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1-(4-Benzylpiperazin-1-yl)-3-phenylpentane-2,4-dione | 167273-26-9

中文名称
——
中文别名
——
英文名称
1-(4-Benzylpiperazin-1-yl)-3-phenylpentane-2,4-dione
英文别名
——
1-(4-Benzylpiperazin-1-yl)-3-phenylpentane-2,4-dione化学式
CAS
167273-26-9
化学式
C22H26N2O2
mdl
——
分子量
350.461
InChiKey
GNQJYCNOXDQYRM-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):
    2.9
  • 重原子数:
    26
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    1-(4-Benzylpiperazin-1-yl)-3-phenylpentane-2,4-dione一水合肼 作用下, 以 甲醇 为溶剂, 反应 1.0h, 生成 1-benzyl-4-(5-methyl-4-phenyl-1H-pyrazol-3-ylmethyl)-piperazine
    参考文献:
    名称:
    Substituted pyrazoles as novel selective ligands for the human dopamine D 4 receptor
    摘要:
    Two novel series of 3-(heterocyclylmethyl)pyrazoles have been synthesised and evaluated as ligands for the human dopamine D-4 receptor. Compounds in series I (exemplified by 8k) have a phenyl ring joined to the 4-position of the pyrazole while those in series II (exemplified by 15j) have a 5-phenyl ring linked by a saturated chain to the 4-position of the pyrazole. Both series supplied compounds with excellent affinity for the human D-4 and good selectivity over other dopamine receptors. Excellent selectivity over calcium, sodium, and potassium ion channels was also achieved. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(98)00134-5
  • 作为产物:
    参考文献:
    名称:
    Substituted pyrazoles as novel selective ligands for the human dopamine D 4 receptor
    摘要:
    Two novel series of 3-(heterocyclylmethyl)pyrazoles have been synthesised and evaluated as ligands for the human dopamine D-4 receptor. Compounds in series I (exemplified by 8k) have a phenyl ring joined to the 4-position of the pyrazole while those in series II (exemplified by 15j) have a 5-phenyl ring linked by a saturated chain to the 4-position of the pyrazole. Both series supplied compounds with excellent affinity for the human D-4 and good selectivity over other dopamine receptors. Excellent selectivity over calcium, sodium, and potassium ion channels was also achieved. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(98)00134-5
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文献信息

  • [EN] ISOXAZOLE AND PYRAZOLE DERIVATIVES AS DOPAMINE RECEPTOR SUBTYPE LIGANDS<br/>[FR] DERIVES D'ISOXAZOLE ET DE PYRAZOLE EN TANT QUE LIGANDS DE SOUS-TYPES DE RECEPTEURS DE LA DOPAMINE
    申请人:MERCK SHARP & DOHME LIMITED
    公开号:WO1995014672A1
    公开(公告)日:1995-06-01
    (EN) A class of substituted isoxazole and pyrazole derivatives of formula (I), or a salt thereof or a prodrug thereof, wherein the broken circle represents two non-adjacent double bonds whereby the five-membered ring containing X and Y is aromatic; one of X and Y represents nitrogen, and the other of X and Y represents oxygen or N-R5; R1 represents hydrogen, C1-6 alkyl or trifluoromethyl; R2 and R3 independently represent hydrogen, hydrocarbon, a heterocyclic group, halogen, cyano, trifluoromethyl, nitro, -ORa, -SRa, -SORa, -SO2Ra, -SO2NRaRb, -NRaRb, -NRaCORb, -NRaCO2Rb, -CORa, -CO2Ra or -CONRaRb; R4 represents hydrocarbon or a heterocyclic group; R5 represents hydrogen or C1-6 alkyl; and Ra and Rb independently represent hydrogen, hydrocarbon or a heterocyclic group, are ligands for dopamine receptor subtypes within the body and are therefore useful in the treatment and/or prevention of disorders of the dopamine system, in particular schizophrenia.(FR) L'invention se rapporte à une classe de dérivés d'isoxazole et de pyrazole substitués de la formule (I), ou à un sel de ces dérivés ou à un promédicament les contenant. Dans cette formule, le cercle en pointillé représente deux doubles liaisons non adjacentes grâce auxquelles le noyau à cinq éléments contenant X et Y est aromatique; un des éléments X et Y représente azote, et l'autre représente oxygène ou N-R5; R1 représente hydrogène, alkyle C1-6 ou trifluorométhyle; R2 et R3 représentent indépendamment hydrogène, hydrocarbure, un groupe hétérocyclique, halogène, cyano, trifluorométhyle, nitro, -ORa, -SRa, -SORa, -SO2Ra, -SO2NRaRb, -NRaRb, -NRaCORb, -NRaCO2Rb, -CORa, -CO2Ra ou -CONRaRb; R4 représente hydrocarbure ou un groupe hétérocyclique; R5 représente hydrogène ou alkyle C1-6; et Ra et Rb représentent indépendamment hydrogène, hydrocarbure ou un groupe hétérocyclique. Ces dérivés sont des ligands de sous-types de récepteurs de la dopamine agissant dans le corps humain et sont par conséquent utiles dans le traitement et/ou la prévention de troubles du système dopamine, notamment de la schizophrénie.
    本发明涉及一类亚恶唑和吡唑衍生物,其通式为(I),或这些衍生物的盐或前药。其中虚线圆环代表两个非相邻双键,使得含有X和Y的五元环是芳香族的;X和Y之一代表氮原子,另一者代表氧原子或N-R5;R1表示氢、C1-6烷基或三氟甲基;R2和R3各自独立地表示氢、烃类、杂环基团、卤素、氰基、三氟甲基、硝基、-ORa、-SRa、-SORa、-SO2Ra、-SO2NRaRb、-NRaRb、-NRaCORb、-NRaCO2Rb、-CORa、-CO2Ra或-CONRaRb;R4表示烃类或杂环基团;R5表示氢或C1-6烷基;Ra和Rb各自独立地表示氢、烃类或杂环基团。这些衍生物是体内多巴胺受体亚型的配体,因此可用于治疗和/或预防多巴胺系统相关的疾病,特别是精神分裂症。
  • ISOXAZOLE AND PYRAZOLE DERIVATIVES AS DOPAMINE RECEPTOR SUBTYPE LIGANDS
    申请人:MERCK SHARP & DOHME LTD.
    公开号:EP0730582A1
    公开(公告)日:1996-09-11
  • US5684006A
    申请人:——
    公开号:US5684006A
    公开(公告)日:1997-11-04
  • Substituted pyrazoles as novel selective ligands for the human dopamine D 4 receptor
    作者:Sylvie Bourrain、Ian Collins、Joseph G. Neduvelil、Michael Rowley、Paul D. Leeson、Smita Patel、Shil Patel、Frances Emms、Rosemarie Marwood、Kerry L. Chapman、Alan E. Fletcher、Graham A. Showell
    DOI:10.1016/s0968-0896(98)00134-5
    日期:1998.10
    Two novel series of 3-(heterocyclylmethyl)pyrazoles have been synthesised and evaluated as ligands for the human dopamine D-4 receptor. Compounds in series I (exemplified by 8k) have a phenyl ring joined to the 4-position of the pyrazole while those in series II (exemplified by 15j) have a 5-phenyl ring linked by a saturated chain to the 4-position of the pyrazole. Both series supplied compounds with excellent affinity for the human D-4 and good selectivity over other dopamine receptors. Excellent selectivity over calcium, sodium, and potassium ion channels was also achieved. (C) 1998 Elsevier Science Ltd. All rights reserved.
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