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51. 发明申请

US20050190427A1 Method and apparatus for transmitting energy via a laser beam 有权
标题翻译：通过激光束传输能量的方法和装置
公开(公告)号：US20050190427A1
公开(公告)日：2005-09-01
申请号：US11040827
申请日：2005-01-20
申请人： Frank Steinsiek , Karl-Heinz Weber , Wolf-Peter Foth , Hans-Jochen Foth , Christian Schaefer
发明人： Frank Steinsiek , Karl-Heinz Weber , Wolf-Peter Foth , Hans-Jochen Foth , Christian Schaefer
IPC分类号： G02B26/08 , B64G1/42 , H02J17/00 , H04B10/118 , H04B10/80 , G01C3/08 , G02B5/12 , G02B26/00 , G02F1/00 , G02F1/01
CPC分类号： H04B10/806 , B64G1/428 , H02J7/025 , H02J17/00 , H02J50/30 , H02J50/90 , H04B10/118
摘要： To transmit energy without direct mechanical or electrical contact, a transmitter unit emits a laser beam onto a radiation receiver of a receiver unit including a photovoltaic cell arrangement surrounded by a ring-shaped reflector. A portion of the laser beam is reflected from the reflector back to the transmitter unit, where the received reflected signal is evaluated to determine the position of the laser beam impinging on the radiation receiver. The transmitter unit deflects the laser beam as necessary to impinge directly on the photovoltaic cell arrangement and track any relative motion of the receiver unit. The receiver unit orients the radiation receiver to optimize the energy reception. The position of the laser beam is modulated and the resulting variation of the reflected signal is evaluated to determine therefrom the position of the laser beam on the radiation receiver.
摘要翻译：为了在没有直接机械或电接触的情况下传输能量，发射器单元将激光束发射到包括由环形反射器包围的光伏电池装置的接收器单元的辐射接收器上。激光束的一部分从反射器反射回发射器单元，其中评估所接收的反射信号以确定激光束照射在辐射接收器上的位置。发射器单元根据需要使激光束偏转以直接照射在光伏电池装置上并跟踪接收器单元的任何相对运动。接收器单元定向辐射接收器以优化能量接收。对激光束的位置进行调制，并且评估所得到的反射信号的变化，从而确定激光束在辐射接收器上的位置。

52. 发明授权

US5753647A Acylamino-substituted hetrazepines 失效
标题翻译：酰氨基取代的hetrazepines
公开(公告)号：US5753647A
公开(公告)日：1998-05-19
申请号：US350196
申请日：1994-12-05
申请人： Karl-Heinz Weber , Werner Stransky , Ulrike Kufner-Muhl , Hubert Heuer , Franz Birke
发明人： Karl-Heinz Weber , Werner Stransky , Ulrike Kufner-Muhl , Hubert Heuer , Franz Birke
IPC分类号： A61K31/55 , A61P1/04 , A61P9/00 , A61P11/00 , A61P29/00 , A61P37/08 , C07C45/49 , C07D495/14 , C07D495/22
CPC分类号： C07D495/14 , C07C45/49 , C07D495/22
摘要： A hetrazepine of the formula given below and a pharmaceutical composition comprising a therapeutically effective amount of the hetrazepine and a pharmaceutically acceptable inert carrier are disclosed and are useful in treating disease in a warm-blooded animal induced by endogenously formed PAF; ##STR1## wherein the substituents are defined herein.
摘要翻译：公开了以下给出的公式的噻替平，以及包含治疗有效量的他唑嗪和药学上可接受的惰性载体的药物组合物，可用于治疗由内源性形成的PAF诱导的温血动物中的疾病; 其中取代基在本文中定义。

53. 发明授权

US5422353A Tetrahydropyridine derivatives 失效
标题翻译：四氢吡啶衍生物
公开(公告)号：US5422353A
公开(公告)日：1995-06-06
申请号：US145264
申请日：1993-10-29
申请人： Gerhard Walther , Karl-Heinz Weber , Werner Stransky , Franz J. Kuhn , Erich Lehr , Enzio Muller , Gunter Schingnitz , Helmut Ensinger
发明人： Gerhard Walther , Karl-Heinz Weber , Werner Stransky , Franz J. Kuhn , Erich Lehr , Enzio Muller , Gunter Schingnitz , Helmut Ensinger
IPC分类号： A61K31/00 , A61K31/44 , A61K31/445 , A61K31/4465 , A61P25/02 , A61P25/28 , A61P43/00 , C07D211/70 , A61K31/435 , C07D211/82
CPC分类号： C07D211/70
摘要： The invention relates to new tetrahydropyridine derivatives, processes for preparing them and their use as pharmaceutical compositions with cholinomimetic properties.
摘要翻译：本发明涉及新的四氢吡啶衍生物，其制备方法及其作为药物组合物具有胆碱性质的用途。

54. 发明授权

US5251012A Electro-optical scanner 失效
标题翻译：电光扫描仪
公开(公告)号：US5251012A
公开(公告)日：1993-10-05
申请号：US743529
申请日：1991-08-09
申请人： Johannes Riegger , Karl-Heinz Weber
发明人： Johannes Riegger , Karl-Heinz Weber
IPC分类号： G01D5/347 , G06K7/10 , H03M1/24 , G01B11/14
CPC分类号： H03M1/245 , G01D5/34723 , G01D5/34792 , G06K7/10702
摘要： An electro-optical scanner, particularly for position-, angle- and rotation-measuring instruments as well as for optical storages, comprising an illuminated or transilluminated code carrier (5), at least one optically scannable code track on the code carrier, an optical system (7) recording the code track, and an electro-optical sensor (8), with the optical system reproducing the code track on a light-sensitive surface of the sensor, should be easily manufactured, installed and adjusted, should comprise reduced dimensions, especially a smaller working distance and should allow a better position information. Thereto, the optical system comprises at least one rod-shaped lens (13) or a micro-lens plate.
摘要翻译：一种电光扫描仪，特别是用于位置，角度和旋转测量仪器以及用于光学存储器的电光扫描器，其包括照明或透照的码载体（5），代码载体上的至少一个可光学扫描的码轨道，光学记录代码轨道的系统（7）以及在传感器的感光表面上再现代码轨道的光学系统的电光传感器（8）应当容易地制造，安装和调整，包括减小的尺寸特别是较小的工作距离，应该允许更好的位置信息。此外，光学系统包括至少一个棒状透镜（13）或微透镜板。

55. 发明授权

US4996224A 1-benzyl-4- or 5-pyrrolidinomethyl-pyrrolidin-2-ones and nootropic method of use thereof 失效
标题翻译： 1-苄基-4-或5-吡咯烷基甲基 - 吡咯烷-2-酮及其有用的方法
公开(公告)号：US4996224A
公开(公告)日：1991-02-26
申请号：US350597
申请日：1989-05-11
申请人： Karl-Heinz Weber , Gerhard Walther , Claus Schneider , Dieter Hinzen , Franz J. Kuhn , Erich Lehr
发明人： Karl-Heinz Weber , Gerhard Walther , Claus Schneider , Dieter Hinzen , Franz J. Kuhn , Erich Lehr
IPC分类号： A61K31/40 , A61K31/4015 , A61K31/415 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/495 , A61K31/535 , A61P25/02 , A61P25/04 , A61P25/28 , C07D207/12 , C07D207/26 , C07D207/27 , C07D401/06 , C07D403/06 , C07D521/00
CPC分类号： C07D207/26 , C07D231/12 , C07D233/56 , C07D249/08 , C07D401/06
摘要： Compounds of the formula ##STR1## wherein R.sub.1 is hydrogen or alkyl of 1 to 4 carbon atoms;R.sub.2 is 2-, 3- or 4-pyridyl, phenyl or mono- or di- substituted phenyl, where the substituents are each individually alkoxy of 1 to 2 carbon atoms, fluorine, chlorine, bromine, trifluoromethyl, alkyl or 1 to 4 carbon atoms, hydroxyl or nitro; andR.sub.3 and R.sub.4 are each independently hydrogen or alkyl of 1 to 4 carbon atoms; orR.sub.3 and R.sub.4, together with each other and the nitrogen atom to which they are attached, form an unsubstituted or methyl-substituted, saturated 5- or 6-membered heterocycle which may contain an additional oxygen or nitrogen heteroatom, or form an imidazole ring;where the aminomethyl substituent is attached to the 4- or 5-position or the pyrrolidine ring, and non-toxic, pharmacologically acceptable acid addition salts thereof. The compounds as well as the salts are useful as nootropics and antihypoxics.

56. 发明授权

US4954516A Use of 1-benzyl-aminoalkyl-pyrrolidinones as antidepressants 失效
公开(公告)号：US4954516A
公开(公告)日：1990-09-04
申请号：US383105
申请日：1989-07-20
申请人： Erich Lehr , Wolf-Dietrich Bechtel , Karin Boke-Kuhn , Claus Schneider , Gerhard Walther , Karl-Heinz Weber
发明人： Erich Lehr , Wolf-Dietrich Bechtel , Karin Boke-Kuhn , Claus Schneider , Gerhard Walther , Karl-Heinz Weber
IPC分类号： A61K31/40 , A61K31/4015 , A61K31/415 , A61K31/42 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/495 , A61K31/535 , A61P25/24 , A61P25/26 , C07D207/09 , C07D207/267 , C07D207/27 , C07D401/06 , C07D403/06
CPC分类号： A61K31/40 , A61K31/415 , A61K31/42 , A61K31/44 , A61K31/445 , A61K31/495 , A61K31/535
摘要： The invention relates to the use of 1-benzyl-aminoalkyl-pyrrolidinones as antidepressants.

57. 发明授权

US4891378A Nortropanyl containing pyrrolidinones, pharmaceutical compositions and use 失效
标题翻译：含鸟嘌呤的吡咯烷酮，药物组合物和用途
公开(公告)号：US4891378A
公开(公告)日：1990-01-02
申请号：US365169
申请日：1989-06-12
申请人： Karl-Heinz Weber , Claus Schneider , Gerhard Walther , Dieter Hinzen , Franz J. Kuhn , Erich Lehr , Helmut Ensinger , Wolfgang Troger
发明人： Karl-Heinz Weber , Claus Schneider , Gerhard Walther , Dieter Hinzen , Franz J. Kuhn , Erich Lehr , Helmut Ensinger , Wolfgang Troger
IPC分类号： A61K31/40 , A61K31/4015 , A61K31/4427 , A61K31/445 , A61K31/495 , A61K31/535 , A61P25/00 , A61P25/28 , C07D207/26 , C07D401/12 , C07D413/12 , C07D451/02 , C07D487/08
CPC分类号： C07D207/26 , C07D401/12 , C07D413/12 , C07D451/02
摘要： The invention relates to new substituted pyrrolidinones of general formula ##STR1## wherein R.sub.1 represents a phenyl group which may be mono- or di-substituted by methyl, methoxy, fluorine, chlorine, bromine or trifluoromethyl, or a pyridyl group;R.sub.2 represents hydrogen or a straight-chained or branched alkyl group with 1-4 carbon atoms;R.sub.3 represents a straight-chained or branched alkyl group with 1-3 carbon atoms, a hydroxyalkyl group with 2-3 carbon atoms, a phenyl group which can be mono- or di-substituted by chlorine, bromine, methyl or methoxy, a cyclohexyl group or a dialkylamino alkyl group, where in each alkyl group can contain from 1-3 carbon atoms;R.sub.4 represents hydrogen or a straight-chained or branched alkyl group with 1-3 carbon atoms; orR.sub.3 and R.sub.4 together with the nitrogen atom represent a piperidine, morpholine or piperazine ring, while the ring may be substituted by 1 or 2 methyl groups and the piperazine ring at the nitrogen atom in 4-position may also carry a phenyl, chlorophenyl or benzyl group, or they may represent the nortropanyl group, processes for preparing them and pharmaceutical compositions.The new compounds have proved effective in animal trials in alleviating or remedying conditions or restricted cerebral performance.

58. 发明授权

US4857528A Substituted pyrrolidinones, pharmaceutical compositions and use 失效
标题翻译：取代的吡咯烷酮，药物组合物和用途
公开(公告)号：US4857528A
公开(公告)日：1989-08-15
申请号：US183819
申请日：1988-04-20
申请人： Karl-Heinz Weber , Claus Schneider , Gerhard Walther , Dieter Hinzen , Franz J. Kuhn , Erich Lehr , Helmut Ensinger , Wolfgang Troger
发明人： Karl-Heinz Weber , Claus Schneider , Gerhard Walther , Dieter Hinzen , Franz J. Kuhn , Erich Lehr , Helmut Ensinger , Wolfgang Troger
IPC分类号： A61K31/40 , A61K31/4015 , A61K31/4427 , A61K31/445 , A61K31/495 , A61K31/535 , A61P25/00 , A61P25/28 , C07D207/26 , C07D401/12 , C07D413/12 , C07D451/02 , C07D487/08
CPC分类号： C07D207/26 , C07D401/12 , C07D413/12 , C07D451/02
摘要： The invention relates to substituted pyrrolidinones of general formula ##STR1## wherein R.sub.1 represents a phenyl group which may be mono- or di-substituted by methyl, methoxy, fluorine, chlorine, bromine or trifluoromethyl, or a pyridyl group;R.sub.2 represents hydrogen or a straight-chained or branched alkyl group with 1-4 carbon atoms;R.sub.3 represents a straight-chained or branched alkyl group with 1-3 carbon atoms, a hydroxyalkyl group with 2-3 carbon atoms, a phenyl group which can be mono- or di-substituted by chlorine, bromine, methyl or methoxy, a cyclohexyl group or a dialkylamino alkyl group, where in each alkyl group can contain from 1-3 carbon atoms;R.sub.4 represents hydrogen or a straight-chained or branched alkyl group with 1-3 carbon atoms; orR.sub.3 and R.sub.4 together with the nitrogen atom represent a piperidine, morpholine or piperazine ring, while the ring may be substituted by 1 or 2 methyl groups and the piperazine ring at the nitrogen atom in 4-position may also carry a phenyl, chlorophenyl or benzyl group, or they may represent the nortropanyl group, processes for preparing them and pharmaceutical compositions.The new compounds have proved effective in animal trials in alleviating or remedying conditions or restricted cerebral performance.
摘要翻译：本发明涉及通式为（1）的取代吡咯烷酮，其中R 1表示可被甲基，甲氧基，氟，氯，溴或三氟甲基或吡啶基单取代或二取代的苯基; R 2表示氢或具有1-4个碳原子的直链或支链烷基; R3表示具有1-3个碳原子的直链或支链烷基，具有2-3个碳原子的羟烷基，可被氯，溴，甲基或甲氧基单取代或二取代的苯基，环己基基团或二烷基氨基烷基，其中在每个烷基中可以含有1-3个碳原子; R4表示氢或具有1-3个碳原子的直链或支链烷基; 或者R3和R4与氮原子一起代表哌啶，吗啉或哌嗪环，而环可以被1或2个甲基取代，4-位氮原子上的哌嗪环也可以带有苯基，氯苯基或或它们可以代表异丙基丙基，其制备方法和药物组合物。新化合物已被证明在动物试验中有效减轻或补救病症或限制脑部表现。

59. 发明授权

US4833140A 1-(benzyl or pyridylmethyl)-4 or 5-aminomethyl-pyrrolidin-2-ones 失效
标题翻译： 1-（苄基或吡啶基甲基）-4或5-氨基甲基 - 吡咯烷-2-酮
公开(公告)号：US4833140A
公开(公告)日：1989-05-23
申请号：US199291
申请日：1988-05-26
申请人： Karl-Heinz Weber , Gerhard Walther , Claus Schneider , Dieter Hinzen , Franz J. Kuhn , Erich Lehr
发明人： Karl-Heinz Weber , Gerhard Walther , Claus Schneider , Dieter Hinzen , Franz J. Kuhn , Erich Lehr
IPC分类号： A61K31/40 , A61K31/4015 , A61K31/415 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/495 , A61K31/535 , A61P25/02 , A61P25/04 , A61P25/28 , C07D207/12 , C07D207/26 , C07D207/27 , C07D401/06 , C07D403/06 , C07D521/00
CPC分类号： C07D207/26 , C07D231/12 , C07D233/56 , C07D249/08 , C07D401/06
摘要： Compounds of the formula ##STR1## wherein R.sub.1 is hydrogen or alkyl of 1 to 4 carbon atoms;R.sub.2 is 2-, 3- or 4-pyridyl, phenyl or mono- or disubstituted phenyl, where the substituents are each individually alkoxy of 1 to 2 carbon atoms, fluorine, chlorine, bromine, trifluoromethyl, alkyl or 1 to 4 carbon atoms, hydroxyl or nitro; andR.sub.3 and R.sub.4 are each independently hydrogen or alkyl of 1 to 4 carbon atoms; orR.sub.3 and R.sub.4, together with each other and the nitrogen atom to which they are attached, form an unsubstituted or methyl-substituted, saturated 5- or 6-membered heterocycle which may contain an additional oxygen or nitrogen heteroatom, or form an imidazole ring;where the aminomethyl substituent is attached to the 4- or 5-position or the pyrrolidine ring, and non-toxic, pharmacologically acceptable acid addition salts thereof. The compounds as well as the salts are useful as nootropics and antihypoxics.
摘要翻译：其中R 1为氢或1至4个碳原子的烷基的式IMA化合物; R 2是2-，3-或4-吡啶基，苯基或单取代或二取代的苯基，其中取代基各自为1至2个碳原子的烷氧基，氟，氯，溴，三氟甲基，烷基或1至4个碳原子，羟基或硝基; 并且R 3和R 4各自独立地为氢或1至4个碳原子的烷基; 或R 3和R 4彼此连接并与它们所连接的氮原子形成未取代的或甲基取代的饱和的5-或6-元杂环，其可以含有另外的氧或氮杂原子，或形成咪唑环 ; 其中氨基甲基取代基连接到4-或5-位或吡咯烷环上，以及无毒的药学上可接受的酸加成盐。这些化合物以及盐类可用作神经递质和抗缺氧剂。

60. 发明授权

US4767759A Piperazinyl and morpholinyl substituted 1-(benzyl or pyridylmethyl)-4-or-5-aminomethyl-pyrrolidin-2-ones and their nootropic use 失效
标题翻译：哌嗪基和吗啉基取代的1-（苄基或吡啶基甲基）-4-或5-氨基甲基 - 吡咯烷-2-酮及其适应症用途
公开(公告)号：US4767759A
公开(公告)日：1988-08-30
申请号：US878828
申请日：1986-06-26
申请人： Karl-Heinz Weber , Gerhard Walther , Claus Schneider , Dieter Hinzen , Franz J. Kuhn , Erich Lehr
发明人： Karl-Heinz Weber , Gerhard Walther , Claus Schneider , Dieter Hinzen , Franz J. Kuhn , Erich Lehr
IPC分类号： A61K31/40 , A61K31/4015 , A61K31/415 , A61K31/44 , A61K31/4427 , A61K31/445 , A61K31/495 , A61K31/535 , A61P25/02 , A61P25/04 , A61P25/28 , C07D207/12 , C07D207/26 , C07D207/27 , C07D401/06 , C07D403/06 , C07D521/00 , C07D413/06
CPC分类号： C07D207/26 , C07D231/12 , C07D233/56 , C07D249/08 , C07D401/06
摘要： Compounds of the formula ##STR1## wherein R.sub.1 is hydrogen or alkyl of 1 to 4 carbon atoms;R.sub.2 is 2-, 3- or 4-pyridyl, phenyl or mono- or di- substituted phenyl, where the substituents are each individually alkoxy of 1 to 2 carbon atoms, fluorine, chlorine, bromine, trifluoromethyl, alkyl or 1 to 4 carbon atoms, hydroxyl or nitro; andR.sub.3 and R.sub.4 are each independently hydrogen or alkyl of 1 to 4 carbon atoms; orR.sub.3 and R.sub.4, together with each other and the nitrogen atom to which they are attached, form an unsubstituted or methyl-substituted, saturated 5- or 6-membered heterocycle which may contain an additional oxygen or nitrogen heteroatom, or form an imidazole ring;where the aminomethyl substituent is attached to the 4- or 5-position or the pyrrolidine ring, and non-toxic, pharmacologically acceptable acid addition salts thereof. The compounds as well as the salts are useful as nootropics and antihypoxics.
摘要翻译：其中R 1为氢或1至4个碳原子的烷基的式IMA化合物; R2是2-，3-或4-吡啶基，苯基或单取代或二取代的苯基，其中取代基各自为1至2个碳原子的烷氧基，氟，氯，溴，三氟甲基，烷基或1至4碳原子，羟基或硝基; 并且R 3和R 4各自独立地为氢或1至4个碳原子的烷基; 或R 3和R 4彼此连接并与它们所连接的氮原子形成未取代的或甲基取代的饱和的5-或6-元杂环，其可以含有另外的氧或氮杂原子，或形成咪唑环 ; 其中氨基甲基取代基连接到4-或5-位或吡咯烷环上，以及无毒的药学上可接受的酸加成盐。这些化合物以及盐类可用作神经递质和抗缺氧剂。

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