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()-5-{2-hydroxy-3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-trifluoromethyl-propionylamino}-phthalide | 600730-96-9

中文名称
——
中文别名
——
英文名称
()-5-{2-hydroxy-3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-trifluoromethyl-propionylamino}-phthalide
英文别名
3,3,3-trifluoro-2-[[1-[2-fluoro-5-(trifluoromethyl)phenyl]cyclopropyl]methyl]-2-hydroxy-N-(1-oxo-3H-2-benzofuran-5-yl)propanamide
()-5-{2-hydroxy-3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-trifluoromethyl-propionylamino}-phthalide化学式
CAS
600730-96-9;600730-97-0;600730-98-1
化学式
C22H16F7NO4
mdl
——
分子量
491.362
InChiKey
UAXPVEKEMXWFNV-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):
    4.8
  • 重原子数:
    34
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    75.6
  • 氢给体数:
    2
  • 氢受体数:
    11

上下游信息

反应信息

  • 作为产物:
    描述:
    5-{3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-oxo-propionylamino}-phthalide 、 (三氟甲基)三甲基硅烷四丁基氟化铵 caesium carbonate 作用下, 以 DMF (N,N-dimethyl-formamide) 、 四氢呋喃 为溶剂, 反应 19.0h, 生成 ()-5-{2-hydroxy-3-[1-(2-fluoro-5-trifluoromethylphenyl)-cyclopropyl]-2-trifluoromethyl-propionylamino}-phthalide
    参考文献:
    名称:
    Non-steroidal progesting
    摘要:
    本发明涉及一般式(I)的非甾体孕酮类似物,其中R1和R2分别为—H或—F,R3为—CH3或—CF3,Ar为2或其药物可接受的衍生物或类似物。这些孕酮类似物适用于在不同的靶组织中选择性调节孕激素受体介导的效应,特别是在子宫组织与乳腺组织中。因此,本发明的孕酮类似物,可选配雌激素,可用于避孕(特别是在无雌激素口服避孕药中)、激素替代疗法和治疗妇科疾病。本发明还涉及在不同的靶组织或器官中选择性调节孕激素受体介导的效应的方法。
    公开号:
    US20030232824A1
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文献信息

  • 5- 2-hydroxy-3-[1-(3-trifluoromethylphenyl)-cyclopropyl]-propionylamino -phtalide and 6- 2-hydroxy-3-[1-(3-trifluoromethylphenyl)-cyclopropyl]-propionylamino -4-methyl-2,3-benzoxazin-1-one derivatives with progesterone receptor modulating activity for use in fertility control, hormone replacement therapy and the treatment of gynecological disorders
    申请人:Schering Aktiengesellschaft
    公开号:EP1344776A1
    公开(公告)日:2003-09-17
    The present invention relates to non-steroidal progestins of the general formula (I) wherein R1 and R2 are independently of each other -H or -F, R3 is -CH3 or -CF3, and Ar is or a pharmaceutically acceptable derivative or analogue thereof. These progestins are suitable for selectively modulating progesterone receptor mediated effects in different target tissues, particularly in uterine tissue versus breast tissue. Therefore, the progestins of the present invention, optionally in combination with estrogens, may be used for contraception, hormone replacement therapy and the treatment of gynecological disorders. The present invention furthermore relates to methods for selectively modulating progesterone receptor mediated effects in different target tissues or organs.
    本发明涉及通式(I)的非类固醇孕激素,其中R1和R2独立地为-H或-F,R3为-CH3或-CF3,而Ar为或其药物可接受的衍生物或类似物。这些孕激素适用于在不同的靶组织中选择性调节孕激素受体介导的效应,特别是在子宫组织与乳腺组织中。因此,本发明的孕激素,可选择性与雌激素联合使用,可用于避孕、激素替代疗法以及妇科疾病的治疗。本发明还涉及在不同的靶组织或器官中选择性调节孕激素受体介导的效应的方法。
  • Pharmaceutical preparation for continuous hormonal treatment over a period of longer than 21-28 days comprising two estrogen and/or progestin compositions
    申请人:Schering Aktiengesellschaft
    公开号:EP1535618A1
    公开(公告)日:2005-06-01
    A pharmaceutical preparation to obtain a continuous hormonal treatment over a desired period of time longer than 21-28 days comprising a first composition containing at least one estrogen and/or at least one progestin in a predetermined amount to be administered in the first 21-28 days and a second composition which contains at least one estrogen and/or at least one progestin in a predetermined amount higher than the amount of the first composition and comprises a mono or multiphase sequence of pharmaceutical dosages.
    一种可在超过 21-28 天的预期时间内获得持续荷尔蒙治疗的药物制剂,包括一种第一组合物,其中含有至少一种雌激素和/或至少一种孕激素,其预定用量在前 21-28 天内给药,以及一种第二组合物,其中含有至少一种雌激素和/或至少一种孕激素,其预定用量高于第一组合物的用量,并包括单相或多相的药物剂量序列。
  • Pharmaceutical preparation for continuous hormonal treatment over a period of 21-28 days comprising two ethinylestradio or estradio and drospirenone compositions
    申请人:Bayer Schering Pharma Aktiengesellschaft
    公开号:EP2044942A1
    公开(公告)日:2009-04-08
    A pharmaceutical preparation to obtain a continuous hormonal treatment over a desired period of time longer than 21-28 days comprising a first composition containing at least one estrogen and/or at least one progestin in a predetermined amount to be administered in the first 21-28 days and a second composition which contains at least one estrogen and/or at least one progestin in a predetermined amount higher than the amount of the first composition and comprises a mono or multiphase sequence of pharmaceutical dosages.
    一种可在超过 21-28 天的预期时间内获得持续荷尔蒙治疗的药物制剂,包括一种第一组合物,其中含有至少一种雌激素和/或至少一种孕激素,其预定用量在前 21-28 天内给药,以及一种第二组合物,其中含有至少一种雌激素和/或至少一种孕激素,其预定用量高于第一组合物的用量,并包括单相或多相的药物剂量序列。
  • 5-(2-HYDROXY-3-'1-(3-TRIFLUOROMETHYLPHENYL)-CYCLOPROPL!-PROPIONYLAMINO)-PHTALIDE AND RELATED COMPOUNDS WITH PROGESTERONE RECEPTOR MODULATING ACTIVITY FOR USE IN FERTILITY CONTROL AND HORMONE REPLACEMENT THERAPY
    申请人:Schering AG
    公开号:EP1482925A1
    公开(公告)日:2004-12-08
  • 5-(2-HYDROXY-3-'1-(3-TRIFLUOROMETHYLPHENYL)-CYCLOPROPL]-PROPIONYLAMINO)-PHTALIDE AND RELATED COMPOUNDS WITH PROGESTERONE RECEPTOR MODULATING ACTIVITY FOR USE IN FERTILITY CONTROL AND HORMONE REPLACEMENT THERAPY
    申请人:Schering AG
    公开号:EP1482925B1
    公开(公告)日:2007-01-17
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