(5-溴-2-甲基苯基)-(4-甲氧基苯基)甲酮 | 333361-13-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: (5-溴-2-甲基苯基)-(4-甲氧基苯基)甲酮
• 英文名称: 5-bromo-2-methyl-4'-methoxybenzophenone
• 英文别名: (5-Bromo-2-methyl-phenyl)-(4-methoxy-phenyl)-methanone；(5-Bromo-2-methylphenyl)(4-methoxyphenyl)methanone；(5-bromo-2-methylphenyl)-(4-methoxyphenyl)methanone
• CAS: 333361-13-0
• 化学式: C₁₅H₁₃BrO₂
• mdl: MFCD21508232
• 分子量: 305.171
• InChiKey: ZEDYNUOQIHWKIW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.133
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  草酰氯 、 5-溴-2-甲氧基苄氯 、 2-甲基-5-溴苯甲酸 在 AlCl₃ 盐酸 作用下， 以 二硫化碳 、 二氯甲烷 、 苯甲醚 、 N,N-二甲基甲酰胺 为溶剂， 生成 (5-溴-2-甲基苯基)-(4-甲氧基苯基)甲酮
  参考文献：
  名称：

  C-aryl glucoside SGLT2 inhibitors and method

  摘要：

  提供了一种用于治疗糖尿病及相关疾病的方法，使用化合物formula1的SGLT2抑制剂量，可以单独使用，也可以与一个或多个其他抗糖尿病药物或其他治疗药物组合使用。

  公开号：

  US20030114390A1

文献信息

• Processes for preparing of glucopyranosyl-substituted (ethynyl-benzyl)-benzene derivatives and intermediates thereof
  申请人：ECKHARDT Matthias

  公开号：US20070073046A1

  公开（公告）日：2007-03-29

  The present invention relates to processes for preparing the compounds of general formula I, wherein the groups R 1 , R 2 and R 3 are defined according to claim 1 and to intermediates of said processes.

  本发明涉及制备一般式I化合物的过程，其中基团R1、R2和R3根据权利要求1定义，并涉及所述过程的中间体。
• Glucopyranosyl-substituted benzyl-benzene derivatives, medicaments containing such compounds, their use and process for their manufacture
  申请人：Himmelsbach Frank

  公开号：US20070004648A1

  公开（公告）日：2007-01-04

  Glucopyranosyloxy-substituted benzyl-benzene derivatives of the general formula I where the groups groups R 1 , R 2 , R 3a , R 3b , R 4 , R 5 , R 6 , X and R 7a , R 7b , R 7c are defined according to claim 1, including the tautomers, the stereoisomers thereof, the mixtures thereof and the salts thereof. The compounds according to the invention are suitable for the treatment of metabolic disorders.

  根据权利要求1定义的通用公式I的葡萄糖吡喃氧基取代的苄基苯衍生物，包括基团R1、R2、R3a、R3b、R4、R5、R6、X以及R7a、R7b、R7c，包括互变异构体、立体异构体、它们的混合物以及它们的盐。根据发明的化合物适用于治疗代谢紊乱。
• C-aryl glucoside SGLT2 inhibitors and method
  申请人：——

  公开号：US20030114390A1

  公开（公告）日：2003-06-19

  A method is provided for treating diabetes and related diseases employing an SGLT2 inhibiting amount of a compound of the formula 1 alone or in combination with one or more other antidiabetic agent(s) or other therapeutic agent(s).

  提供了一种用于治疗糖尿病及相关疾病的方法，使用化合物formula1的SGLT2抑制剂量，可以单独使用，也可以与一个或多个其他抗糖尿病药物或其他治疗药物组合使用。
• Glucopyranosyl-substituted (heteroaryloxy-benzyl)-benzene derivatives, medicaments containing such compounds, their use and process for their manufacture
  申请人：Himmelsbach Frank

  公开号：US20060234953A1

  公开（公告）日：2006-10-19

  Glucopyranosyloxy-substituted (heteroaryloxy-benzyl)-benzene compounds of the general formula I where the groups R 1 to R 6 as well as R 7a , R 7b , R 7c are defined according to claim 1, including the tautomers, the stereoisomers thereof, the mixtures thereof and the salts thereof. The compounds according to the invention are suitable for the treatment of metabolic disorders.

  通式I的葡萄糖吡喃氧基取代的（杂环氧基苄基）-苯化合物，其中基团R1至R6以及R7a、R7b、R7c根据权利要求1定义，包括其互变异构体、立体异构体、混合物及其盐。本发明的化合物适用于治疗代谢性疾病。
• [EN] C-ARYL GLUCOSIDE SGLT2 INHIBITORS<br/>[FR] INHIBITEURS DE SGLT2 A BASE DE GLUCOSIDE C-ARYLE
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2001027128A1

  公开（公告）日：2001-04-19

  SGLT2 inhibiting compounds are provided having formula (I) where R?1, R2, and R2a¿ are independently hydrogen, OH, OR5, lower alkyl, CF¿3?, OCHF2, OCF3, SR?5i¿ or halogen, or two of R?1, R2 and R2a¿ together with the carbons to which they are attached can form an annelated five, six or seven membered carbocycle or heterocycle; R?3 and R4¿ are independently hydrogen, OH, OR5a, OAryl, OCH¿2?Aryl, lower alkyl, cycloalkyl, CF3, -OCHF2, -OCF3, halogen, -CN, -CO2R?5b, -CO¿2H, -COR6b, -CH(OH)R6c, -CH(OR?5h)R6d, -CONR6R6a¿, -NHCOR5c, -NHSO¿2R?5d, -NHSO¿2?Aryl, Aryl, -SR?5e, -SOR5f, SO¿2R5g, SO2Aryl, or a five, six or seven membered heterocycle, or R?3 and R4¿ together with the carbons to which they are attached form an annelated five, six or seven membered carbocycle or heterocycle; R?5, R5a, R5b, R5c, R5d, R5e, R5f, R5g, R5h, and R5I¿ are independently lower alkyl; R?6, R6a, R6b, R6c and R6d¿ are independently hydrogen, alkyl, aryl, alkylaryl or cycloalkyl, or R?6 and R6a¿ together with the nitrogen to which they are attached form an annelated five, six or seven membered heterocycle; A is O, S, NH, or (CH¿2?)n where n is 0 - 3. A method is also provided for treating diabetes and related diseases employing an SGLT2 inhibiting amount of the above compound alone or in combination with another antidiabetic agent or other therapeutic agent.

  提供具有公式（I）的SGLT2抑制化合物，其中R?1，R2和R2a¿独立地是氢，OH，OR5，低碳基，CF¿3？，OCHF2，OCF3，SR?5i¿或卤素，或者R?1，R2和R2a¿中的两个与它们附着的碳可以形成一个嵌环的五元，六元或七元碳环或杂环；R?3和R4¿独立地是氢，OH，OR5a，OAryl，OCH¿2？Aryl，低碳基，环烷基，CF3，-OCHF2，-OCF3，卤素，-CN，-CO2R?5b，-CO¿2H，-COR6b，-CH（OH）R6c，-CH（OR?5h）R6d，-CONR6R6a¿，-NHCOR5c，-NHSO¿2R?5d，-NHSO¿2？Aryl，芳基，-SR?5e，-SOR5f，SO¿2R5g，SO2Aryl或五元，六元或七元杂环，或R?3和R4¿与它们附着的碳形成一个嵌环的五元，六元或七元碳环或杂环；R?5，R5a，R5b，R5c，R5d，R5e，R5f，R5g，R5h和R5I¿独立地是低碳基；R?6，R6a，R6b，R6c和R6d¿独立地是氢，烷基，芳基，烷基芳基或环烷基，或者R?6和R6a¿与它们附着的氮一起形成一个嵌环的五元，六元或七元杂环；A是O，S，NH或（CH¿2？）n，其中n为0-3。还提供了一种使用上述化合物的SGLT2抑制量单独或与另一种抗糖尿病药物或其他治疗药物组合治疗糖尿病和相关疾病的方法。