8-[4-(4,4-Dimethyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl]-1,4-dioxaspiro[4,5]decan-8-ol | 433211-84-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 8-[4-(4,4-Dimethyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl]-1,4-dioxaspiro[4,5]decan-8-ol
• 英文别名: 8-[4-(4,4-dimethyl-5H-1,3-oxazol-2-yl)phenyl]-1,4-dioxaspiro[4.5]decan-8-ol
• CAS: 433211-84-8
• 化学式: C₁₉H₂₅NO₄
• 分子量: 331.412
• InChiKey: NKRBVKINIIPLQB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  24
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  60.3
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  8-[4-(4,4-Dimethyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl]-1,4-dioxaspiro[4,5]decan-8-ol 在 吡啶 、 氯化亚砜 作用下， 以 二氯甲烷 为溶剂， 反应 3.25h， 生成 2-[4-(1,4-Dioxaspiro[4,5]dec-7-en-8-yl)phenyl]-4,4-dimethyl-4,5-dihydro-1,3-oxazole
  参考文献：
  名称：

  Cyclohexyl(alkyl)-propanolamines, preparation method and pharmaceutical compositions containing same

  摘要：

  本发明涉及以下公式（I）的化合物： 其中，A是公式（a）或（b）的基团； 其中，R表示氢或卤素原子、—S（O）z（C1-C4）烷基、—NHSO2（C1-C4）烷基、—SO2NH（C1-C4）烷基、—NHSO2苯基-(C1-C4)烷基或—NHSO2苯基，所述苯可能被卤素原子、(C1-C4)烷基或(C1-C4)氧烷基取代； R1表示氢原子或(C1-C4)烷基、—CO（C1-C4）烷基、苯基-(C1-C4)烷基或—CO苯基，所述苯也可能被卤素原子或(C1-C4)氧烷基取代； R2是氢原子或—SO2（C1-C4）烷基、—SO2苯基-(C1-C4)烷基或—SO2苯基； X完成5至8个原子的环，该环饱和或不饱和，可能被一个或两个(C1-C4)烷基取代，并带有一个或两个羰基基团； n，m和z独立地为0，1或2； R3表示氢或卤素原子、(C1-C6)烷基、(C1-C4)氧烷基、—COO（C1-C4）烷基、—CO（C1-C4）烷基、—NHSO2（C1-C4）烷基、—NHSO2苯基-(C1-C4)烷基、—NO2、—CN、—CONR4R5、—COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基； R4和R5独立地表示氢原子、苯基、(C1-C4)烷基或苯基-(C1-C4)烷基，或R4和R5与它们所连接的氮原子可以总共形成5至7个原子的环；以及其盐或溶剂化物、含有它们的制药组合物、制备它们的过程和该过程中的中间体。

  公开号：

  US20040053916A1
• 作为产物：
  描述：

  1,4-环己二酮单乙二醇缩酮 、 2-(4-溴苯基)-4,4-二甲基-4,5-二氢噁唑 在 magnesium 作用下， 以 四氢呋喃 为溶剂， 反应 5.0h， 生成 8-[4-(4,4-Dimethyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl]-1,4-dioxaspiro[4,5]decan-8-ol
  参考文献：
  名称：

  Cyclohexyl(alkyl)-propanolamines, preparation method and pharmaceutical compositions containing same

  摘要：

  本发明涉及以下公式（I）的化合物： 其中，A是公式（a）或（b）的基团； 其中，R表示氢或卤素原子、—S（O）z（C1-C4）烷基、—NHSO2（C1-C4）烷基、—SO2NH（C1-C4）烷基、—NHSO2苯基-(C1-C4)烷基或—NHSO2苯基，所述苯可能被卤素原子、(C1-C4)烷基或(C1-C4)氧烷基取代； R1表示氢原子或(C1-C4)烷基、—CO（C1-C4）烷基、苯基-(C1-C4)烷基或—CO苯基，所述苯也可能被卤素原子或(C1-C4)氧烷基取代； R2是氢原子或—SO2（C1-C4）烷基、—SO2苯基-(C1-C4)烷基或—SO2苯基； X完成5至8个原子的环，该环饱和或不饱和，可能被一个或两个(C1-C4)烷基取代，并带有一个或两个羰基基团； n，m和z独立地为0，1或2； R3表示氢或卤素原子、(C1-C6)烷基、(C1-C4)氧烷基、—COO（C1-C4）烷基、—CO（C1-C4）烷基、—NHSO2（C1-C4）烷基、—NHSO2苯基-(C1-C4)烷基、—NO2、—CN、—CONR4R5、—COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基； R4和R5独立地表示氢原子、苯基、(C1-C4)烷基或苯基-(C1-C4)烷基，或R4和R5与它们所连接的氮原子可以总共形成5至7个原子的环；以及其盐或溶剂化物、含有它们的制药组合物、制备它们的过程和该过程中的中间体。

  公开号：

  US20040053916A1

文献信息

• [EN] CYCLOHEXYL(ALKYL)-PROPANOLAMINES, PREPARATION METHOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME<br/>[FR] CYCLOHEXYL(ALKYL)-PROPANOLAMINES, LEUR PREPARATION ET COMPOSITIONS PHARMACEUTIQUES EN CONTENANT
  申请人：SANOFI SYNTHELABO

  公开号：WO2002044139A1

  公开（公告）日：2002-06-06

  La présente invention concerne les composés formule (I), dans laquelle A est un groupe de formule (a) ou (b) ainsi que leurs sels ou solvates, les compositions pharmaceutiques les contenant, un procédé pour leur préparation et des intermédiaires dans ce procécé. Les composés de formule (I) peuvent être indiqués dans le traitement des maladies gastro-intestinales telles que les maladies inflammatoires de l'intestin telles que le syndrôme du colon irritable (IBD), comme modulateurs de la motricité intestinale, comme lipolytiques, agents anti-obésité, anti-diabétiques, psychotropes, anti-glaucomateux, cicatrisants, anti-dépresseurs, comme inhib iteur des contractions utérines, comme tocolytiques pour prévenir ou retarder les accouchements précoces, pour le traitement et/ou la prophylaxie de la dysménorrhée. En outre les composés de formule (I) peuvent être utilisés dans le traitement de certaines maladies du système nerveux central, telle que par exemple la dépression, ainsi que de certains troubles du système urinaire tel que l'incontinence urinaire.

  本发明涉及具有式(I)的化合物，其中A是式(a)或(b)的基团，以及它们的盐或溶剂，包含它们的药物组合物，制备它们的方法以及该方法中的中间体。式(I)的化合物可用于治疗胃肠疾病，如炎症性肠病（IBD），作为肠动力调节剂，脂肪分解剂，抗肥胖剂，抗糖尿病剂，精神药物，抗青光眼剂，愈合剂，抗抑郁剂，作为子宫收缩抑制剂，作为止早产的止痛剂，用于治疗和/或预防痛经。此外，式(I)的化合物可用于治疗某些中枢神经系统疾病，例如抑郁症，以及某些泌尿系统疾病，如尿失禁。
• CYCLOHEXYL(ALKYL)PROPANOLAMINES, PREPARATION METHOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
  申请人：Bovy Philippe R.

  公开号：US20080261949A1

  公开（公告）日：2008-10-23

  The present invention relates to the compounds of formula (I): in which A is a group of formula (a) or (b) in which R represents a hydrogen or halogen atom, an —S(O) z (C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —SO 2 NH(C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl group or an —NHSO 2 phenyl group, said phenyl possibly being substituted with a halogen atom, with a (C 1 -C 4 )alkyl group or with a (C 1 -C 4 )alkoxy group; R 1 represents a hydrogen atom or a (C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, a phenyl-(C 1 -C 4 )alkyl group or a —COphenyl group, said phenyl also possibly being substituted with a halogen atom or with a (C 1 -C 4 )alkoxy group; R 2 is a hydrogen atom or an —SO 2 (C 1 -C 4 )alkyl group, an —SO 2 phenyl-(C 1 -C 4 )alkyl group or an —SO 2 phenyl group; X completes a ring of 5 to 8 atoms, said ring being saturated or unsaturated, possibly being substituted with one or two (C 1 -C 4 )alkyl groups and bearing one or two carbonyl groups; n, m and z are, independently, 0, 1 or 2; R 3 represents a hydrogen or halogen atom, a (C 1 -C 6 )alkyl group, a (C 1 -C 4 )alkoxy group, a —COO(C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl groups, —NO 2 , —CN, —CONR 4 R 5 , —COOH, or a 4,5-dihydro-1,3-oxazol-2-yl or 4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl group; R 4 and R 5 represent, independently, a hydrogen atom, a phenyl, a (C 1 -C 4 )alkyl group or a phenyl-(C 1 -C 4 )alkyl group or R 4 and R 5 with the nitrogen atom to which they are attached, may form a ring of 5 to 7 atoms in total; and to the salts or solvates thereof, to the pharmaceutical compositions containing them, to a process for the preparation thereof and to intermediates in this process.

  本发明涉及公式（I）的化合物： 其中A是公式（a）或（b）的基团： 其中R表示氢或卤素原子，-S（O）z（C1-C4）烷基，-NHSO2（C1-C4）烷基，-SO2NH（C1-C4）烷基，-NHSO2苯基-（C1-C4）烷基或-NHSO2苯基，所述苯基可能被卤素原子，（C1-C4）烷基或（C1-C4）氧烷基取代； R1表示氢原子或（C1-C4）烷基，-CO（C1-C4）烷基，苯基-（C1-C4）烷基或-CO苯基，所述苯基也可能被卤素原子或（C1-C4）氧烷基取代； R2是氢原子或-SO2（C1-C4）烷基，-SO2苯基-（C1-C4）烷基或-SO2苯基； X完成由5到8个原子组成的环，该环饱和或不饱和，可能被一个或两个（C1-C4）烷基取代，并带有一个或两个羰基基团； n，m和z独立地为0、1或2； R3表示氢或卤素原子，（C1-C6）烷基，（C1-C4）氧烷基，-COO（C1-C4）烷基，-CO（C1-C4）烷基，-NHSO2（C1-C4）烷基，-NHSO2苯基-（C1-C4）烷基，-NO2，-CN，-CONR4R5，-COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基； R4和R5独立地表示氢原子，苯基，（C1-C4）烷基或苯基-（C1-C4）烷基，或R4和R5与它们附着的氮原子一起可以形成总共5到7个原子的环；以及其盐或溶剂，含有它们的制药组合物，制备过程和其中间体的本发明。
• Cyclohexyl(alkyl)propanolamines, Preparation Method and Pharmaceutical Compositions Containing Same
  申请人：BOVY R. Philippe

  公开号：US20070015745A1

  公开（公告）日：2007-01-18

  The present invention relates to the compounds of formula (I): in which A is a group of formula (a) or (b) in which R represents a hydrogen or halogen atom, an —S(O) z (C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —SO 2 NH(C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl group or an —NHSO 2 phenyl group, said phenyl possibly being substituted with a halogen atom, with a (C 1 -C 4 )alkyl group or with a (C 1 -C 4 )alkoxy group; R 1 represents a hydrogen atom or a (C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, a phenyl-(C 1 -C 4 )alkyl group or a —CO—phenyl group, said phenyl also possibly being substituted with a halogen atom or with a (C 1 -C 4 )alkoxy group; R 2 is a hydrogen atom or an —SO 2 (C 1 -C 4 )alkyl group, an —SO 2 phenyl-(C 1 -C 4 )alkyl group or an —SO 2 phenyl group; X completes a ring of 5 to 8 atoms, said ring being saturated or unsaturated, possibly being substituted with one or two (C 1 -C 4 )alkyl groups and bearing one or two carbonyl groups; n, m and z are, independently, 0, 1 or 2; R 3 represents a hydrogen or halogen atom, a (C 1 -C 6 )alkyl group, a (C 1 -C 4 )alkoxy group, a —COO(C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl groups, —NO 2 , —CN, —CONR 4 R 5 , —COOH, or a 4,5-dihydro-1,3-oxazol-2-yl or 4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl group; R4 and R 5 represent, independently, a hydrogen atom, a phenyl, a (C 1 -C 4 )alkyl group or a phenyl-(C 1 -C 4 )alkyl group or R 4 and R 5 with the nitrogen atom to which they are attached, may form a ring of 5 to 7 atoms in total; and to the salts or solvates thereof, to the pharmaceutical compositions containing them, to a process for the preparation thereof and to intermediates in this process.

  本发明涉及式(I)的化合物： 其中，A是式(a)或(b)的基团： 其中，R代表氢或卤素原子，-S(O)z(C1-C4)烷基，-NHSO2(C1-C4)烷基，-SO2NH(C1-C4)烷基，-NHSO2苯基-(C1-C4)烷基或-NHSO2苯基，所述苯可能被卤素原子，(C1-C4)烷基或(C1-C4)氧代基取代；R1代表氢原子或(C1-C4)烷基，-CO(C1-C4)烷基，苯基-(C1-C4)烷基或-CO-苯基，所述苯也可能被卤素原子或(C1-C4)氧代基取代；R2是氢原子或-SO2(C1-C4)烷基，-SO2苯基-(C1-C4)烷基或-SO2苯基；X完成一个由5到8个原子组成的环，该环饱和或不饱和，可能被一个或两个(C1-C4)烷基取代，并带有一个或两个羰基基团；n，m和z独立地为0，1或2；R3代表氢或卤素原子，(C1-C6)烷基，(C1-C4)氧代基，-COO(C1-C4)烷基，-CO(C1-C4)烷基，-NHSO2(C1-C4)烷基，-NHSO2苯基-(C1-C4)烷基，-NO2，-CN，-CONR4R5，-COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基；R4和R5独立地代表氢原子，苯基，(C1-C4)烷基或苯基-(C1-C4)烷基，或R4和R5与它们所连接的氮原子可以总共形成一个由5到7个原子组成的环；以及它们的盐或溶剂合物，含有它们的制药组合物，制备它们的过程以及在该过程中的中间体。
• Oxophenyl-Cyclohexyl-Propanolamine Derivatives, Production And Use Thereof In Therapeutics
  申请人：BOVY Philippe R.

  公开号：US20100075986A1

  公开（公告）日：2010-03-25

  The invention relates to the compounds of general formula (I) where R 1 represents H, a (C1-C4)alkyl, —CO(C1-C4)alkyl, (C1-C4)alkylphenyl or —CO-phenyl group, said phenyl being optionally substituted, R 2 represents H, a halogen atom, an —S(O) z R 3 , —NHSO 2 R 3 , —NHSO 2 -phenyl or —NHSO 2 —(C1-C4)alkylphenyl group where z is equal to 0, 1 or 2 and where R 3 represents a (C1-C4)alkyl group, said phenyl being optionally substituted; A is chosen from where n is equal to 0, 1 or 2, R 4 and R 5 represent H, a (C1-C4)alkyl, hydroxyl, cyano, phenyl, benzyl, piperidyl, —CONH 2 , —CO-phenyl, —COOR 3 , —CH(phenyl) (OH) and —C(phenyl) 2 (OH) group, or R 4 and R 5 form together an optionally substituted 6-membered aromatic ring, R 6 represents H, a (C1-C4)alkyl, phenyl or benzyl group, and B represents a 5- or 6-membered nitrogen-containing heterocycle or homocycle optionally fused with a phenyl group or optionally substituted; their addition salts; their method of preparation and their therapeutic application.

  本发明涉及一般式（I）化合物，其中R1代表H，（C1-C4）烷基，-CO（C1-C4）烷基，（C1-C4）烷基苯基或-CO-苯基，所述苯基可选地被取代，R2代表H，卤素原子，-S（O）zR3，-NHSO2R3，-NHSO2-苯基或-NHSO2-（C1-C4）烷基苯基，其中z等于0、1或2，R3代表（C1-C4）烷基，所述苯基可选地被取代；A从下列中选择：其中n等于0、1或2，R4和R5代表H，（C1-C4）烷基，羟基，氰基，苯基，苄基，哌啶基，-CONH2，-CO-苯基，-COOR3，-CH（苯基）（OH）和-C（苯基）2（OH）基，或R4和R5共同形成一个可选取代的6元芳香环，R6代表H，（C1-C4）烷基，苯基或苄基，B代表5-或6-成员的含氮杂环或同环，可选地与苯基融合或可选地取代；它们的加成盐；它们的制备方法和它们的治疗应用。
• Cyclohexyl(alkyl)propanolamines, preparation method and pharmaceutical compositions containing same
  申请人：Sanofi-Aventis

  公开号：US07419974B2

  公开（公告）日：2008-09-02

  The present invention relates to the compounds of formula (I): in which A is a group of formula (a) or (b) in which R represents a hydrogen or halogen atom, an —S(O)z(C1-C4)alkyl group, an —NHSO2(C1-C4)alkyl group, an —SO2NH(C1-C4)alkyl group, an —NHSO2phenyl-(C1-C4)alkyl group or an —NHSO2phenyl group, said phenyl possibly being substituted with a halogen atom, with a (C1-C4)alkyl group or with a (C1-C4)alkoxy group; R1 represents a hydrogen atom or a (C1-C4)alkyl group, a —CO(C1-C4)alkyl group, a phenyl-(C1-C4)alkyl group or a —COphenyl group, said phenyl also possibly being substituted with a halogen atom or with a (C1-C4)alkoxy group; R2 is a hydrogen atom or an —SO2(C1-C4)alkyl group, an —SO2phenyl-(C1-C4)alkyl group or an —SO2phenyl group; X completes a ring of 5 to 8 atoms, said ring being saturated or unsaturated, possibly being substituted with one or two (C1-C4)alkyl groups and bearing one or two carbonyl groups; n, m and z are, independently, 0, 1 or 2; R3 represents a hydrogen or halogen atom, a (C1-C6)alkyl group, a (C1-C4)alkoxy group, a —COO(C1-C4)alkyl group, a —CO(C1-C4)alkyl group, an —NHSO2(C1-C4)alkyl group, an —NHSO2phenyl-(C1-C4)alkyl groups, —NO2, —CN, —CONR4R5, —COOH, or a 4,5-dihydro-1,3-oxazol-2-yl or 4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl group; R4 and R5 represent, independently, a hydrogen atom, a phenyl, a (C1-C4)alkyl group or a phenyl-(C1-C4)alkyl group or R4 and R5 with the nitrogen atom to which they are attached, may form a ring of 5 to 7 atoms in total; and to the salts or solvates thereof, to the pharmaceutical compositions containing them, to a process for the preparation thereof and to intermediates in this process.

  本发明涉及式(I)的化合物： 其中，A是式(a)或(b)的基团，其中R代表氢原子或卤素原子，-S(O)z(C1-C4)烷基，-NHSO2(C1-C4)烷基，-SO2NH(C1-C4)烷基，-NHSO2苯基-(C1-C4)烷基或-NHSO2苯基，所述苯基可能被卤素原子、(C1-C4)烷基或(C1-C4)烷氧基取代；R1代表氢原子或(C1-C4)烷基，-CO(C1-C4)烷基，苯基-(C1-C4)烷基或-CO苯基，所述苯基也可能被卤素原子或(C1-C4)烷氧基取代；R2是氢原子或-SO2(C1-C4)烷基，-SO2苯基-(C1-C4)烷基或-SO2苯基；X完成5到8个原子的环，该环饱和或不饱和，可能被一个或两个(C1-C4)烷基取代，且带有一个或两个羰基；n、m和z分别为0、1或2；R3代表氢原子或卤素原子、(C1-C6)烷基、(C1-C4)烷氧基、-COO(C1-C4)烷基、-CO(C1-C4)烷基、-NHSO2(C1-C4)烷基、-NHSO2苯基-(C1-C4)烷基、-NO2、-CN、-CONR4R5、-COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基；R4和R5分别代表氢原子、苯基、(C1-C4)烷基或苯基-(C1-C4)烷基，或R4和R5与它们所连接的氮原子一起可以形成总共5到7个原子的环；以及其盐或溶剂，以及包含它们的制药组合物、制备它们的过程和该过程中的中间体。