(S)-1-methyl-1,2,3,6-hexahydro-[2,3']bipyridinyl | 5953-51-5

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: (S)-1-methyl-1,2,3,6-hexahydro-[2,3']bipyridinyl
• 英文别名: (S)-N-methylanatabine；N-methylanatabine；methylanatabine；(S)-1-Methyl-1,2,3,6-tetrahydro-[2,3']bipyridyl；(2S)-1-Methyl-1,2,3,6-tetrahydro-2,3'-bipyridine；3-[(2S)-1-methyl-3,6-dihydro-2H-pyridin-2-yl]pyridine
• CAS: 5953-51-5
• 化学式: C₁₁H₁₄N₂
• 分子量: 174.246
• InChiKey: ATWWUVUOWMJMTM-NSHDSACASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  16.1
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2933399090

反应信息

• 作为产物：
  描述：

  (S)-3,6-2H-[2,3']bipyridinyl-1-carboxylic acid 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 反应 6.0h， 以0.17 g的产率得到(S)-1-methyl-1,2,3,6-hexahydro-[2,3']bipyridinyl
  参考文献：
  名称：

  从烟草高效合成对吡咯烷和哌啶生物碱的对映体。

  摘要：

  对映体的六个哌啶和吡咯烷生物碱，（S）-去甲烟碱1，（S）-烟碱2，（S）-安那他滨3，（S）-N-甲基安那他滨4，（S）-天麻碱5和（S ）-N-甲基天麻碱6，是烟草中的天然产物，是由一种常见的手性均聚物（S）-3-（1-叠氮基-丁-3-烯基）-吡啶15建立的。该均聚物的分子内氢硼化-环烷基化叠氮化物中间体15是吡咯烷环形成中的关键步骤。二亚乙基胺中间体（S）-烯丙基-（1-吡啶-3-基-丁-3-烯基）-氨基甲酸苄酯20的闭环复分解反应（RCM）是哌啶环形成中的关键步骤。从市售的3-吡啶甲醛13中，描述了一种简便，简便的烟草生物碱对映体合成方法：（S）-去甲烟碱1（5个步骤，

  DOI：

  10.1021/jo010386b

文献信息

• [EN] 3-(1,2,3,6-TETRAHYDROPYRIDIN-2-YL)PYRIDINE GLUTARATE OR A PHARMACEUTICALLY ACCEPTABLE SOLVATE THEREOF<br/>[FR] 3- (1,2,3,6-TÉTRAHYDROPYRIDIN-2-YL) PYRIDINE GLUTARATE OU UN SOLVATE PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI
  申请人：PHILIP MORRIS PRODUCTS SA

  公开号：WO2020127225A1

  公开（公告）日：2020-06-25

  The present invention relates to 3 -( 1,2,3,6-tetrahydropyridin-2-yI)pyridine glutarate or a pharmaceutically acceptable solvate thereof, to a crystal thereof and to a polymorph of this crystal It further relates to the medicinal use of each of these, in particular in the treatment or prophylaxis of substance addiction or inflammation

  这项发明涉及3-(1,2,3,6-四氢吡啶-2-基)吡啶戊二酸盐或其药用可溶剂结晶体，以及该结晶体的多晶形态。此外，还涉及这些物质的药用，特别是在治疗或预防物质成瘾或炎症方面的用途。
• Stereoselectivity of the demethylation of nicotine piperidine homologues by Nicotiana plumbaginifolia cell suspension cultures
  作者：Trixie Ann Bartholomeusz、Roland Molinié、Albrecht Roscher、François-Xavier Felpin、Françoise Gillet、Jacques Lebreton、François Mesnard、Richard J. Robins

  DOI：10.1016/j.phytochem.2005.07.012

  日期：2005.8

  The metabolism of (R,S)-N-methylanabasine and (R,S)-N-methylanatabine has been studied in a cell suspension culture of Nicotiana plumbaginifolia. Both substrates are effectively demethylated, anabasine or anatabine, respectively, accumulating in the medium. Similarly, there is strong stereoselectivity for the (R)-isomers of both substrates. The kinetics of metabolism of (R,S)-N-methylanabasine differ significantly from those of nicotine in that no further degradation of the initial demethylation product occurs. (R,S)-N-Methylanatabine, however, shows kinetics closer to those of nicotine, with loss of alkaloid from the system. Furthermore, (R,S)-N-methylanabasine does not diminish (S)-nicotine demethylation, indicating a lack of competition. However, the metabolism of (S)-nicotine is affected by the presence of (R,S)-N-methylanabasine. Hence, the demethylation of the piperidine homologues of nicotine is seen to be similar but not identical to that of the pyridine analogues. The implications of these different metabolic profiles in relation to the demethylation activity are discussed. (c) 2005 Elsevier Ltd. All rights reserved.
• Spaeth; Kesztler, Chemische Berichte, 1937, vol. 70, p. 2450,2452
  作者：Spaeth、Kesztler

  DOI：——

  日期：——
• Efficient Enantiomeric Synthesis of Pyrrolidine and Piperidine Alkaloids from Tobacco
  作者：Felpin、Sandrine Girard、Giang Vo-Thanh、Richard J. Robins、Jean Villiéras、Jacques Lebreton

  DOI：10.1021/jo010386b

  日期：2001.9.1

  An enantiomeric synthesis of six piperidine and pyrrolidine alkaloids, (S)-nornicotine 1, (S)-nicotine 2, (S)-anatabine 3, (S)-N-methylanatabine 4, (S)-anabasine 5, and (S)-N-methylanabasine 6, known as natural products in tobacco, was established from a common chiral homoallylic (S)-3-(1-azido-but-3-enyl)-pyridine 15. An intramolecular hydroboration-cycloalkylation of the homoallylic azide intermediate

  对映体的六个哌啶和吡咯烷生物碱，（S）-去甲烟碱1，（S）-烟碱2，（S）-安那他滨3，（S）-N-甲基安那他滨4，（S）-天麻碱5和（S ）-N-甲基天麻碱6，是烟草中的天然产物，是由一种常见的手性均聚物（S）-3-（1-叠氮基-丁-3-烯基）-吡啶15建立的。该均聚物的分子内氢硼化-环烷基化叠氮化物中间体15是吡咯烷环形成中的关键步骤。二亚乙基胺中间体（S）-烯丙基-（1-吡啶-3-基-丁-3-烯基）-氨基甲酸苄酯20的闭环复分解反应（RCM）是哌啶环形成中的关键步骤。从市售的3-吡啶甲醛13中，描述了一种简便，简便的烟草生物碱对映体合成方法：（S）-去甲烟碱1（5个步骤，