N,S-dimethyl-N-phenylthiohydroxylamine | 65605-22-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N,S-dimethyl-N-phenylthiohydroxylamine
• 英文别名: N-Methylmethansulfenanilid；N-methyl-N-methylsulfanylaniline
• CAS: 65605-22-3
• 化学式: C₈H₁₁NS
• 分子量: 153.248
• InChiKey: PQIMABKJRVMGOA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  10
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  28.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N,S-dimethyl-N-phenylthiohydroxylamine 在 silver hexafluoroantimonate 作用下， 以 氯苯 为溶剂， 以23 %的产率得到N-methyl-4-(methylthio)aniline
  参考文献：
  名称：

  银催化 N-磺基苯胺的对位选择性磺基转移反应

  摘要：

  银催化剂在温和的反应条件下有效促进了N-磺基苯胺的对位选择性重排反应。 该反应通过硫基的分子间转移进行。

  DOI：

  10.1002/chem.202301751
• 作为产物：
  描述：

  1-methoxydichloromethyl-2-methyldisulphane 、 N-甲基苯胺 生成 N,S-dimethyl-N-phenylthiohydroxylamine
  参考文献：
  名称：

  BARANY, G., TETRAHEDRON LETT., 1983, 24, N 51, 5683-5686

  摘要：

  DOI：

文献信息

• [EN] HYBRID MU OPIOID RECEPTOR AND NEUROPEPTIDE FF RECEPTOR BINDING MOLECULES, THEIR METHODS OF PREPARATION AND APPLICATIONS IN THERAPEUTIC TREATMENT<br/>[FR] RÉCEPTEUR D'OPIOÏDE MU HYBRIDE ET MOLÉCULES DE LIAISON DE RÉCEPTEUR DE NEUROPEPTIDE FF, LEURS PROCÉDÉS DE PRÉPARATION ET D'APPLICATIONS DANS UN TRAITEMENT THÉRAPEUTIQUE
  申请人：CENTRE NAT RECH SCIENT

  公开号：WO2019170919A1

  公开（公告）日：2019-09-12

  The present invention relates to molecules binding the mu opioid receptor (MOR) and the neuropeptide FF receptor (NPFFR) and in particular molecules having a MOR agonist and NPFFR modulatory activity. The present invention relates to pharmaceutical compositions, and in particular useful in the treatment of pain and/or hyperalgesia.

  本发明涉及结合μ阿片受体（MOR）和神经肽FF受体（NPFFR）的分子，特别是具有MOR激动剂和NPFFR调节活性的分子。本发明涉及药物组合物，特别是在治疗疼痛和/或过敏症方面有用。
• Cyclopenta[d]pyrimidines And Substituted Cyclopenta[d]pyrimidines As Antitubulin and Microtubule Targeting Agents, Monocyclic Pyrimidines As Tubulin Inhibitors, And Pyrrolopyrimidines As Targeted Antifolates And Tubulin and Multiple Receptor Tyrosine Kinase Inhibition And Antitumor Agents
  申请人：Duquesne University of the Holy Spirit

  公开号：US20160304525A1

  公开（公告）日：2016-10-20

  The present invention provides a compound of Formula I, and salts thereof, and a pharmaceutical composition comprising a compound of Formula I: wherein R 1 is selected from the group consisting of and R 2 is an alkyl group having from one to ten carbon atoms, or wherein R 2 is selected from the group consisting of R 1 is an alkyl group having from one to ten carbon atoms; and R is H, or an alkyl group having from one to ten carbon atoms, and R 3 is H, an alkyl group having from one to ten carbon atoms, or a halogen. Preferably the compound of Formula V includes wherein R 3 is a halogen, and most preferably wherein the halogen is chlorine. Methods of treating a patient with cancer with these compounds are also provided.

  本发明提供了一种化合物I的盐，以及包括化合物I的药物组合物：其中R1选自以下组成的群体，R2是具有一到十个碳原子的烷基基团，或者R2选自以下组成的群体，R1是具有一到十个碳原子的烷基基团；R是H，或者具有一到十个碳原子的烷基基团，R3是H，具有一到十个碳原子的烷基基团，或者卤素。优选化合物V包括其中R3是卤素，最优选其中卤素是氯。还提供了使用这些化合物治疗癌症患者的方法。
• Cyclopenta[d]pyrimidines and substituted cyclopenta[d]pyrimidines as antitubulin and microtubule targeting agents, monocyclic pyrimidines as tubulin inhibitors, and pyrrolopyrimidines as targeted antifolates and tubulin and multiple receptor tyrosine kinase inhibition and antitumor agents
  申请人：Duquesne University of the Holy Spirit

  公开号：US10239880B2

  公开（公告）日：2019-03-26

  The present invention provides a compound of Formula I, and salts thereof, and a pharmaceutical composition comprising a compound of Formula I: wherein R1 is selected from the group consisting of and R2 is an alkyl group having from one to ten carbon atoms, or wherein R2 is selected from the group consisting of R1 is an alkyl group having from one to ten carbon atoms; and R is H, or an alkyl group having from one to ten carbon atoms, and R3 is H, an alkyl group having from one to ten carbon atoms, or a halogen. Preferably the compound of Formula V includes wherein R3 is a halogen, and most preferably wherein the halogen is chlorine. Methods of treating a patient with cancer with these compounds are also provided.

  本发明提供了一种式 I 的化合物及其盐类，以及一种包含式 I 化合物的药物组合物： 其中 R1 选自以下组成的组 和 R2 是具有 1 至 10 个碳原子的烷基，或 其中 R2 选自以下组成的组 R1 是具有一至十个碳原子的烷基；R 是 H 或具有一至十个碳原子的烷基，R3 是 H、具有一至十个碳原子的烷基或卤素。其中 R3 是卤素，最优选的是卤素是氯。还提供了用这些化合物治疗癌症患者的方法。
• Cyclopenta[d]pyrimidines and substituted cyclopenta[d]pyrimidines as antitubulin and microtubule targeting agents, monocyclic pyrimidines as tubulin inhibitors, and pyrrolopyrimidines as targeted antifolates and tubulin and multiple receptor tyrosine kinase inhibitor and antitumor agents
  申请人：Duquesne University of the Holy Spirit

  公开号：US11124520B2

  公开（公告）日：2021-09-21

  The present invention provides a compound of Formula III, and salts thereof, and a pharmaceutical composition comprising a compound of Formula III: wherein R1 is selected from the group consisting of: wherein R2 is H or an alkyl group having from one to ten carbon atoms; R3 is H or an alkyl group having from one to ten carbon atoms; and R4 is H or an alkyl group having from one to ten carbon atoms. Methods of treating a patient with cancer with these compounds are also provided.

  本发明提供了一种式 III 的化合物及其盐类，以及一种包含式 III 化合物的药物组合物： 其中 R1 选自以下组成的组 在其中 R2 是 H 或具有一至十个碳原子的烷基； R3 是 H 或具有一至十个碳原子的烷基；以及 R4 是 H 或具有一至十个碳原子的烷基。还提供了用这些化合物治疗癌症患者的方法。
• BARANY, G.;SCHROLL, A. L.;MOTT, A. W.;HALSRUD, D. A., J. ORG. CHEM., 1983, 48, N 24, 4750-4761
  作者：BARANY, G.、SCHROLL, A. L.、MOTT, A. W.、HALSRUD, D. A.

  DOI：——

  日期：——