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(2'S,4R)-spiro[chromane-4,1'-cyclopropane]-2'-carboxylic acid

中文名称
——
中文别名
——
英文名称
(2'S,4R)-spiro[chromane-4,1'-cyclopropane]-2'-carboxylic acid
英文别名
Rac-(3'R,4S)-2,3-dihydrospiro[1-benzopyran-4,1'-cyclopropane]-3'-carboxylicacid;(1'S,4R)-spiro[2,3-dihydrochromene-4,2'-cyclopropane]-1'-carboxylic acid
(2'S,4R)-spiro[chromane-4,1'-cyclopropane]-2'-carboxylic acid化学式
CAS
——
化学式
C12H12O3
mdl
——
分子量
204.225
InChiKey
JXJOMJKPHPZPAD-BXKDBHETSA-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):
    1.7
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

反应信息

  • 作为反应物:
    描述:
    (2'S,4R)-spiro[chromane-4,1'-cyclopropane]-2'-carboxylic acidN-羟基-7-氮杂苯并三氮唑二氧化碳盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺三乙胺 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 20.0~30.0 ℃ 、10.0 MPa 条件下, 反应 16.0h, 生成 (1S,3aR,4S,7R,7aS)-N-((S)-1-amino-1-oxo-3-((S)-2-oxopyrrolidin-3-yl)propan-2-yl)-2-((2'R,4S)-spiro[chromane-4,1'-cyclopropane]-2'-carbonyl)-2,3,3a,4,7,7a-hexahydro-1H-4,7-methanoisoindole-1-carboxamide
    参考文献:
    名称:
    [EN] ANTI-VIRAL COMPOUNDS
    [FR] COMPOSÉS ANTI-VIRAUX
    摘要:
    Provided herein are compounds of Formula (I), or pharmaceutically acceptable salts thereof, pharmaceutical compositions that include a compound described herein (including pharmaceutically acceptable salts of a compound described herein) and methods of synthesizing the same. Also provided herein are methods of treating diseases and/or conditions with a compound of Formula (I), or a pharmaceutically acceptable salt thereof.
    公开号:
    WO2023283256A1
  • 作为产物:
    描述:
    ethyl rac-trans-spiro[chromane-4,1'-cyclopropane]-2'-carboxylate 在 、 lithium hydroxide 作用下, 以 甲醇乙二醇二甲醚 为溶剂, 以98 %的产率得到(2'S,4R)-spiro[chromane-4,1'-cyclopropane]-2'-carboxylic acid
    参考文献:
    名称:
    [EN] ANTI-VIRAL COMPOUNDS
    [FR] COMPOSÉS ANTI-VIRAUX
    摘要:
    Provided herein are compounds of Formula (I), or pharmaceutically acceptable salts thereof, pharmaceutical compositions that include a compound described herein (including pharmaceutically acceptable salts of a compound described herein) and methods of synthesizing the same. Also provided herein are methods of treating diseases and/or conditions with a compound of Formula (I), or a pharmaceutically acceptable salt thereof.
    公开号:
    WO2023283256A1
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文献信息

  • [EN] SPIROCYCLOPROPYLAMINE DERIVATIVES USEFUL AS INHIBITORS OF HISTONE DEMETHYLASES KDM1A<br/>[FR] DÉRIVÉS DE SPIROCYCLOPROPYLAMINE UTILES EN TANT QU'INHIBITEURS D'HISTONE DÉMÉTHYLASES KDM1A
    申请人:IEO - ST EUROPEO DI ONCOLOGIA S R L
    公开号:WO2017109061A1
    公开(公告)日:2017-06-29
    The present invention relates to provided spirocyclopropylamine compounds, endowed with a potent KDM1A (LSD1) inhibitory activity, wherein X, R, and R1 are as defined in the specification, pharmaceutical compositions containing such compounds and to their use in therapy.
    本发明涉及提供的螺环环丙胺化合物,具有强效的KDM1A(LSD1)抑制活性,其中X、R和R1如规范中所定义,包含这种化合物的药物组合物以及它们在治疗中的应用。
  • [EN] ANTI-VIRAL COMPOUNDS<br/>[FR] COMPOSÉS ANTI-VIRAUX
    申请人:[en]ALIGOS THERAPEUTICS, INC.
    公开号:WO2023283256A1
    公开(公告)日:2023-01-12
    Provided herein are compounds of Formula (I), or pharmaceutically acceptable salts thereof, pharmaceutical compositions that include a compound described herein (including pharmaceutically acceptable salts of a compound described herein) and methods of synthesizing the same. Also provided herein are methods of treating diseases and/or conditions with a compound of Formula (I), or a pharmaceutically acceptable salt thereof.
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