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Ethyl 3-(4-methoxyphenyl)sulfanylpropanoate | 28744-00-5

中文名称
——
中文别名
——
英文名称
Ethyl 3-(4-methoxyphenyl)sulfanylpropanoate
英文别名
——
Ethyl 3-(4-methoxyphenyl)sulfanylpropanoate化学式
CAS
28744-00-5
化学式
C12H16O3S
mdl
MFCD01934461
分子量
240.323
InChiKey
HXNJQIZBDYDTFM-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):
    2.6
  • 重原子数:
    16
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.416
  • 拓扑面积:
    60.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    Ethyl 3-(4-methoxyphenyl)sulfanylpropanoate六氟异丙醇 、 lithium perchlorate 、 溶剂黄146 作用下, 反应 8.0h, 以58%的产率得到3-[(4-methoxyphenyl)sulfonyl]propanoic acid ethyl ester
    参考文献:
    名称:
    硫醚的电化学氧化:使用氢键网络调节氧化电位
    摘要:
    开发了一种高效的硫醚化学选择性电化学氧化为亚砜和砜的方法。由六氟-2-丙醇(HFIP)和乙酸(AcOH)生成的氢键网络在氧化电位的调节中起重要作用。氢键网络与亚砜牢固地络合,使其不易进一步氧化。因此,硫醚可以被选择性地电化学氧化成亚砜,并且过氧化可以被最小化。此外,密度泛函理论(DFT)计算和循环伏安法实验支持了这种通过氢键进行的氧化调节。
    DOI:
    10.1016/j.elecom.2019.106583
  • 作为产物:
    描述:
    4,4'-二甲氧基二苯二硫丙烯酸乙酯二氯二茂钛 作用下, 以 四氢呋喃 为溶剂, 反应 4.5h, 以87%的产率得到Ethyl 3-(4-methoxyphenyl)sulfanylpropanoate
    参考文献:
    名称:
    Zn/Cp 2 TiCl 2还原 S-S 键断裂:在β-芳硫羰基化合物合成中的应用
    摘要:
    二芳基二硫化物在室温下在干燥的 THF 中被 Zn/Cp2TiCl2 系统有效还原,得到相应的亲核硫阴离子-二茂钛络合物,然后与 α, β-不饱和酯(酮或腈)反应得到相应的 β-芳硫酯(酮或腈)收率良好。
    DOI:
    10.3184/030823409x12592534682310
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文献信息

  • Liquid/liquid separation of polysiloxane-supported catalysts
    作者:Melissa A. Grunlan、Katherine R. Regan、David E. Bergbreiter
    DOI:10.1039/b601120a
    日期:——
    Liquid/liquid separation after monophasic reactions is a viable way to use and recover polysiloxane-supported catalysts.
    单相反应后的液/液分离是使用和回收聚硅氧烷负载型催化剂的可行方法。
  • [EN] N-HYDROXY-2-(ALKYL, ARYL, OR HETEROARYL SULFANYL, SULFINYL OR SULFONYL)-3-SUBSTITUTED-ALKYL, ARYL OR HETEROARYLAMIDES AS MATRIX METALLOPROTEINASE INHIBITORS<br/>[FR] ALKYLE, ARYLE OU HETEROARYLAMIDES N-HYDROXY-2-(ALKYL, ARYL OU HETEROARYL SULFANYL, SULFINYL OU SULFONYL)-3-SUBSTITUES EN TANT QU'INHIBITEURS DE LA METALLOPROTEINASE MATRICIELLE
    申请人:AMERICAN CYANAMID COMPANY
    公开号:WO1999042436A1
    公开(公告)日:1999-08-26
    (EN) Matrix metalloproteinases (MMPs) are a group of enzymes that have been implicated in the pathological destruction of connective tissue and basement membranes. These zinc containing endopeptidases consist of several subsets of enzymes including collagenases, stromelysins and gelatinases. TNF-$g(a) converting enzyme (TACE), a pro-inflammatory cytokine, catalyzes the formation of TNF-$g(a) from membrane bound TNF-$g(a) precursor protein. It is expected that small molecule inhibitors of MMPs and TACE therefore have the potential for treating a variety of disease states. The present invention provides low molecular weight, non-peptide inhibitors of matrix metalloproteinases (MMPs) and TNF-$g(a) converting enzyme (TACE) for the treatment of arthritis, tumor metastasis, tissue ulceration, abnormal wound healing, periodontal disease, bone disease, diabetes (insulin resistance) and HIV infection having formula (I), wherein R2 and R3 form a heterocyclic ring and A is S, S(O), or S(O)2 and R1 and R4 are defined herein.(FR) L'invention concerne les métalloprotéinases matricielles (MMP) qui sont un groupe d'enzymes impliquées dans la destruction pathologique d'un tissu conjonctif et d'une membrane basale. Ces endopeptidases contenant du zinc sont formée de différents sous-ensembles d'enzymes comprenant des collagénases, des stomélysines et des gélatinases. L'enzyme de conversion TNF-$g(a) (TACE), une cytokine pro-inflammatoire, catalyse la formation de TNF-$g(a) à partir d'une membrane liée à la protéine précurseur TNF-$g(a). On pense que de petits inhibiteurs de molécules de MMP et TACE sont en mesure de traiter un certain nombre de pathologies. L'invention concerne en outre des inhibiteurs non peptidiques à faible poids moléculaire de métalloprotéinases matricielles (MMP) et d'une enzyme de conversion TNF-$g(a) (TACE) pour le traitement de l'arthrite, de métastases tumorales, d'ulcération tissulaire, de subérification d'une blessure anormale, de parodontopathie, de maladies osseuses, du diabète (résistance insulinique) de l'infection par VIH de formule (I), dans laquelle R2 et R3 désignent un noyau hétérocyclique et A désigne S, S(O) ou S(O)2 et R1 et R4 sont tels que définis.
    基质金属蛋白酶(MMPs)是一组酶,已被认为参与了结缔组织和基底膜的病理性破坏。这些含锌的内切酶包括几个亚组酶,包括胶原酶、基质金属蛋白酶和明胶酶。TNF-$g(a)转化酶(TACE)是一种促炎细胞因子,催化膜结合型TNF-$g(a)前体蛋白形成TNF-$g(a)。因此,MMPs和TACE的小分子抑制剂具有治疗多种疾病的潜力。本发明提供了低分子量、非肽类基质金属蛋白酶(MMPs)和TNF-$g(a)转化酶(TACE)的抑制剂,用于治疗关节炎、肿瘤转移、组织溃疡、异常伤口愈合、牙周病、骨病、糖尿病(胰岛素抵抗)和HIV感染,其化学式为(I),其中R2和R3形成杂环环,A为S、S(O)或S(O)2,R1和R4如本文所定义。
  • [EN] N-HYDROXY-2-(ALKYL, ARYL, OR HETEROARYL SULFANYL, SULFINYL OR SULFONYL)-3-SUBSTITUTED ALKYL, ARYL OR HETEROARYLAMIDES AS MATRIX METALLOPROTEINASE INHIBITORS<br/>[FR] N-HYDROXY-2-(ALKYL,ARYL OU HETEROARYL SULFANYL, SULFINYL OU SULFONYL)-ALKYL, ARYL OU HETEROARYLAMIDES SUBSTITUES EN POSITION 3, UTILISES COMME INHIBITEURS DES METALLOPROTEINASE MATRICIELLE
    申请人:AMERICAN CYANAMID COMPANY
    公开号:WO1998038163A1
    公开(公告)日:1998-09-03
    (EN) Matrix metalloproteinases (MMPs) are a group of enzymes that have been implicated in the pathological destruction of connective tissue and basement membranes. These zinc containing endopeptidases consist of several subsets of enzymes including collagenases, stromelysins and gelatinases. TNF-$g(a) converting enzymes (TACE), a pro-inflammatory cytokine, catalyze the formation of TNF-$g(a) from membrane-bound TNF-$g(a) precursor protein. It is expected that small molecule inhibitors of MMPs and TACE therefore have the potential for treating a variety of disease states. The present invention provides low molecular weight, non-peptide inhibitors of matrix metalloproteinases (MMPs) and TNF-$g(a) converting enzyme (TACE) for the treatment of arthritis, tumor metastasis, tissue ulceration, abnormal wound healing, periodontal disease, bone disease, diabetes (insulin resistance) and HIV infection. The compounds of this invention are represented by formula (I), where R1, R2, R3 and R4 are described herein.(FR) Les métalloprotéinases matricielles (MMP) sont un groupe d'enzymes ayant été impliquées dans la destruction pathologique de la membrane basale et du tissu conjonctif. Ces endopeptidases contenant du zinc consistent en plusieurs sous-ensembles d'enzymes comprenant des collagénases, des stromélysines et des gélatinases. L'enzyme de conversion de TNF-$g(a) (TACE), une cytokine pro-inflammatoire, catalyse la formation de TNF-$g(a) à partir de la protéine précurseur de TNF-$g(a) liée à la membrane. On suppose que les inhibiteurs à petites molécules de MMP et TACE ont donc la capacité de traiter plusieurs états pathologiques. L'invention se rapporte à des inhibiteurs de non peptides, à faible poids moléculaire, des métalloprotéinases matricielles (MMP) et à l'enzyme de conversion TNF-$g(a) (TACE) pour le traitement de l'arthrite, de métastases tumorales, de l'ulcération de tissu, de cicatrisation anormale, de la parodontopathie, les maladies osseuses, de diabètes (résistance à l'insuline) et de l'infection au VIH. Les composés de l'invention sont représentés par la formule (I), R1, R2, R3 et R4 étant décrits.
    基质金属蛋白酶(MMP)是一组酶,已被认为参与了结缔组织和基底膜的病理性破坏。这些含锌的内切酶由几个亚组成,包括胶原酶、基质金属蛋白酶和明胶酶。TNF-$g(a)转化酶(TACE)是一种促炎细胞因子,可催化膜结合型TNF-$g(a)前体蛋白形成TNF-$g(a)。因此,MMP和TACE的小分子抑制剂有望治疗多种疾病。本发明提供了用于治疗关节炎、肿瘤转移、组织溃疡、异常伤口愈合、牙周病、骨病、糖尿病(胰岛素抵抗)和HIV感染的基质金属蛋白酶(MMP)和TNF-$g(a)转化酶(TACE)的低分子量非肽抑制剂。本发明的化合物由公式(I)表示,其中R1、R2、R3和R4如本文所述。
  • N-hydroxy-2-(alkyl, aryl, or heteroaryl sulfanyl, sulfinyl, or sulfonyl)-3-substituted alkyl, aryl or heteroarylamides as matrix metalloproteinase inhibitors
    申请人:American Cyanamid Company
    公开号:US20020188120A1
    公开(公告)日:2002-12-12
    Matrix metalloproteinases (MMPs) are a group of enzymes that have been implicated in the pathological destruction of connective tissue and basement membranes. These zinc containing endopeptidases consist of several subsets of enzymes including collagenases, stromelysins and gelatinases. TNF-&agr; converting enzyme (TACE), a pro-inflammatory cytokine, catalyzes the formation of TNF-&agr; from membrane bound TNF-&agr; precursor protein. It is expected that small molecule inhibitors of MMPs and TACE therefore have the potential for treating a variety of disease states. The present invention provides low molecular weight, non-peptide inhibitors of matrix metalloproteinases (MMPs) and TNF-&agr; converting enzyme (TACE) for the treatment of arthritis, tumor metastasis, tissue ulceration, abnormal wound healing, periodontal disease, bone disease, diabetes (insulin resistance) and HIV infection having the formula 1 wherein R 2 and R 3 form a heterocyclic ring and A is S, S(O), or S(O)2, and R 1 and R 4 are defined herein.
    基质金属蛋白酶(MMPs)是一组酶,已被认为与结缔组织和基底膜的病理性破坏有关。这些含锌内切酶包括几个酶亚组,包括胶原酶、基质金属蛋白酶和明胶酶。TNF-α转化酶(TACE)是一种促炎细胞因子,催化膜结合的TNF-α前体蛋白形成TNF-α。因此,MMPs和TACE的小分子抑制剂有潜力用于治疗多种疾病状态。本发明提供了基质金属蛋白酶(MMPs)和TNF-α转化酶(TACE)的低分子量、非肽抑制剂,用于治疗关节炎、肿瘤转移、组织溃疡、异常伤口愈合、牙周病、骨病、糖尿病(胰岛素抵抗)和HIV感染,其化学式为1,其中R2和R3形成杂环环,A为S、S(O)或S(O)2,R1和R4如本文所定义。
  • N-hydroxy-2-(alkyl, aryl, or heteroaryl sulfanyl, sulfinyl or sulfonyl)-3-substituted alkyl, aryl or heteroarylamides as matrix metalloproteinase inhibitors
    申请人:American Cyanamid Company
    公开号:US20020032186A1
    公开(公告)日:2002-03-14
    Matrix metalloproteinases (MMPs) are a group of enzymes that have been implicated in the pathological destruction of connective tissue and basement membranes. These zinc containing endopeptidases consist of several subsets of enzymes including collagenases, stromelysins and gelatinases. TNF-&agr; converting enzyme (TACE), a pro-inflmatory cytokine, catalyzes the formation of TNF-&agr; from membrane bound TNF-&agr; precursor protein. It is expected that small molecule inhibitors of MMPs and TACE therefore have the potential for treating a variety of disease states. The present invention provides low molecular weight, non-peptide inhibitors of matrix metalloproteinases (MMPs) and TNF-&agr; converting enzyme (TACE) for the treatment of arthritis, tumor metastasis, tissue ulceration, abnormal wound healing, periodontal disease, bone disease, diabetes (insulin resistance) and HIV infection having the formula 1 wherein R 2 and R 3 form a heterocyclic ring and A is S, S(O), or S(O) 2 , and R 1 and R 4 are defined herein.
    基质金属蛋白酶(MMPs)是一组酶,已被证明与结缔组织和基底膜的病理性破坏有关。这些含锌内切酶包括几个亚组酶,包括胶原酶、基质金属蛋白酶和明胶酶。TNF-α转化酶(TACE)是一种促炎细胞因子,它催化从膜结合的TNF-α前体蛋白形成TNF-α。因此,MMPs和TACE的小分子抑制剂有治疗多种疾病的潜力。本发明提供了低分子量、非肽类的基质金属蛋白酶(MMPs)和TNF-α转化酶(TACE)抑制剂,用于治疗关节炎、肿瘤转移、组织溃疡、异常愈合、牙周病、骨病、糖尿病(胰岛素抵抗)和HIV感染,其化学式为1,其中R2和R3形成杂环环,A为S、S(O)或S(O)2,R1和R4如本文所定义。
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