4-carbamothioylphenyl (S)-2-(6-methoxynaphthalen-2-yl)propanoate | 1000700-29-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 4-carbamothioylphenyl (S)-2-(6-methoxynaphthalen-2-yl)propanoate
• 英文别名: (S)-4-carbamothioylphenyl 2-(6-methoxynaphthalen-2-yl)propanoate,；otenaproxesul；Otenaproxesul；(4-carbamothioylphenyl) (2S)-2-(6-methoxynaphthalen-2-yl)propanoate
• CAS: 1000700-29-7
• 化学式: C₂₁H₁₉NO₃S
• 分子量: 365.453
• InChiKey: YCNMAPLPQYQJFC-ZDUSSCGKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  26
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  93.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  1-(6-methoxynaphthalen-2-yl)-N,N,N-trimethylethan-1-aminium trifluoromethanesulfonate 在 4-二甲氨基吡啶 、 锰 、 二氯化双(三环己基膦)镍(II) 、 (5aR,5a''R,6aR)-2',2',2''',2'''-tetramethyl-2,2''-bispiro[cyclopropa[4,5]cyclopenta[1,2-b]pyridine-6,5'-[1,3]dioxane] 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 2-甲基四氢呋喃 、 甲醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 28.0h， 生成 4-carbamothioylphenyl (S)-2-(6-methoxynaphthalen-2-yl)propanoate
  参考文献：
  名称：

  由手性 2,2'-联吡啶配体实现的镍催化对映收敛羧基化

  摘要：

  使用 CO 2的对映选择性羧化反应已被证明可有效合成手性羧酸，包括普罗芬家族抗炎药。该反应在大气压力下进行，并受益于使用镍催化结合手性 2,2'-联吡啶配体（即 Me-Sbpy）的温和条件。

  DOI：

  10.1002/anie.202213943

文献信息

• Syntheses, toxicities and anti-inflammation of H 2 S-donors based on non-steroidal anti-inflammatory drugs
  作者：Meng Li、Jili Li、Taofeng Zhang、Quanyi Zhao、Jie Cheng、Bin Liu、Zhen Wang、Libo Zhao、Chenwei Wang

  DOI：10.1016/j.ejmech.2017.06.012

  日期：2017.9

  Three series of H2S donors based on NSAIDs were synthesized and characterized by H-1-NMR, IR and ESIHRMS. The H2S-release abilities of all compounds were evaluated in the presence of TECP or cysteine. The results show all compounds were fast H2S-releasers, and their half-lives were in range of 0-20 min. Under the same condition, H2S released from compound 9 was more than any other compounds. In cytotoxicity aspect, all compounds but 1 and 2 displayed much lower toxicities to both LO2 and HepG2 cell lines, and the IC50 values of most compounds were over 800 mu M. Compounds 1 and 2 had a stronger anti-proliferative activity to both cell lines, but they displayed lower toxicities to LO2 than to HepG2. Based on the cytotoxicity, the developmental toxicities of the compounds were assessed using zebrafish embryos. The results show all tested compounds 2, 9 and 15 had effects on the mortality, hatching rate and spontaneous movements of zebrafish embryos, and caused embryos teratogenesis; and the compounds had dose-dependent toxicities to both embryonic and larval zebrafish. In addition, all compounds had a better anti-inflammatory activity. In the test of anti-inflammatory activities, the tested compounds all reduced the levels of intracellular nitrite and pro-inflammatory cytokines (TNF-alpha, COX-2), increased the levels of anti-inflammatory cytokines (IL-10, HO-1). All these suggest these H2S donors based on NSAIDs have a potential to be a candidate medicine. (C) 2017 Elsevier Masson SAS. All rights reserved.
• COMPOUNDS FOR THIOL-TRIGGERED COS AND/OR H2S RELEASE AND METHODS OF MAKING AND USING THE SAME
  申请人：University of Oregon

  公开号：US20210214368A1

  公开（公告）日：2021-07-15

  Disclosed herein are embodiments of a compound that is capable of releasing COS and/or H 2 S upon reaction with a thiol-containing compound. The compound embodiments also can produce a detectable signal (e.g., a fluorescent signal) substantially concomitantly with COS and/or H 2 S release and/or can release an active agent, such as a therapeutic agent. Methods of making and using the compound embodiments also are disclosed.
• Nickel‐Catalyzed Enantioconvergent Carboxylation Enabled by a Chiral 2,2′‐Bipyridine Ligand
  作者：Linghua Wang、Tao Li、Saima Perveen、Shuai Zhang、Xicheng Wang、Yizhao Ouyang、Pengfei Li

  DOI：10.1002/anie.202213943

  日期：2022.12.19

  An enantioselective carboxylation reaction using CO2 has been demonstrated as efficient for the synthesis of chiral carboxylic acids including profen family anti-inflammatory drugs. The reaction takes place under atmospheric pressure and benefits from mild conditions using nickel-catalysis in combination with a chiral 2,2′-bipyridine ligand, namely Me-Sbpy.

  使用 CO 2的对映选择性羧化反应已被证明可有效合成手性羧酸，包括普罗芬家族抗炎药。该反应在大气压力下进行，并受益于使用镍催化结合手性 2,2'-联吡啶配体（即 Me-Sbpy）的温和条件。