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tert-butyl 4-(chlorosulfonyl)-1H-indole-1-carboxylate | 2137573-51-2

中文名称
——
中文别名
——
英文名称
tert-butyl 4-(chlorosulfonyl)-1H-indole-1-carboxylate
英文别名
tert-butyl 4-chlorosulfonylindole-1-carboxylate
tert-butyl 4-(chlorosulfonyl)-1H-indole-1-carboxylate化学式
CAS
2137573-51-2
化学式
C13H14ClNO4S
mdl
——
分子量
315.777
InChiKey
DNYZTSLGQPQSBV-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):
    3.3
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    73.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    5-((1S,2R)-1-amino-2-(6-fluoro-2,3-dimethylphenyl)propyl)-1,3,4-oxadiazol-2(3H)-one monohydrochloride 、 tert-butyl 4-(chlorosulfonyl)-1H-indole-1-carboxylate吡啶 作用下, 反应 12.0h, 生成 N-((1S,2R)-2-(6-fluoro-2,3-dimethylphenyl)-1-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)propyl)-1H-indole-4-sulfonamide
    参考文献:
    名称:
    EP3466934
    摘要:
    公开号:
点击查看最新优质反应信息

文献信息

  • SULFONAMIDE COMPOUND OR SALT THEREOF
    申请人:Taiho Pharmaceutical Co., Ltd.
    公开号:EP3466934A1
    公开(公告)日:2019-04-10
    The present invention provides a novel sulfonamide compound having a ribonucleotide reductase inhibitory activity or a salt thereof, and a pharmaceutical composition containing the same as an active ingredient. A compound represented by Formula (I) [wherein, X1 represents an oxygen atom or the like; X2 represents an oxygen atom; X3 represents -NH-; X4 represents a hydrogen atom or the like; R1 represents -C(R11)(R12)- or the like; R11 and R12 are the same or different and each represents a hydrogen atom or the like; R2 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R3 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R4 represents a hydrogen atom or the like] or a salt thereof.
    本发明提供了一种具有核糖核苷酸还原酶抑制活性的新型磺酰胺化合物或其盐,以及含有该化合物作为活性成分的药物组合物。 由式(I)代表的化合物[其中,X1代表氧原子或类似物;X2代表氧原子;X3代表-NH-;X4代表氢原子或类似物;R1代表-C(R11)(R12)-或类似物;R11和R12相同或不同且各自代表氢原子或类似物;R2代表任选取代的C6-C14芳烃基团或类似物;R3代表任选取代的C6-C14芳烃基团或类似物;R4代表氢原子或类似物]或其盐。
  • ANTITUMOR AGENT
    申请人:Taiho Pharmaceutical Co., Ltd.
    公开号:EP3718545A1
    公开(公告)日:2020-10-07
    The present invention provides a method of enhancing an antitumor effect by a compound strongly inhibiting ribonucleotide reductase (RNR) or a salt thereof. A combination formulation involving combined administration of a sulfonamide compound represented by Formula (I) [In the formula, X1 represents an oxygen atom or the like; X2 represents an oxygen atom; X3 represents -NH-; X4 represents a hydrogen atom or the like; R1 represents -C(R11) (R12)- or the like; R11 and R12 are the same or different and each represents a hydrogen atom or the like; R2 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R3 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R4 represents a hydrogen atom or the like] or a salt thereof, having RNR inhibitory activity, and other antitumor agent(s).
    本发明提供了一种通过强抑制核糖核苷酸还原酶(RNR)的化合物或其盐增强抗肿瘤效果的方法。 一种组合制剂涉及联合给药由式(I)代表的磺酰胺化合物[式中,X1代表氧原子或类似物;X2代表氧原子;X3代表-NH-;X4代表氢原子或类似物;R1代表-C(R11)(R12)-或类似物;R11和R12相同或不同,各自代表氢原子或类似物;R2代表任选取代的C6-C14芳烃基团或类似物;R3代表任选取代的C6-C14芳烃基团或类似物;R4代表氢原子或类似物]或其盐,具有RNR抑制活性,以及其他抗肿瘤剂。
  • Sulfonamide compound or salt thereof
    申请人:Taiho Pharmaceutical Co., Ltd.
    公开号:US10889555B2
    公开(公告)日:2021-01-12
    The present invention provides a novel sulfonamide compound having a ribonucleotide reductase inhibitory activity or a salt thereof, and a pharmaceutical composition containing the same as an active ingredient. A compound represented by Formula (I) [wherein, X1 represents an oxygen atom or the like; X2 represents an oxygen atom; X3 represents —NH—; X4 represents a hydrogen atom or the like; R1 represents —C(R11)(R12)— or the like; R11 and R12 are the same or different and each represents a hydrogen atom or the like; R2 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R3 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R4 represents a hydrogen atom or the like] or a salt thereof.
    本发明提供了一种具有核糖核苷酸还原酶抑制活性的新型磺酰胺化合物或其盐,以及含有该化合物作为活性成分的药物组合物。 由式(I)代表的化合物[其中,X1代表氧原子或类似物;X2代表氧原子;X3代表-NH-;X4代表氢原子或类似物;R1代表-C(R11)(R12)-或类似物;R11和R12相同或不同且各自代表氢原子或类似物;R2代表任选取代的C6-C14芳烃基团或类似物;R3代表任选取代的C6-C14芳烃基团或类似物;R4代表氢原子或类似物]或其盐。
  • Sulfonamide Compound or Salt Thereof
    申请人:Taiho Pharmaceutical Co., Ltd.
    公开号:US20200157066A1
    公开(公告)日:2020-05-21
    The present invention provides a novel sulfonamide compound having a ribonucleotide reductase inhibitory activity or a salt thereof, and a pharmaceutical composition containing the same as an active ingredient. A compound represented by Formula (I) [wherein, X 1 represents an oxygen atom or the like; X 2 represents an oxygen atom; X 3 represents —NH—; X 4 represents a hydrogen atom or the like; R 1 represents —C(R 11 )(R 12 )— or the like; R 11 and R 12 are the same or different and each represents a hydrogen atom or the like; R 2 represents an optionally substituted C 6 -C 14 aromatic hydrocarbon group or the like; R 3 represents an optionally substituted C 6 -C 14 aromatic hydrocarbon group or the like; R 4 represents a hydrogen atom or the like] or a salt thereof.
  • Antitumor Agent
    申请人:Taiho Pharmaceutical Co., Ltd
    公开号:US20200405697A1
    公开(公告)日:2020-12-31
    The present invention provides a method of enhancing an antitumor effect by a compound strongly inhibiting ribonucleotide reductase (RNR) or a salt thereof. A combination formulation involving combined administration of a sulfonamide compound represented by Formula (I) [In the formula, X 1 represents an oxygen atom or the like; X 2 represents an oxygen atom; X 3 represents —NH—; X 4 represents a hydrogen atom or the like; R 1 represents —C(R 11 ) (R 12 )— or the like; R 11 and R 12 are the same or different and each represents a hydrogen atom or the like; R 2 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R 3 represents an optionally substituted C6-C14 aromatic hydrocarbon group or the like; R 4 represents a hydrogen atom or the like] or a salt thereof, having RNR inhibitory activity, and other antitumor agent(s).
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