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5-[(2S,4S)-2-(2,2-dimethylpropyl)piperidin-4-yl]-2,3-dihydro-1,2-oxazol-3-one | 1251841-49-2

中文名称
——
中文别名
——
英文名称
5-[(2S,4S)-2-(2,2-dimethylpropyl)piperidin-4-yl]-2,3-dihydro-1,2-oxazol-3-one
英文别名
5-((2S,4S)-2-Neopentylpiperidin-4-yl)isoxazol-3(2H)-one;(2S,4S)-5-(2-neopentylpiperidin-4-yl)isoxazol-3(2H)-one;5-[(2S,4S)-2-(2,2-dimethylpropyl)piperidin-4-yl]-1,2-oxazol-3-one
5-[(2S,4S)-2-(2,2-dimethylpropyl)piperidin-4-yl]-2,3-dihydro-1,2-oxazol-3-one化学式
CAS
1251841-49-2
化学式
C13H22N2O2
mdl
——
分子量
238.33
InChiKey
ORLPPUHANSFJCS-UWVGGRQHSA-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):
    2
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    50.4
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • ISOXAZOL-3(2H)-ONE ANALOGS AS THERAPEUTIC AGENTS
    申请人:BOSTRÖM Jonas
    公开号:US20100261755A1
    公开(公告)日:2010-10-14
    or a pharmaceutically suitable salt thereof, wherein, R 1 and R 2 independently are hydrogen, deuterium, aryl, hetero aryl, C1-C8 alkyl, optionally being substituted with one or more substituents independently being R 3 , R 3 is an aryl, hetero aryl, fluorine(s), a C1-C6 alkyl containing one or more fluorine, a C1-C6 alkyl containing one or more deuterium, a C1-C6 alkyl containing hydroxy, the aryl and heteroaryl optionally being substituted with one or more halogen, a fluorinated alkoxy, a fluorinated alkyl, a sulfonyl, one or more deuterium, a C1-6 alkyl, a C1-6 alkoxy, a nitrile, or R 3 is a C1-6 alkyl optionally substituted with one or more of the following groups: COOR4, OCOR4, CONR5R6, NR5COR6, OR4; wherein, R4 is a C1-10 alkyl optionally substituted with one or more fluorine, deuterium, alkoxy, arylcarboxylate, alkyl carboxylate; R5 and R6 are independently selected from hydrogen, alkyl or they may together form a 4-8 membered carbon ring; or R1 and R2 form a 3-10 membered carbon ring optionally comprising O or N and optionally substituted with a C1-10 alkyl or aryl, hetero aryl optionally substituted with R3.
    或其药学上适用的盐,其中, R1和R2独立地是氢、、芳基、杂环芳基、C1-C8烷基,可选地被一个或多个取代基取代,这些取代基独立地是R3, R3是芳基、杂环芳基、、含有一个或多个的C1-C6烷基、含有一个或多个的C1-C6烷基、含有羟基的C1-C6烷基,芳基和杂环芳基可选地被一个或多个卤素、代烷氧基、代烷基、磺酰基、一个或多个、C1-6烷基、C1-6烷氧基、腈取代, 或R3是一个C1-6烷基,可选地被以下一种或多种基团取代:COOR4、OCOR4、CONR5R6、NR5COR6、OR4; 其中,R4是一个C1-10烷基,可选地被一个或多个、烷氧基、芳基羧酸酯、烷基羧酸酯取代; R5和R6独立地选自氢、烷基,或它们可以共同形成一个4-8成员碳环; 或R1和R2形成一个3-10成员碳环,可选地包含O或N,并可选地被一个C1-10烷基或芳基、可选地被R3取代。
  • 3-(PIPERIDIN-4-YL)-ISOXAZOL-3(2H)-ONES FOR TREATMENT OF DERMATOLOGIC DISORDERS
    申请人:Emeriti Pharma AB
    公开号:EP3233189A1
    公开(公告)日:2017-10-25
  • 3-(PIPERIDIN-4-YL)-ISOXAZOL-3(OH)-ONES FOR TREATMENT OF DERMATOLOGIC DISORDERS
    申请人:Emeriti Pharma AB
    公开号:US20170360766A1
    公开(公告)日:2017-12-21
    Described are a group of isoxazol-3(2H)-one analogues and their use in topical formulations for the treatment and prophylaxis of dermatological disorders.
  • US8415378B2
    申请人:——
    公开号:US8415378B2
    公开(公告)日:2013-04-09
  • [EN] METHOD AND APPARATUS FOR PRODUCING HEAT ENERGY AND CARBON DIOXIDE<br/>[FR] PROCÉDÉ ET DISPOSITIF DE PRODUCTION D'ÉNERGIE THERMIQUE ET DE DIOXYDE DE CARBONE
    申请人:ASTRAZENECA AB
    公开号:WO2010117323A1
    公开(公告)日:2010-10-14
    Formula I or a pharmaceutically suitable salt thereof, wherein, R1 and R2 independently are hydrogen, deuterium, aryl, hetero aryl, C1-C8 alkyl, optionally being substituted with one or more substituents independently being R3, R3 is an aryl, hetero aryl, fluorine(s), a C1-C6 alkyl containing one or more fluorine, a C1-C6 alkyl containing one or more deuterium, a C1-C6 alkyl containing hydroxy, the aryl and heteroaryl optionally being substituted with one or more halogen, a fluorinated alkoxy, a fluorinated alkyl, a sulfonyl, one or more deuterium, a C1-6 alkyl, a C1-6 alkoxy, a nitrile, or R3 is a C1-6 alkyl optionally substituted with one or more of the following groups: COOR4, OCOR4, CONR5R6, NR5COR6, OR4; wherein, R4 is a C1-10 alkyl optionally substituted with one or more fluorine, deuterium, alkoxy, arylcarboxylate, alkyl carboxylate; R5 and R6 are independently selected from hydrogen, alkyl or they may together form a 4-8 membered carbon ring; or R1 and R2 form a 3-10 membered carbon ring optionally comprising O or N and optionally substituted with a C1-10 alkyl or aryl, hetero aryl optionally substituted with R3.
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