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tert-butyl 4-(5-chloropyridin-2-yloxy)piperidine-1-carboxylate | 442199-12-4

中文名称
——
中文别名
——
英文名称
tert-butyl 4-(5-chloropyridin-2-yloxy)piperidine-1-carboxylate
英文别名
tert-butyl 4-[(5-chloro-2-pyridyl)oxy]-1-piperidinecarboxylate;t-butyl 4-[(5-chloropyridin-2-yl)oxy]piperidine-1-carboxylate;tert-butyl 4-(5-chloropyridin-2-yl)oxypiperidine-1-carboxylate
tert-butyl 4-(5-chloropyridin-2-yloxy)piperidine-1-carboxylate化学式
CAS
442199-12-4
化学式
C15H21ClN2O3
mdl
——
分子量
312.796
InChiKey
KYEQOMHKHDBCRP-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):
    3.2
  • 重原子数:
    21
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    51.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Peptide compounds
    申请人:——
    公开号:US20040097425A1
    公开(公告)日:2004-05-20
    The present invention relates to a compound of the formula (I)wherein R1 is benzofuranyl substituted by halogen, or styryl substituted by halogen; R2 is substituted hydroxy, substituted mercapto or substituted sulfonyl; and X is or pharmaceutically acceptable salts thereof. The compound (1) of the present invention and pharmaceutically acceptable salts thereof possess a strong inhibitory activity on the production of nitric oxide (NO), and are useful for prevention and/or treatment of NO-mediated diseases in human being and animals. 1
    本发明涉及一种化合物,其化学式为(I),其中R1为被卤素取代的苯并呋喃基或被卤素取代的苯乙烯基;R2为取代羟基、取代巯基或取代磺酰基;X为或其药用可接受盐。本发明的化合物(1)及其药用可接受盐对一氧化氮(NO)的产生具有强烈的抑制活性,并可用于预防和/或治疗人类和动物体内的NO介导的疾病。
  • HYDROXYQUINOXALINECARBOXAMIDE DERIVATIVE
    申请人:Motoki Kayoko
    公开号:US20110053933A1
    公开(公告)日:2011-03-03
    The present invention provides a novel hydroxyquinoxaline carboxamide derivative that is useful for preventing and/or treating blood coagulation disorders. A compound represented by formula (i), or a pharmacologically acceptable salt thereof: wherein, each of R 1 and R 2 independently represents a group such as a hydrogen atom or a halogen atom; R 3 represents a group such as a hydrogen atom; each of R 4 and R 5 independently represents a group such as a hydrogen atom, a halogen atom or a C 1-4 alkyl group; each of R 6 and R 7 independently represents a hydrogen atom or a C 1-4 alkyl group; X represents a group such as a C 3-10 cycloalkyl group, C 6-10 aryl group or a 5- to 10-membered heterocyclic group, which may be substituted with substituent(s) selected from substituent group α; Y represents a group such as —CO—, —O— or —NRa—, and Ra represents a group such as a hydrogen atom or a C 1-4 alkyl group.
    本发明提供了一种新型的羟基喹喔啉羧酰胺衍生物,可用于预防和/或治疗血液凝固障碍。该化合物由式(i)表示,或其药学上可接受的盐:其中,R1和R2各自独立地表示氢原子或卤素原子等基团;R3表示氢原子等基团;R4和R5各自独立地表示氢原子、卤素原子或C1-4烷基等基团;R6和R7各自独立地表示氢原子或C1-4烷基等基团;X表示C3-10环烷基、C6-10芳基或5-至10元杂环基等基团,该基团可以被选自取代基团α的取代基团所取代;Y表示—CO—、—O—或—NRa—等基团,其中Ra表示氢原子或C1-4烷基等基团。
  • SULFONYL PIPERIDINE DERIVATIVES AND THEIR USE FOR TREATING PROKINETICIN MEDIATED DISEASES
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US20150111922A1
    公开(公告)日:2015-04-23
    The present invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof: (I) in which m, n, W, X, Y, Z, R 1 , R 2 , R 3 and R 4 are as defined in the specification, for use in the treatment or prevention of a diseases o conition mediated by a prokineticin, such as psychiatric and neurological conditions.
    本发明提供了公式(I)的化合物及其药学上可接受的盐:(I)其中m、n、W、X、Y、Z、R1、R2、R3和R4如规范中所定义,用于治疗或预防由前动力素介导的疾病或情况,例如精神和神经疾病。
  • Sulfonyl piperidine derivatives and their use for treating prokineticin mediated diseases
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US10167273B2
    公开(公告)日:2019-01-01
    The present invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof in which q, R11, R12, R13 and R14 are as defined in the specification, for use in therapy.
    本发明提供了式 (I) 化合物及其药学上可接受的盐类 其中 q、R11、R12、R13 和 R14 如说明书中所定义,用于治疗。
  • EP2258697
    申请人:——
    公开号:——
    公开(公告)日:——
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