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(1R,2R)-4,6-dichloro-1-(dimethylamino)-2,3-dihydro-1H-inden-2-ol | 1571104-01-2

中文名称
——
中文别名
——
英文名称
(1R,2R)-4,6-dichloro-1-(dimethylamino)-2,3-dihydro-1H-inden-2-ol
英文别名
——
(1R,2R)-4,6-dichloro-1-(dimethylamino)-2,3-dihydro-1H-inden-2-ol化学式
CAS
1571104-01-2
化学式
C11H13Cl2NO
mdl
——
分子量
246.136
InChiKey
RMMFWDGFXLKKJL-GHMZBOCLSA-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):
    2.5
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    23.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    (1R,2R)-4,6-dichloro-1-(dimethylamino)-2,3-dihydro-1H-inden-2-oltert-butyl 2-(2-(2-(4-hydroxyphenylsulfonamido)ethoxy)ethoxy)ethylcarbamate偶氮二甲酸二异丙酯三苯基膦 作用下, 以 四氢呋喃 为溶剂, 反应 16.0h, 以510 mg的产率得到2-(2-(2-(4-((1S,2S)-4,6-dichloro-2-(dimethylamino)-2,3-dihydro-1H-inden-1-yloxy)phenylsulfonamido)ethoxy)ethoxy)ethylcarbamic acid tert-butyl ester
    参考文献:
    名称:
    [EN] COMPOUNDS AND METHODS FOR INHIBITING NHE-MEDIATED ANTIPORT IN THE TREATMENT OF DISORDERS ASSOCIATED WITH FLUID RETENTION OR SALT OVERLOAD AND GASTROINTESTINAL TRACT DISORDERS
    [FR] COMPOSÉS ET PROCÉDÉS D'INHIBITION D'UN ANTIPORT À MÉDIATION PAR NHE DANS LE TRAITEMENT DE TROUBLES ASSOCIÉS À UNE RÉTENTION DE FLUIDE OU À UNE SURCHARGE DE SEL ET DE TROUBLES DU TRACTUS GASTRO-INTESTINAL
    摘要:
    本公开涉及化合物和治疗液体潴留或盐过多相关疾病的方法,例如心力衰竭(特别是充血性心力衰竭)、慢性肾脏疾病、晚期肾脏疾病、肝脏疾病和过氧化物酶体增殖物激活受体(PPAR)γ激动剂诱导的液体潴留。本公开还涉及化合物和治疗高血压的方法。本公开还涉及化合物和治疗胃肠道疾病的方法,包括治疗或减轻与胃肠道疾病相关的疼痛。
    公开号:
    WO2014029983A1
点击查看最新优质反应信息

文献信息

  • COMPOUNDS AND METHODS FOR INHIBITING NHE-MEDIATED ANTIPORT IN THE TREATMENT OF DISORDERS ASSOCIATED WITH FLUID RETENTION OR SALT OVERLOAD AND GASTROINTESTINAL TRACT DISORDERS
    申请人:ARDELYX, INC.
    公开号:US20150336892A1
    公开(公告)日:2015-11-26
    The present disclosure is directed to compounds and methods for the treatment of disorders associated with fluid retention or salt overload, such as heart failure (in particular, congestive heart failure), chronic kidney disease, end-stage renal disease, liver disease, and peroxisome proliferator-activated receptor (PPAR) gamma agonist-induced fluid retention. The present disclosure is also directed to compounds and methods for the treatment of hypertension. The present disclosure is also directed to compounds and methods for the treatment of gastrointestinal tract disorders, including the treatment or reduction of pain associated with gastrointestinal tract disorders.
    本公开涉及化合物和方法,用于治疗与液体潴留或盐过量相关的疾病,例如心力衰竭(特别是充血性心力衰竭)、慢性肾脏疾病、晚期肾脏疾病、肝病和过氧化物酶体增殖物激活受体(PPAR)γ激动剂引起的液体潴留。本公开还涉及化合物和方法,用于治疗高血压。本公开还涉及化合物和方法,用于治疗胃肠道疾病,包括治疗或减轻与胃肠道疾病相关的疼痛。
  • Compounds and methods for inhibiting NHE-mediated antiport in the treatment of disorders associated with fluid retention or salt overload and gastrointestinal tract disorders
    申请人:ARDELYX, INC
    公开号:US10376481B2
    公开(公告)日:2019-08-13
    The present disclosure is directed to compounds and methods for the treatment of disorders associated with fluid retention or salt overload, such as heart failure (in particular, congestive heart failure), chronic kidney disease, end-stage renal disease, liver disease, and peroxisome proliferator-activated receptor (PPAR) gamma agonist-induced fluid retention. The present disclosure is also directed to compounds and methods for the treatment of hypertension. The present disclosure is also directed to compounds and methods for the treatment of gastrointestinal tract disorders, including the treatment or reduction of pain associated with gastrointestinal tract disorders.
    本公开内容涉及用于治疗与体液潴留或盐负荷过重相关的疾病的化合物和方法,如心力衰竭(尤其是充血性心力衰竭)、慢性肾病、终末期肾病、肝病和过氧化物酶体增殖激活受体(PPAR)γ激动剂诱导的体液潴留。本公开还涉及治疗高血压的化合物和方法。本公开还涉及治疗胃肠道疾病的化合物和方法,包括治疗或减轻与胃肠道疾病相关的疼痛。
  • Compounds useful for treating gastrointestinal tract disorders
    申请人:Ardelyx, Inc.
    公开号:US11242337B2
    公开(公告)日:2022-02-08
    The present disclosure is directed to compounds and methods for the treatment of disorders associated with fluid retention or salt overload, such as heart failure (in particular, congestive heart failure), chronic kidney disease, end-stage renal disease, liver disease, and peroxisome proliferator-activated receptor (PPAR) gamma agonist-induced fluid retention. The present disclosure is also directed to compounds and methods for the treatment of hypertension. The present disclosure is also directed to compounds and methods for the treatment of gastrointestinal tract disorders, including the treatment or reduction of pain associated with gastrointestinal tract disorders.
    本公开内容涉及用于治疗与体液潴留或盐负荷过重相关的疾病的化合物和方法,如心力衰竭(尤其是充血性心力衰竭)、慢性肾病、终末期肾病、肝病和过氧化物酶体增殖激活受体(PPAR)γ激动剂诱导的体液潴留。本公开还涉及治疗高血压的化合物和方法。本公开还涉及治疗胃肠道疾病的化合物和方法,包括治疗或减轻与胃肠道疾病相关的疼痛。
  • [EN] COMPOUNDS AND METHODS FOR INHIBITING NHE-MEDIATED ANTIPORT IN THE TREATMENT OF DISORDERS ASSOCIATED WITH FLUID RETENTION OR SALT OVERLOAD AND GASTROINTESTINAL TRACT DISORDERS<br/>[FR] COMPOSÉS ET PROCÉDÉS D'INHIBITION D'UN ANTIPORT À MÉDIATION PAR NHE DANS LE TRAITEMENT DE TROUBLES ASSOCIÉS À UNE RÉTENTION DE FLUIDE OU À UNE SURCHARGE DE SEL ET DE TROUBLES DU TRACTUS GASTRO-INTESTINAL
    申请人:ARDELYX INC
    公开号:WO2014029983A1
    公开(公告)日:2014-02-27
    The present disclosure is directed to compounds and methods for the treatment of disorders associated with fluid retention or salt overload, such as heart failure (in particular, congestive heart failure), chronic kidney disease, end-stage renal disease, liver disease, and peroxisome proliferator-activated receptor (PPAR) gamma agonist-induced fluid retention. The present disclosure is also directed to compounds and methods for the treatment of hypertension. The present disclosure is also directed to compounds and methods for the treatment of gastrointestinal tract disorders, including the treatment or reduction of pain associated with gastrointestinal tract disorders.
    本公开涉及化合物和治疗液体潴留或盐过多相关疾病的方法,例如心力衰竭(特别是充血性心力衰竭)、慢性肾脏疾病、晚期肾脏疾病、肝脏疾病和过氧化物酶体增殖物激活受体(PPAR)γ激动剂诱导的液体潴留。本公开还涉及化合物和治疗高血压的方法。本公开还涉及化合物和治疗胃肠道疾病的方法,包括治疗或减轻与胃肠道疾病相关的疼痛。
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