobuhiro Yagi , Masanori Hatsuda , Mayumi Kimura , Kazuhiko Kondo
IPC分类号： C07D405/14 , C07D405/12
CPC分类号： C07D405/14 , C07C253/14 , C07D207/27 , C07D211/76 , C07D213/57 , C07D213/85 , C07D265/32 , C07D295/192 , C07D333/62 , C07D333/68 , C07D405/12 , C07C255/50 , C07C255/51 , C07C255/53 , C07C255/54 , C07C255/56 , C07C255/57
摘要： The present invention provides a process of preparing a compound of the formula [I]: wherein X is a group of the formula: —N═ or —CH═; R1 is a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a cyano group or an amino group optionally substituted by a lower alkyl group; Ring A is a nitrogen-containing heterocyclic group; Ring B is an optionally substituted benzene ring or an optionally substituted pyridine ring; and R3 is a hydrogen atom or a lower alkyl group, or a pharmaceutically acceptable salt thereof, which is useful as an inhibitor of activated blood coagulation factor X.
摘要翻译：本发明提供制备式[I]化合物的方法：其中X是下式的基团：-N-或-CH-; R 1是氢原子，卤素原子，低级烷基，低级烷氧基，氰基或任选被低级烷基取代的氨基; 环A是含氮杂环基; 环B是任选取代的苯环或任选取代的吡啶环; R 3是氢原子或低级烷基或其药学上可接受的盐，其可用作活化凝血因子X的抑制剂。

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