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5-(benzyloxy)adamantan-2-one | 167856-60-2

中文名称
——
中文别名
——
英文名称
5-(benzyloxy)adamantan-2-one
英文别名
5-benzyloxyadamantan-2-one;5-phenylmethoxyadamantan-2-one
5-(benzyloxy)adamantan-2-one化学式
CAS
167856-60-2
化学式
C17H20O2
mdl
——
分子量
256.345
InChiKey
XAERWAGZMUEEOG-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

物化性质

  • 沸点:
    380.0±35.0 °C(Predicted)
  • 密度:
    1.16±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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

反应信息

  • 作为反应物:
    描述:
    5-(benzyloxy)adamantan-2-one 在 sodium tetrahydroborate 作用下, 以 乙醇 为溶剂, 反应 0.25h, 生成 5-benzyloxyadamantan-2-ol
    参考文献:
    名称:
    EP2172453
    摘要:
    公开号:
  • 作为产物:
    描述:
    溴甲苯四丁基碘化铵 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 16.75h, 以77%的产率得到5-(benzyloxy)adamantan-2-one
    参考文献:
    名称:
    WO2007/113634
    摘要:
    公开号:
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文献信息

  • Dipeptidyl peptidase IV inhibitors and processes for their preparation and pharmaceutical compositions containing them
    申请人:Matrix Laboratories Ltd.
    公开号:US07985759B2
    公开(公告)日:2011-07-26
    The present invention relates to novel compounds representated by formula (I), where R, R1, R2, R3, X, Y, m, n are as defined. The present invention relates to compounds of the general formula I their derivatives, their analogs, their tautomeric forms, their stereoisomers, their diastereomers, their bioisosteres, their polymorphs, their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them which are predominantly dipeptidyl peptidase IV inhibitors. The present invention also relates to the processes for the preparation of novel compounds of formula (I) and their use in treating type II diabetes and diabetic complications thereof and also for treating dislipidemia, hypercholesterolemia, obesity and hyperglycemia.
    本发明涉及由式(I)表示的新化合物,其中R,R1,R2,R3,X,Y,m,n的定义如下。本发明涉及通式I的化合物及其衍生物,类似物,互变异构体,立体异构体,对映异构体,生物等价物,多晶形,其药学上可接受的盐和包含它们的药学上可接受的组合物,这些化合物主要是二肽基肽酶IV抑制剂。本发明还涉及制备式(I)的新化合物的过程及其在治疗II型糖尿病及其并发症以及治疗血脂异常,高胆固醇血症,肥胖症和高血糖方面的用途。
  • NOVEL DIPEPTIDYL PEPTIDASE IV INHIBITORS AND PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:Gopalan Balasubramanian
    公开号:US20100160302A1
    公开(公告)日:2010-06-24
    The present invention relates to novel compounds representated by formula (I), where R, R1, R2, R3, X, Y, m, n are as defined. The present invention relates to compounds of the general formula I their derivatives, their analogs, their tautomeric forms, their stereoisomers, their diastereomers, their bioisosteres, their polymorphs, their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them which are predominantly dipeptidyl peptidase IV inhibitors. The present invention also relates to the processes for the preparation of novel compounds of formula (I) and their use in treating type II diabetes and diabetic complications thereof and also for treating dislipidemia, hypercholesterolemia, obesity and hyperglycemia.
    本发明涉及由式(I)所代表的新化合物,其中R,R1,R2,R3,X,Y,m,n如定义所示。本发明涉及通式I化合物及其衍生物、类似物、互变异构体、立体异构体、对映异构体、生物等构体、多晶型、其药学上可接受的盐和包含它们的药学上可接受的组合物,这些化合物主要是二肽基肽酶IV抑制剂。本发明还涉及制备式(I)的新化合物的过程,以及它们在治疗II型糖尿病及其并发症以及治疗血脂异常、高胆固醇血症、肥胖症和高血糖方面的应用。
  • Compound having 11β-HSD1 inhibitory activity
    申请人:Taisho Pharmaceutical Co., Ltd
    公开号:US08222417B2
    公开(公告)日:2012-07-17
    The present invention provides compounds having excellent 11β-HSD1 inhibitory activity. A compound represented by the following formula (I): [wherein X1 represents an oxygen atom, or the formula —(CR11R12)p—, etc., Y1 represents a hydrogen atom, a hydroxyl group, etc., Z1 represents an oxygen atom or the formula —(NR14)—, R1 represents a hydrogen atom, a halogen atom, a cyano group, a C1-4 alkyl group, a C1-4 alkyl group substituted with 1 to 3 halogen atoms, a C1-4 alkoxy group, a C1-4 alkoxycarbonyl group, a carboxyl group, a carbamoyl group, or an amino group, and m represents an integer of 1 or 2, and R2 represents a hydrogen atom or a C1-4 alkyl group, and n represents an integer of 1 or 2].
    本发明提供了具有优异11β-HSD1抑制活性的化合物。一种由以下式子(I)表示的化合物:[其中X1表示氧原子,或者式子—(CR11R12)p—等,Y1表示氢原子,羟基等,Z1表示氧原子或式子—(NR14)—,R1表示氢原子,卤素原子,氰基,C1-4烷基,1至3个卤素原子取代的C1-4烷基,C1-4烷氧基,C1-4烷氧羰基,羧基,氨基或氨基甲酰基,m表示1或2的整数,R2表示氢原子或C1-4烷基,n表示1或2的整数]。
  • COMPOUND HAVING 11BETA-HSD1 INHIBITORY ACTIVITY
    申请人:Suzuki Ryo
    公开号:US20100179325A1
    公开(公告)日:2010-07-15
    The present invention provides compounds having excellent 11β-HSD1 inhibitory activity. A compound represented by the following formula (I): [wherein X 1 represents an oxygen atom, or the formula —(CR 11 R 12 ) p —, etc., Y 1 represents a hydrogen atom, a hydroxyl group, etc., Z 1 represents an oxygen atom or the formula —(NR 14 )—, R 1 represents a hydrogen atom, a halogen atom, a cyano group, a C 1-4 alkyl group, a C 1-4 alkyl group substituted with 1 to 3 halogen atoms, a C 1-4 alkoxy group, a C 1-4 alkoxycarbonyl group, a carboxyl group, a carbamoyl group, or an amino group, and m represents an integer of 1 or 2, and R 2 represents a hydrogen atom or a C 1-4 alkyl group, and n represents an integer of 1 or 2].
    本发明提供了具有优异的11β-HSD1抑制活性的化合物。其中一种化合物的结构式为(I):[其中,X1表示氧原子,或者公式—(CR11R12)p—等;Y1表示氢原子,羟基等;Z1表示氧原子或者公式—(NR14)—等;R1表示氢原子,卤素原子,氰基,C1-4烷基,1至3个卤素原子取代的C1-4烷基,C1-4烷氧基,C1-4烷氧羰基,羧基,氨基或者氨基取代的羰基;m表示1或2的整数;R2表示氢原子或者C1-4烷基;n表示1或2的整数。]
  • COMPOUND HAVING 11 ß-HSD1 INHIBITORY ACTIVITY
    申请人:Taisho Pharmaceutical Co. Ltd.
    公开号:EP2172453A1
    公开(公告)日:2010-04-07
    The present invention provides compounds having excellent 11β-HSD1 inhibitory activity. A compound represented by the following formula (I): [wherein X1 represents an oxygen atom, or the formula -(CR11R12)p-, etc., Y1 represents a hydrogen atom, a hydroxyl group, etc., Z1 represents an oxygen atom or the formula -(NR14)-, R1 represents a hydrogen atom, a halogen atom, a cyano group, a C1-4 alkyl group, a C1-4 alkyl group substituted with 1 to 3 halogen atoms, a C1-4 alkoxy group, a C1-4 alkoxycarbonyl group, a carboxyl group, a carbamoyl group, or an amino group, and m represents an integer of 1 or 2, and R2 represents a hydrogen atom or a C1-4 alkyl group, and n represents an integer of 1 or 2].
    本发明提供了具有优异 11β-HSD1 抑制活性的化合物。 由下式(I)代表的化合物: 其中 X1代表氧原子,或式-(CR11R12)p-等、 Y1 代表氢原子、羟基等、 Z1 代表氧原子或式-(NR14)-、 R1 代表氢原子、卤素原子、氰基、C1-4 烷基、被 1 至 3 个卤素原子取代的 C1-4 烷基、C1-4 烷氧基、C1-4 烷氧羰基、羧基、氨基甲酰基或氨基,且 m 代表 1 或 2 的整数,且 R2 代表氢原子或 C1-4 烷基,n 代表 1 或 2 的整数]。
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