N-(3-(diethylamino)propyl)hydrazinecarbothioamide | 28634-18-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: N-(3-(diethylamino)propyl)hydrazinecarbothioamide
• 英文别名: 1-Amino-3-[3-(diethylamino)propyl]thiourea
• CAS: 28634-18-6
• 化学式: C₈H₂₀N₄S
• 分子量: 204.34
• InChiKey: RHHBSDJAEVDHOK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  13
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  85.4
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-[3-(6(R,S)-bromo-5-oxo-6,7,8,9-tetrahydro-5H-benzocyclohepten-2-yl)-2-oxo-oxazolidin-5 (S)-ylmethyl]-acetamide 、 N-(3-(diethylamino)propyl)hydrazinecarbothioamide 以 乙醇 为溶剂， 生成 (S)-N-{3-[3-(3-diethylamino-propylamino)-1,4,5,6-tetrahydro-1,2-diaza-benzo[e]azulen-8-yl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide
  参考文献：
  名称：

  Synthesis and SAR of novel conformationally restricted oxazolidinones possessing Gram-positive and fastidious Gram-negative antibacterial activity. Part 2: Amino substitutions on heterocyclic D-ring system

  摘要：

  A novel series of conformationally restricted oxazolidinones was synthesized, in which the heterocyclic D ring was substituted with various amino groups. Several analogs exhibited potent activity against both Gram-positive and fastidious Gram-negative organisms. Certain aniino-substituted analogs also exhibited improved aqueous solubility compared to the corresponding un-substituted heterocyclic D-ring analogs.(c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.05.085
• 作为产物：
  描述：

  methyl (3-(diethylamino)propyl)carbamodithioate 在 一水合肼 作用下， 以 乙二醇甲醚 为溶剂， 生成 N-(3-(diethylamino)propyl)hydrazinecarbothioamide
  参考文献：
  名称：

  Synthesis and SAR of novel conformationally restricted oxazolidinones possessing Gram-positive and fastidious Gram-negative antibacterial activity. Part 2: Amino substitutions on heterocyclic D-ring system

  摘要：

  A novel series of conformationally restricted oxazolidinones was synthesized, in which the heterocyclic D ring was substituted with various amino groups. Several analogs exhibited potent activity against both Gram-positive and fastidious Gram-negative organisms. Certain aniino-substituted analogs also exhibited improved aqueous solubility compared to the corresponding un-substituted heterocyclic D-ring analogs.(c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.05.085

文献信息

• [EN] NEW 2-AMIDOTHIADIAZOLE DERIVATIVES<br/>[FR] NOUVEAUX DÉRIVÉS DE 2-AMIDOTHIADIAZOLE
  申请人：ALMIRALL SA

  公开号：WO2010043377A1

  公开（公告）日：2010-04-22

  New 2-amidothiadiazole derivatives having the chemical structure of formula (I) or pharmaceutically acceptable salts or N-oxides thereof as agonists of S1P1 receptors.

  新2-脒基噻二唑衍生物，具有公式(I)的化学结构，或其药用可接受的盐或N-氧化物，作为S1P1受体的激动剂。
• New 2-Amidothiadiazole Derivatives
  申请人：Almirall, S.A.

  公开号：EP2177521A1

  公开（公告）日：2010-04-21

  New 2-amidothiadiazole derivatives having the chemical structure of formula (I) or pharmaceutically acceptable salts or N-oxides thereof as agonists of S1P1 receptors.

  新的2-氨基噻二唑衍生物具有公式(I)的化学结构，或其药学上可接受的盐或N-氧化物，作为S1P1受体的激动剂。
• Antibacterial agents
  申请人：Boyer Earl Frederick

  公开号：US20050288273A1

  公开（公告）日：2005-12-29

  Compounds of formula I and methods for their preparation are disclosed. Further disclosed are methods of making biologically active compounds of formula I as well as pharmaceutically acceptable compositions comprising compounds of formula I. Compounds of formula I as disclosed herein can be used in a variety of applications including use as antibacterial agents.

  本文披露了I式化合物及其制备方法。此外，还披露了制备具有生物活性的I式化合物的方法，以及包含I式化合物的药学上可接受的组合物的方法。本文所披露的I式化合物可以用于多种应用，包括用作抗菌剂。
• NEW 2-AMIDOTHIADIAZOLE DERIVATIVES
  申请人：Grima Poveda Pedro Manuel

  公开号：US20110200557A1

  公开（公告）日：2011-08-18

  The present disclosure relates to 2-amidothiadiazole derivatives of formula (I) as well as pharmaceutical compositions comprising them, and their use in therapy as agonists of the S1P1 receptors.

  本公开涉及式(I)的2-氨基噻二唑衍生物，以及包含它们的药物组合物，并且它们在治疗中作为S1P1受体激动剂的用途。
• Synthesis of new alkylaminoalkyl thiosemicarbazones of 3-acetylindole and their effect on DNA synthesis and cell proliferation
  作者：T Siatra-Papastaikoudi、A Tsotinis、CP Raptopoulou、C Sambani、H Thomou

  DOI：10.1016/0223-5234(96)88215-8

  日期：1995.1

  The preparation of a number of thiosemicarbazones of 3-acetylindole is described. These compounds were evaluated in vitro for their effect on proliferation and cell-division delays in cultured human peripheral blood lymphocytes, and their effect on DNA synthesis in T-cell leukemia Molt-4 cells.