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3-[2(R)-tert-butoxycarbonylamino-2-phenylethyl]-5-(3-hydroxyphenyl)-1-[2-bromo-6-fluorobenzyl]-6-methylpyrimidine-2,4(1H,3H)-dione | 832711-04-3

中文名称
——
中文别名
——
英文名称
3-[2(R)-tert-butoxycarbonylamino-2-phenylethyl]-5-(3-hydroxyphenyl)-1-[2-bromo-6-fluorobenzyl]-6-methylpyrimidine-2,4(1H,3H)-dione
英文别名
tert-butyl N-[(1R)-2-[3-[(2-chloro-6-fluorophenyl)methyl]-5-(3-hydroxyphenyl)-4-methyl-2,6-dioxopyrimidin-1-yl]-1-phenylethyl]carbamate
3-[2(R)-tert-butoxycarbonylamino-2-phenylethyl]-5-(3-hydroxyphenyl)-1-[2-bromo-6-fluorobenzyl]-6-methylpyrimidine-2,4(1H,3H)-dione化学式
CAS
832711-04-3
化学式
C31H31ClFN3O5
mdl
——
分子量
580.056
InChiKey
HTKSFDJKBQZTQI-SANMLTNESA-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):
    5.5
  • 重原子数:
    41
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    99.2
  • 氢给体数:
    2
  • 氢受体数:
    6

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

  • 作为产物:
    描述:
    3-[2(R)-tert-butoxycarbonylamino-2-phenylethyl]-5-bromo-1-[2-bromo-6-fluorobenzyl]-6-methylpyrimidine-2,4(1H,3H)-dione3-羟基苯硼酸四(三苯基膦)钯 barium dihydroxidepotassium carbonate 作用下, 以 乙醇甲苯 为溶剂, 反应 16.0h, 以98%的产率得到3-[2(R)-tert-butoxycarbonylamino-2-phenylethyl]-5-(3-hydroxyphenyl)-1-[2-bromo-6-fluorobenzyl]-6-methylpyrimidine-2,4(1H,3H)-dione
    参考文献:
    名称:
    [EN] PYRIMIDINE-2,4-DIONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS
    [FR] DERIVES DE PYRIMIDINE-2,4-DIONE, SERVANT D'ANTAGONISTES AU RECEPTEUR DE L'HORMONE DE LIBERATION DE LA GONADOTROPINE
    摘要:
    GnRH受体拮抗剂已被披露,可用于治疗男性和女性的各种与性激素相关的疾病。本发明的化合物具有结构式(I),其中R1a、R1b、R2a、R2b、R3、R4、R5、R6、R7和X如本文所定义,包括立体异构体、前药和其药用盐。此外,还披露了含有本发明化合物的组合物,该组合物与药用载体结合,以及涉及使用该组合物来拮抗需要此类治疗的受试者的促性腺激素释放激素的方法。
    公开号:
    WO2005007164A1
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文献信息

  • Gonadotropin-releasing hormone receptor antagonists and methods relating thereto
    申请人:Zhu Yun-Fei
    公开号:US20050043338A1
    公开(公告)日:2005-02-24
    GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R 1a , R 1b , R 2a , R 2b , R 3 , R 4 , R 5 , R 6 , R 7 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
    本发明披露了GnRH受体拮抗剂,可用于治疗男性和女性的各种性激素相关疾病。本发明的化合物具有以下结构:其中R1a、R1b、R2a、R2b、R3、R4、R5、R6、R7和X的定义如本文所述,包括立体异构体、前药和其药学上可接受的盐。还披露了含有本发明化合物的组合物与药学上可接受的载体,以及与其相关的方法,用于对需要拮抗促性腺激素释放激素的受体的患者进行治疗。
  • PYRIMIDINE-2,4-DIONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS
    申请人:NEUROCRINE BIOSCIENCES, INC.
    公开号:EP1660091A1
    公开(公告)日:2006-05-31
  • US7071200B2
    申请人:——
    公开号:US7071200B2
    公开(公告)日:2006-07-04
  • US7329669B2
    申请人:——
    公开号:US7329669B2
    公开(公告)日:2008-02-12
  • [EN] PYRIMIDINE-2,4-DIONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS<br/>[FR] DERIVES DE PYRIMIDINE-2,4-DIONE, SERVANT D'ANTAGONISTES AU RECEPTEUR DE L'HORMONE DE LIBERATION DE LA GONADOTROPINE
    申请人:NEUROCRINE BIOSCIENCES INC
    公开号:WO2005007164A1
    公开(公告)日:2005-01-27
    GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure formula (I) wherein R1a, R1b, R2a, R2b, R3, R4, R5, R6, R7 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
    GnRH受体拮抗剂已被披露,可用于治疗男性和女性的各种与性激素相关的疾病。本发明的化合物具有结构式(I),其中R1a、R1b、R2a、R2b、R3、R4、R5、R6、R7和X如本文所定义,包括立体异构体、前药和其药用盐。此外,还披露了含有本发明化合物的组合物,该组合物与药用载体结合,以及涉及使用该组合物来拮抗需要此类治疗的受试者的促性腺激素释放激素的方法。
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