CAS: 6882-74-2; 4,5,6,7-Tetrahydro-3H-Imidazo[4,5-C]Pyridine

该化合物是一种环环环系统结合的七环化合物,该结构是制药和有机合成的多用途中间体,特别是在开发生物活性分子方面,其硬性双环框架加强了药用化学应用中的结合性,使其对设计酶抑制剂和受体调节器很有价值.该化合物的稳定性和合成可及性进一步有助于其建造复杂的脚架的用途.其氮富含结构还允许多处地点的功能化,从而能够对有针对性的研究应用进行量身定制的修改.该化合物通常用于合成CNS活性剂和其他治疗对象.

结构式图片

相似化合物

62002-31-7 1202800-68-7 879668-17-4

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CAS号109-87-5 甲缩醛 | CAS号51-45-6 组胺 | CAS号64403-25-4 4,5,6,7-tetrahy...

合成工艺路线路线简述

    📜Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于芴体系中,化学反应生成 4,5,6,7-四氢-1H-咪唑并[4,5-C]吡啶
    参考文献:Neuberger,Biochemical Journal,1944,Vol. 38,P. 309,314
    标题:Neuberger,Biochemical Journal,1944,Vol. 38,P. 309,314

    海关参考信息

    专利信息


    专利号:US-7138526-B1
    优先权日:1999-06-15
    标 题 :Solid phase synthesis of n,n-disubstituted diazacycloalkylcarboxy derivatives
    发明人:HERPIN TIMOTHY F; MORTON GEORGE C; SALVINO JOSEPH M
    权利人:AVENTIS PHARMA INC
    摘要:A method for the solid phase synthesis of N,N-disubstituted diazacycloalkylcarboxy derivatives of general formula (I) and (II) is claimed. Examples include piperazine-2-carboxamide. The method is applicable to the synthesis or large combinatorial libraries

    专利号:US-6127515-A
    优先权日:1997-11-18
    标 题:Functionalized resin for the synthesis of amides and peptides
    发明人:MANFRE FRANCO; VANASSE BENOIT J; LABAUDINIERE RICHARD F; MORTON GEORGE C
    权利人:AVENTIS PHARM PROD INC
    摘要:This invention is directed to a functionalized amino resin of formula ##STR1## wherein S is a solid support; R is H or alkyl; A is ##STR2## Y is OH or OCOR 1 ; and R 1 is aliphatic or aromatic which is useful for the solid phase synthesis of amides, peptides and hydroxamic acids.

    专利号:US-6133409-A
    优先权日:1996-12-19
    标 题:Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds
    发明人:SALVINO JOSEPH M; MORTON GEORGE C; MASON HELEN J; LABAUDINIERE RICHARD F
    权利人:AVENTIS PHARM PROD INC
    摘要:This invention is directed to a process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and alpha , beta -unsaturated carboxylic acid and aldehyde compounds and to polymeric hydroxylamine resin compounds useful therefor.

    专利号:US-6710208-B2
    优先权日:1996-12-19
    标题 :Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and α,β-unsaturated carboxylic acid and aldehyde compounds
    发明人:SALVINO JOSEPH M; MORTON GEORGE C; MASON HELEN J; LABAUDINIERE RICHARD F
    权利人:AVENTIS PHARMA INC
    摘要:This invention is directed to a process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and α,β-unsaturated carboxylic acid and aldehyde compounds and to polymeric hydroxylamine resin compounds useful therefor.

    专利号:US-8653282-B2
    优先权日:2007-10-18
    标 题:Preparation of dihydrothieno [3,2-D] pyrimidines and intermediates used therein
    发明人:FRUTOS ROGELIO; KRISHNAMURTHY DHILEEPKUMAR; MULDER JASON ALAN; RODRIGUEZ SONIA; SENANAYAKE CHRIS HUGH; TAMPONE THOMAS G
    权利人:FRUTOS ROGELIO; KRISHNAMURTHY DHILEEPKUMAR; MULDER JASON ALAN; RODRIGUEZ SONIA; SENANAYAKE CHRIS HUGH; TAMPONE THOMAS G; BOEHRINGER INGELHEIM INT
    摘要:The invention relates to improved methods of preparing dihydrothienopyrimidines of formula 1, and intermediates thereof, (I) wherein X is SO or SO 2 , preferably SO, and wherein R A , R 1 , R 2 , R 3 , R 4 and R 5 have the meanings given in the description. The methods according to this invention are more suitable for large-scale synthesis of said compounds than prior methods because the new synthetic process avoids distillation and chromatographic purification between steps and results in a higher overall yield of the desired product.

    专利号:US-12336981-B2
    优先权日:2010-09-03
    标题 :Compounds and compositions for the inhibition of NAMPT
    发明人:BAIR KENNETH W; BAUMEISTER TIMM R; BUCKMELTER ALEXANDRE J; CLODFELTER KARL H; DRAGOVICH Peter; GOSSELIN FRANCIS; HAN BINGSONG; LIN JIAN; REYNOLDS DOMINIC J; ROTH BRUCE; SMITH CHASE C; WANG ZHONGGUO; YUEN PO-WAI; ZHENG XIAOZHANG
    权利人:VALO HEALTH INC; GENENTECH INC
    摘要:The present invention relates to compounds and compositions for the inhibition of NAMPT, their synthesis, applications, and antidotes. An illustrative compound of the invention is shown below:

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1023/a:1012346021943
    摘要:Yutilov YM, Abramyants MG, Smolyar NN. Hydrogenation of 4-Phenylspinaceamines and Synthesis of 5-Benzylhistamines. Russian Journal of Organic Chemistry. 2001 Jan;37(1):119–24. doi: 10.1023/a:1012346021943.
    参考文献:10.1023/b:phac.0000048432.58231.b7
    摘要:Smolyar NN, Yutilov YM, Astashkina NV, Kochergin PM. Synthesis of 5-(N-Isopropylthiocarbamoyl)-2-azaspinaceamines: Analogs of Antisecretor Derivatives of Spinaceamine. Pharmaceutical Chemistry Journal. 2004 Jul;38(7):359–60. doi: 10.1023/b:phac.0000048432.58231.b7.
    参考文献:10.1007/7355_2014_40
    摘要:Junker A, Kokornaczyk AK, Strunz AK, Wünsch B. Selective and Dual Targeting of CCR2 and CCR5 Receptors: A Current Overview. 2014. In: Chemokines. : Springer International Publishing; 2014.
    参考文献:10.1007/bf00758316
    摘要:Vorob'ev SI, Islamov BI, Maevskii EI, Yarovaya SM, Grineva LP, Alekseeva GS, Telkova TN, Popova OY, Dombrovskii VA. Effects of oncotic agents as constituents of perfluorocarbon emulsions on the isolated heart. Pharmaceutical Chemistry Journal. 1989 Jan;23(1):51–4. doi: 10.1007/bf00758316.
    参考文献:10.1007/bf00758317
    摘要:Yutilov YM, Éilazyan OG, Khabarova TV, Boreko EI, Vladyko GV, Korobchenko LV. Synthesis and antiviral activity of spinaceamines. Pharmaceutical Chemistry Journal. 1989 Jan;23(1):54–7. doi: 10.1007/bf00758317.
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