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4-cyano-2-methylbenzenesulfonamide | 857003-69-1

中文名称
——
中文别名
——
英文名称
4-cyano-2-methylbenzenesulfonamide
英文别名
4-cyano-2-methyl-benzenesulfonic acid amide;4-Cyan-2-methyl-benzolsulfonsaeure-amid;4-Cyano-2-methylbenzene-1-sulfonamide
4-cyano-2-methylbenzenesulfonamide化学式
CAS
857003-69-1
化学式
C8H8N2O2S
mdl
MFCD16093758
分子量
196.23
InChiKey
ZPBWQJVJQZCWLG-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

物化性质

  • 熔点:
    195 °C
  • 沸点:
    418.9±55.0 °C(Predicted)
  • 密度:
    1.40±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    92.3
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2-chloro-6-[3-[[1-(trifluoromethyl)cyclopropyl]methoxy]pyrazol-1-yl]pyridine-3-carboxylic acid 、 4-cyano-2-methylbenzenesulfonamideN,N'-羰基二咪唑1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 四氢呋喃 为溶剂, 反应 16.5h, 以100%的产率得到2-chloro-N-(4-cyano-2-methyl-phenyl)sulfonyl-6-[3-[[1-(trifluoromethyl)cyclopropyl]methoxy]pyrazol-1-yl]pyridine-3-carboxamide
    参考文献:
    名称:
    [EN] MODULATOR OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR, PHARMACEUTICAL COMPOSITIONS, METHODS OF TREATMENT, AND PROCESS FOR MAKING THE MODULATOR
    [FR] MODULATEUR DE RÉGULATEUR DE CONDUCTANCE TRANSMEMBRANAIRE DE FIBROSE KYSTIQUE, COMPOSITIONS PHARMACEUTIQUES, PROCÉDÉS DE TRAITEMENT ET PROCÉDÉ DE FABRICATION DU MODULATEUR
    摘要:
    公开号:
    WO2018064632A8
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 sodium cyanide 、 nickel dichloride 作用下, 生成 4-cyano-2-methylbenzenesulfonamide
    参考文献:
    名称:
    Andrewes; King; Walker, Proceedings of the Royal Society of London, Series B: Biological Sciences, 1946, vol. 133, p. 20,35
    摘要:
    DOI:
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文献信息

  • [EN] ECTONUCLEOTIDE PYROPHOSPHATASE/PHOSPHODIESTERASE 1 (ENPP1) MODULATORS AND USES THEREOF<br/>[FR] MODULATEURS D'ECTONUCLÉOTIDES PYROPHOSPHATASES/PHOSPHODIESTÉRASES 1 (ENPP1) ET LEURS UTILISATIONS
    申请人:SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INST
    公开号:WO2021133915A1
    公开(公告)日:2021-07-01
    Provided herein are small molecule modulators of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), compositions comprising the compounds, and methods of using the compounds and compositions comprising the compounds.
    本文提供了外胞核苷酸焦磷酸酶/磷酸二酯酶1(ENPP1)的小分子调节剂,包括这些化合物的组合物,以及使用这些化合物和包含这些化合物的组合物的方法。
  • BIARYL AMIDE DERIVATIVE OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
    申请人:Katayama Seiji
    公开号:US20130116227A1
    公开(公告)日:2013-05-09
    Disclosed is a novel biaryl amide derivative represented by formula (1) and having an affinity for the aldosterone receptor; also disclosed is a pharmaceutically acceptable salt thereof. (In the formula, A is any of the groups represented by formula (a); L is —CONH—, etc.; R 1 is a substitutable aminosulfonyl group, etc.; R 2 is a hydrogen atom, etc.; R 3 is a hydrogen atom, etc.; R 4 is a hydrogen atom, a halogen atom, hydroxy group, a substitutable amino group, a substitutable C 1-6 alkoxy group, a substitutable 4- to 7-membered cyclic amino group, etc.; R 5a , R 5b and R 5c are each independently hydrogen atoms, etc.; R 6 is a halogen atom, a cyano group, etc.; R 7 and R 8 are each independently a hydrogen atom, etc.; and m is an integer such as 0.)
    揭示了一种表示为公式(1)的新型联苯酰胺衍生物,具有与醛固酮受体的亲和力;还揭示了其药用可接受的盐。(在该公式中,A是由公式(a)表示的任何基团之一;L是—CONH—等;R1是可替代的基磺酰基等;R2是氢原子等;R3是氢原子等;R4是氢原子、卤原子、羟基、可替代的基基团、可替代的C1-6烷氧基、可替代的4-到7-成员环基基团等;R5a、R5b和R5c各自独立地是氢原子等;R6是卤原子、基等;R7和R8各自独立地是氢原子等;m是整数,例如0。)
  • Modulator of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator
    申请人:Vertex Pharmaceuticals Incorporated
    公开号:US10570115B2
    公开(公告)日:2020-02-25
    Compounds of Formula I: pharmaceutically acceptable salts thereof, deuterated derivatives of any of the foregoing, and metabolites of any of the foregoing are disclosed. Pharmaceutical compositions comprising the same, methods of treating cystic fibrosis using the same, and methods for making the same are also disclosed.
    式 I 的化合物: 公开了其药学上可接受的盐、前述任一化合物的氚代衍生物以及前述任一化合物的代谢物。还公开了包含上述物质的药物组合物、使用上述物质治疗囊性纤维化的方法以及上述物质的制造方法。
  • MODULATOR OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR, PHARMACEUTICAL COMPOSITIONS, METHODS OF TREATMENT, AND PROCESS FOR MAKING THE MODULATOR
    申请人:Vertex Pharmaceuticals Incorporated
    公开号:EP3519401B1
    公开(公告)日:2021-09-29
  • Modulator of Cystic Fibrosis Transmembrane Conductance Regulator, Pharmaceutical Compositions, Methods of Treatment, and Process for Making the Modulator
    申请人:Vertex Pharmaceuticals Incorporated
    公开号:US20180093969A1
    公开(公告)日:2018-04-05
    Compounds of Formula I: pharmaceutically acceptable salts thereof, deuterated derivatives of any of the foregoing, and metabolites of any of the foregoing are disclosed. Pharmaceutical compositions comprising the same, methods of treating cystic fibrosis using the same, and methods for making the same are also disclosed.
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