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    • 1. 发明授权
    • Method for producing optically active 3-aminopiperidine or salt thereof
    • 光学活性3-氨基哌啶或其盐的制备方法
    • US08338142B2
    • 2012-12-25
    • US12449645
    • 2008-02-18
    • Kohei MoriMasutoshi NojiriAkira NishiyamaNaoaki Taoka
    • Kohei MoriMasutoshi NojiriAkira NishiyamaNaoaki Taoka
    • C12P17/12
    • C07D211/60C07B57/00C07D211/56C12P17/12C12P41/006
    • The present invention relates to a method for producing an optically active 3-aminopiperidine or salt thereof. In the method, a racemic nipecotamide is stereoselectively hydrolyzed to obtain an optically active nipecotamide and an optically active nipecotic acid in the presence of an enzyme source derived from an organism, and then the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by aroylation, Hofmann rearrangement, deprotection of the amino group and further deprotection; or the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by selective protection with BOC, Hofmann rearrangement and further deprotection. It is possible by the present invention to produce an optically active 3-aminopiperidine or salt thereof useful as a pharmaceutical intermediate from an inexpensive and easily available starting material by easy method applicable to industrial manufacturing.
    • 本发明涉及一种光学活性3-氨基哌啶或其盐的制备方法。 在该方法中,外消旋的丙内酰胺立体选择性地水解,得到光生活性的哌甲酰胺和光学活性的啮齿二甲酸,在衍生自生物体的酶源存在下,然后将光学活性的哌甲酰胺衍生成光学活性的氨基哌啶或其盐 通过酰化,Hofmann重排,氨基脱保护和进一步去保护; 或通过用BOC,霍夫曼重排和进一步去保护的选择性保护将光学活性的哌甲酰胺衍生成光学活性氨基哌啶或其盐。 通过本发明可以通过适用于工业制造的容易的方法从廉价且容易获得的原料中制备用作药物中间体的光学活性3-氨基哌啶或其盐。
    • 2. 发明申请
    • METHOD FOR PRODUCING OPTICALLY ACTIVE 3-AMINOPIPERIDINE OR SALT THEREOF
    • 用于生产光学活性的3-氨基哌啶或其盐的方法
    • US20100105917A1
    • 2010-04-29
    • US12449645
    • 2008-02-18
    • Kohei MoriMasutoshi NojiriAkira NishiyamaNaoaki Taoka
    • Kohei MoriMasutoshi NojiriAkira NishiyamaNaoaki Taoka
    • C07D211/98C12P17/12C07D211/60
    • C07D211/60C07B57/00C07D211/56C12P17/12C12P41/006
    • The present invention relates to a method for producing an optically active 3-aminopiperidine or salt thereof. In the method, a racemic nipecotamide is stereoselectively hydrolyzed to obtain an optically active nipecotamide and an optically active nipecotic acid in the presence of an enzyme source derived from an organism, and then the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by aroylation, Hofmann rearrangement, deprotection of the amino group and further deprotection; or the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by selective protection with BOC, Hofmann rearrangement and further deprotection. It is possible by the present invention to produce an optically active 3-aminopiperidine or salt thereof useful as a pharmaceutical intermediate from an inexpensive and easily available starting material by easy method applicable to industrial manufacturing.
    • 本发明涉及一种光学活性3-氨基哌啶或其盐的制备方法。 在该方法中,外消旋的丙内酰胺立体选择性地水解,得到光生活性的哌甲酰胺和光学活性的啮齿二甲酸,在衍生自生物体的酶源存在下,然后将光学活性的哌甲酰胺衍生成光学活性的氨基哌啶或其盐 通过酰化,Hofmann重排,氨基脱保护和进一步去保护; 或通过用BOC,霍夫曼重排和进一步去保护的选择性保护将光学活性的哌甲酰胺衍生成光学活性氨基哌啶或其盐。 通过本发明可以通过适用于工业制造的容易的方法从廉价且容易获得的原料中制备用作药物中间体的光学活性3-氨基哌啶或其盐。
    • 6. 发明授权
    • Tandem type master cylinder
    • 串联式主缸
    • US5187934A
    • 1993-02-23
    • US758882
    • 1991-09-11
    • Kohei Mori
    • Kohei Mori
    • B60T11/20B60T11/236F16J15/18
    • F16J15/183B60T11/20B60T11/236
    • A tandem type master cylinder is disclosed having a housing with a through-bore defining an intermediate portion and opposed end portions. The diameter of each end portion is larger than the diameter of the intermediate portion, and the junctures between the end portions and the intermediate portion define step parts within the housing. Seal assemblies are positioned within the housing at the step junctures formed by the intermediate portion and the end portions and are retained in position by a plug secured within each end portion. Primary and Secondary pistons are disposed for guided movement along the intermediate portion of the housing, and return springs are provided within the housing for urging each piston to its initial rest position.
    • 公开了一种串联式主缸,具有具有限定中间部分和相对端部的通孔的壳体。 每个端部的直径大于中间部分的直径,并且端部和中间部分之间的接合部限定了壳体内的台阶部分。 密封组件在由中间部分和端部形成的台阶接合处定位在壳体内,并且通过固定在每个端部内的插塞保持就位。 主活塞和次级活塞设置成沿着壳体的中间部分引导运动,并且复位弹簧设置在壳体内,用于将每个活塞推到其初始静止位置。
    • 8. 发明授权
    • Brake booster
    • 制动助力器
    • US4619185A
    • 1986-10-28
    • US684450
    • 1984-12-21
    • Kohei MoriHaruo Suzuki
    • Kohei MoriHaruo Suzuki
    • B60T13/563B60T13/57F15B9/10
    • B60T13/57
    • A brake booster includes a plunger which defines a valve mechanism. A stop member is provided to prevent the withdrawal of the plunger, and structure is provided to prevent the disengagement of the stop member from a valve body. Specifically, the valve body is formed with a detent, and a retainer which supports the stop member is formed with a detent which is engageable with the detent on the valve body. The retainer is disposed externally of the stop member, and the detents on both the valve body and the retainer are effective, when engaged, to prevent the disengagement of the stop member from the valve body.
    • 制动助力器包括限定阀机构的柱塞。 提供止动构件以防止柱塞的抽出,并且提供结构以防止止动构件从阀体脱离。 具体地,阀体形成有止动件,并且支撑止动构件的保持器形成有可与阀体上的止动件接合的制动器。 保持器设置在止动构件的外部,并且当接合时,阀体和保持器上的棘爪是有效的,以防止止动构件从阀体脱离。