CAS: 3690-04-8; N-(1,5-Dimethyl-3-Oxo-2-Phenyl-2,3-Dihydro-1H-Pyrazol-4-yl)-2-(Dimethylamino)Propanamide

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    CAS号83-07-8 4-氨基安替比林 | CAS号130515-23-0 Alanine, N,N-di... | CAS号82614-49-1 ethyl 2-(N,N-di... | CAS号124-40-3 二甲胺 | CAS号101937-73-9 2-Chloro-N-(1,5... | CAS号598-72-1 2-溴丙酸

    合成工艺路线路线简述

      📜4-氨基安替比林置于phosphorus Pentoxide,苯体系中,化学反应生成 氨丙吡酮
      参考文献:Takahashi Et Al.,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1955,Vol. 75,P. 1431,1432
      标题:Takahashi Et Al.,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1955,Vol. 75,P. 1431,1432

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      专利信息


      专利号:US-2024287041-A1
      优先权日:2021-05-20
      标题 :Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms
      发明人:BALOGLU ERKAN; AUSTAD BRIAN C; ROE DAVID G; KEDUC ANDREW; GOTTSCHLING STEPHEN EDMUND; HECKER EVAN
      权利人:KARYOPHARM THERAPEUTICS INC
      摘要:The present invention relates to a method of preparing a compound represented by structural formula (VII), comprising reacting a compound represented by structural formula (II), with a compound represented by structural formula (III), in a solvent, in the presence of a Pd catalyst and one or more inorganic bases under conditions suitable to prepare a compound represented by structural formula (VII): The values and example values of the variables in structural formulas (VII), (II), and (III) are defined herein. The present invention also relates to crystalline Forms I and II of the compound represented by Structural Formula (VII), the use of the crystalline Forms in treating disease or disorders associated with CRM1 and method of preparing the crystalline Forms.

      专利号:AU-2022276509-A1
      优先权日:2021-05-20
      标题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

      专利号:US-9994558-B2
      优先权日:2013-09-20
      标题 :Multicyclic compounds and methods of using same
      发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM; MCCAULEY DILARA; LANDESMAN YOSEF; GOLAN GALI; KALID ORI; SHECHTER SHARON
      权利人:KARYOPHARM THERAPEUTICS INC
      摘要:The invention generally relates to compounds represented by Structural Formula I: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula I, or a pharmaceutically acceptable salt or composition thereof, e.g., in treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders (e.g., PAK-mediated, for example, PAK4-mediated, diseases and disorders).

      专利号:US-7749985-B2
      优先权日:2006-09-15
      标 题 :Acyloxyalkyl carbamate prodrugs, methods of synthesis and use
      发明人:GALLOP MARK A; XU FENG; PHAN THU; DILIP USHA; PENG GE
      权利人:XENOPORT INC
      摘要:Acyloxyalkyl carbamate prodrugs of 3-aminopropylphosphinic acid and analogs thereof, methods of making acyloxyalkyl carbamate prodrugs of 3-aminopropylphosphinic acid and analogs thereof, methods of using acyloxyalkyl carbamate prodrugs of 3-aminopropylphosphinic acid and analogs thereof, and pharmaceutical compositions comprising acyloxyalkyl carbamate prodrugs 3-aminopropylphosphinic acid and analogs thereof for treating diseases or disorders such as mild cognitive impairment, cognitive impairment associated with Alzheimer's disease Alzheimer's disease, depression, anxiety, and epilepsy are disclosed. Acyloxyalkyl carbamate prodrugs of 3-aminopropylphosphinic acid and analogs thereof, which are suitable for oral administration and sustained release oral dosage forms are also disclosed.

      专利号:WO-2022246227-A1
      优先权日:2021-05-20
      标 题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

      专利号:US-10363247-B2
      优先权日:2015-08-18
      标 题:(S,E)-3-(6-aminopyridin-3-yl)-N-((5-(4-(3-fluoro-3-methylpyrrolidine-1-carbonyl)phenyl-7-(4-fluorophenyl)benzofuran-2-yl)methyl)acrylamide for the treatment of cancer
      发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM
      权利人:KARYOPHARM THERAPEUTICS INC
      摘要:The invention generally relates to substituted benzofuranyl compounds and, more particularly, to a compound represented by Structural Formula 1a: (I) or a pharmaceutically acceptable salt thereof. The invention also includes the synthesis and use of the compound of Structural Formula 1a, or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of diseases or disorder selected from cancer (e.g., lymphoma, such as mantle cell lymphoma), a neurodegenerative disease, an inflammatory diseases or an immune system disease (e.g., a T-Cell mediated autoimmune disease) in a subject in need thereof. The method comprises administering to a subject in need thereof a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, or a composition comprising a compound of the invention, or a pharmaceutically acceptable salt thereof.

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      ✅ COA系统入驻 | 共享模式

      主要参考文献


      1: Slimani K, Pirotais Y, Maris P, Abjean JP, Hurtaud-Pessel D. Liquid chromatography-tandem mass spectrometry method for the analysis of N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine, a biocidal disinfectant, in dairy products. Food Chem. 2018 Oct 1;262:168-177. doi: 10.1016/j.foodchem.2018.04.080. Epub 2018 Apr 25. 65(Pt 3):m115-7. doi: 10.1107/S0108270109002571. Epub 2009 Feb 7. 38(2):284-291. doi: 10.1002/jat.3523. Epub 2017 Sep 26. 59(Pt 12):m558-60. doi: 10.1107/s0108270103025836. Epub 2003 Nov 30.
      95:379-86. doi: 10.1016/j.chemosphere.2013.09.049. Epub 2013 Oct 11. 36(1):39-45. doi: 10.1016/j.nucmedbio.2008.10.010.
      7: Theoclitou ME, Aquila B, Block MH, Brassil PJ, Castriotta L, Code E, Collins MP, Davies AM, Deegan T, Ezhuthachan J, Filla S, Freed E, Hu H, Huszar D, Jayaraman M, Lawson D, Lewis PM, Nadella MV, Oza V, Padmanilayam M, Pontz T, Ronco L, Russell D, Whitston D, Zheng X. Discovery of (+)-N-(3-aminopropyl)-N-[1 -(5-benzyl-3-methyl-4-oxo-[1,2]thiazolo[5,4-d]pyrimidin-6-yl)-2-methylpropyl]-4- methylbenzamide (AZD4877), a kinesin spindle protein inhibitor and potential anticancer agent. J Med Chem. 2011 Oct 13;54(19):6734-50. doi: 10.1021/jm200629m. Epub 2011 Sep 7. 85(3):207-13. doi: 10.1254/jjp.85.207. 37(3):243-252. doi: 10.1002/jat.3351. Epub 2016 Jun 13. 32(1):547-563. doi: 10.1080/14756366.2016.1268608.

      合成参考文献


      摘要:Scientia Pharmaceutica., 37(185), 1969
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