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1-isopropyl-3,3-dimethoxyyclopentanecarboxylate | 400770-74-3

中文名称
——
中文别名
——
英文名称
1-isopropyl-3,3-dimethoxyyclopentanecarboxylate
英文别名
1-isopropyl-3-oxocyclopentanecarboxylic acid;3-oxocyclopentane carboxylic acid;3-Oxo-1-isopropylcyclopentanecarboxylic acid;1-isopropyl-3-oxocyclopentylcarboxylic acid;3-oxo-1-propan-2-ylcyclopentane-1-carboxylic acid
1-isopropyl-3,3-dimethoxyyclopentanecarboxylate化学式
CAS
400770-74-3
化学式
C9H14O3
mdl
——
分子量
170.208
InChiKey
URZVRNBNUQBLCK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-isopropyl-3,3-dimethoxyyclopentanecarboxylate 在 palladium 10% on activated carbon 、 N,N-二甲基甲酰胺 4-二甲氨基吡啶草酰氯氢气三乙胺 作用下, 以 甲醇正己烷二氯甲烷异丙醇 为溶剂, 反应 10.75h, 生成 (1S)-1-异丙基-3-氧代环戊烷羧酸
    参考文献:
    名称:
    Benzoxazinyl-amidocyclopentyl-heterocyclic modulators of chemokine receptors
    摘要:
    环戊基化合物通过酰胺基团与苯并噁唑基团相连,利用苯并噁唑环的环氮原子,并进一步用杂环基团取代,这些化合物由式I表示: 用于调节CCR-2趋化因子受体,以预防或治疗炎症和免疫调节性疾病和疾病,过敏性疾病,包括过敏性鼻炎,皮炎,结膜炎和哮喘,以及类风湿性关节炎和动脉粥样硬化等自身免疫病理病变;以及包含这些化合物的药物组合物和这些化合物和组合物的使用。
    公开号:
    US20070238723A1
  • 作为产物:
    参考文献:
    名称:
    Alkylamino, arylamino, and sulfonamido cyclopentyl amide modulators of chemokine receptor activity
    摘要:
    公式(I)的化合物是化学趋化因子受体活性调节剂,对预防或治疗某些炎症和免疫调节性疾病和疾病、过敏性疾病、包括过敏性鼻炎、皮炎、结膜炎和哮喘等特应性疾病,以及风湿性关节炎和动脉粥样硬化等自身免疫病理学,以及包含这些化合物的药物组合物,以及这些化合物和组合物在涉及化学趋化因子受体的疾病的预防或治疗中的用途。
    公开号:
    US20070117797A1
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文献信息

  • Heterocyclic cyclopentyl tetrahydroisoquinoline and tetrahydropyridopyridine modulators of chemokine receptor activity
    申请人:Butora Gabor
    公开号:US20080081803A1
    公开(公告)日:2008-04-03
    The present invention is directed to compounds of the formula I: Wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , X, n and the broken lines are as defined herein which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.
    本发明涉及以下式I的化合物: 其中R1、R2、R3、R4、R5、R6、R7、R8、R9、X、n和虚线如本文所定义,这些化合物可用作趋化因子受体活性的调节剂。特别地,这些化合物可用作趋化因子受体CCR-2的调节剂。
  • Cyclopentyl modulators of chemokine receptor activity
    申请人:——
    公开号:US20020049222A1
    公开(公告)日:2002-04-25
    The present invention is directed to compounds of the formula I: 1 (wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and X are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.
    本发明涉及具有以下式I:1的化合物(其中R1、R2、R3、R4、R5、R6和X如本文中所定义),其可用作化学趋化因子受体活性的调节剂。特别是,这些化合物可用作化学趋化因子受体CCR-2的调节剂。
  • 2,6-Disubstituted piperiddines as modulators
    申请人:Yang Lihu
    公开号:US20070179158A1
    公开(公告)日:2007-08-02
    The present invention is further directed to compounds of formula (I): wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 16 , R 17 , R 18 , R 19 , R 20 , R 21 and R 22 are as defined herein) which are modulators of chemokine receptor activity and are useful in the prevention or treatment of certain inflammatory and immunoregulatory disorders and diseases, allergic diseases, atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and asthma, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which chemokine receptors are involved.
    本发明进一步涉及具有以下结构的化合物(I):其中R1、R2、R3、R4、R5、R6、R7、R8、R9、R10、R16、R17、R18、R19、R20、R21和R22如本文所定义),这些化合物是趋化因子受体活性的调节剂,并且在预防或治疗某些炎症和免疫调节性疾病、过敏性疾病、包括过敏性鼻炎、皮炎、结膜炎和哮喘等特应性疾病,以及风湿性关节炎和动脉粥样硬化等自身免疫病理学方面是有用的。本发明还涉及包含这些化合物的药物组合物以及这些化合物和组合物在预防或治疗涉及趋化因子受体的疾病中的用途。
  • Heterarylpiperidine modulators of chemokine receptor activity
    申请人:Goble D. Stephen
    公开号:US20050250781A1
    公开(公告)日:2005-11-10
    The present invention is directed to compounds of the formula (I): (wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 10 and n are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.
    本发明涉及以下式(I)的化合物:(其中R1,R2,R3,R4,R5,R6,R10和n在此定义),这些化合物可用作趋化因子受体活性的调节剂。特别地,这些化合物可用作趋化因子受体CCR-2的调节剂。
  • 2,6-disubstituted piperiddines as modulators
    申请人:Merck & Co., Inc.
    公开号:US07410961B2
    公开(公告)日:2008-08-12
    The present invention is further directed to compounds of formula (I): wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R16, R17, R18, R19, R20, R21 and R22 are as defined herein) which are modulators of chemokine receptor activity and are useful in the prevention or treatment of certain inflammatory and immunoregulatory disorders and diseases, allergic diseases, atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and asthma, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which chemokine receptors are involved.
    本发明进一步涉及式(I)的化合物:其中R1,R2,R3,R4,R5,R6,R7,R8,R9,R10,R16,R17,R18,R19,R20,R21和R22如本文所定义的那样,它们是趋化因子受体活性调节剂,并且在预防或治疗某些炎症和免疫调节性疾病和疾病,过敏性疾病,包括过敏性鼻炎,皮炎,结膜炎和哮喘,以及自身免疫病理,如类风湿关节炎和动脉粥样硬化方面有用。本发明还涉及包含这些化合物的制药组合物以及在涉及趋化因子受体的这些疾病的预防或治疗中使用这些化合物和组合物。
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