trans-2-Methyl-6-(1-pyrrolidinylmethyl)piperidine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: trans-2-Methyl-6-(1-pyrrolidinylmethyl)piperidine
• 英文别名: (2R,6S)-2-methyl-6-(pyrrolidin-1-ylmethyl)piperidine
• 化学式: C₁₁H₂₂N₂
• 分子量: 182.309
• InChiKey: GYERECBWVQFHTG-MNOVXSKESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  15.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3,4-二氯苯乙酸 、 trans-2-Methyl-6-(1-pyrrolidinylmethyl)piperidine 在 N,N'-羰基二咪唑 作用下， 生成 哌啶,1-[(3,4-二氯苯基)乙酰基]-2-甲基-6-(1-吡咯烷基甲基)-,反-
  参考文献：
  名称：

  New .kappa.-receptor agonists based upon a 2-[(alkylamino)methyl]piperidine nucleus

  摘要：

  The syntheses of some 1-[(3,4-dichlorophenyl)acetyl]2-[(alkylamino)methyl]peperidines and their activities as kappa-opioid receptor agonists are described. Selected structural modifications are made to the basic moiety and at the 2-, 3-, 4-, 5-, and 6-positions on the piperidine nucleus to enable structure-activity relationships to be delineated. As a result, some highly potent and selective kappa-receptor agonists have been identified. In particular, this has been achieved by introduction of oxygen-containing functionality into the 4-position of the piperidine nucleus or the 3-position of the pyrrolidinylmethyl side chain. Thus, 1-[(3,4-dichlorophenyl)acetyl]2-[[1-(3-oxopyrrolidinyl)methyl]?? piperidine (10) possesses high activity in the rabbit vas deferens (LCD, kappa-specific tissue) (IC50 = 0.20 nM) and is a potent antiociceptive agent, as determined by the mouse acetylcholine-induced abdominal constriction test (MAC) (ED50 = 0.06 mg/kg sc). The spirocyclic analogue 8-[3,4-dichlorophenyl)acetyl]7-(1-pyrrolidinylmethyl)-1,4-dioxa-8-azaspiro[4.5]decane (39) showed exceptionally potent activity: LVD, IC50 = 0.10 nM; MAC, ED50 = 0.001 mg/kg, sc. Both 10 and 39 displayed high selectivity for kappa-opioid receptors over both mu- and delta-opioid receptor subtypes.

  DOI：

  10.1021/jm00081a009
• 作为产物：
  描述：

  6-甲基-2-吡啶甲醛 以 乙醇 、 二氯甲烷 、 溶剂黄146 为溶剂， 生成 trans-2-Methyl-6-(1-pyrrolidinylmethyl)piperidine
  参考文献：
  名称：

  Piperidine derivatives

  摘要：

  披露了公式(I)的化合物，其中 R₁代表羟基，C₁₋₆烷基，C₁₋₆羟烷基，C₁₋₆羧烷基，苯基，氧代，氨基，羧基，酰胺，-NR₄COR₅（其中R₄和R₅都代表C₁₋₆烷基），可选地取代的亚甲基，或者与它连接的碳原子一起，R₁形成一个含有一个或多个杂原子的5或6元环； R₂和R₃相同或不同，是C₁₋₆烷基或C₃₋₆烯丙基；或者-NR₂R₃形成一个5元环（可选地含有与氮原子相邻的氧原子）或6元环，该环可选地含有一个不饱和单元，并且该环未取代或被羟基，氧代，可选地取代的亚甲基，-COR₆（其中R₆代表C₁₋₆烷基，OR₇或-NHR₇，R₇代表氢，C₁₋₆烷基，芳基，芳(C₁₋₆)烷基）或=NOR₈（其中R₈代表C₁₋₆烷基）取代； X代表直接键，-CH₂-或-CH₂O-； Ar代表取代的苯基部分； 以及它们的生理可接受盐。 这些化合物被指出用于治疗疼痛和脑缺血。还披露了它们的制备过程和中间体以及含有它们的药物组合物。

  公开号：

  EP0330461A3

文献信息

• Spiropiperidine derivatives
  申请人：Glaxo Group Limited

  公开号：US05114945A1

  公开（公告）日：1992-05-19

  Compounds are disclosed of formula (I) ##STR1## wherein R.sub.1 represents hydroxy, C.sub.1-6 alkyl, C.sub.1-6 hydroxyalkyl, C.sub.1-6 carboxyalkyl, phenyl, oxo, amino, carboxy, amido, --NR.sub.4 COR.sub.5 (where R.sub.4 and R.sub.5 both represent C.sub.1-6 alkyl), optionally substituted methylidene or, together with the carbon atom to which it is attached, R.sub.1 forms a 5 or 6-membered ring containing one or more heteroatoms; R.sub.2 and R.sub.3 are the same or different and are C.sub.1-6 alkyl or C.sub.3-6 alkenyl; or --NR.sub.2 R.sub.3 forms a 5-membered (optionally containing an oxygen atom adjacent to the nitrogen) or a 6-membered ring, which ring optionally contains one unit of unsaturation and which is unsubstituted or substituted by hydroxy, oxo, optionally substituted methylidene, --COR.sub.6 (where R.sub.6 represents C.sub.1-6 alkyl, OR, or --NHR, and R represents hydrogen, C.sub.1-6 alkyl, aryl, ar(C.sub.1-6)alkyl) or .dbd.NOR.sub.8 (where R.sub.8 represents C.sub.1-6 alkyl); X represents a direct bond, --CH.sub.2 -- or --CH.sub.2 0--; Ar represents a substituted phenyl moiety; and physiologically acceptable salts thereof. The compounds are indicated as useful for the treatment of pain and cerebral ischemia. Proccesses and intermediates for their preparation and pharmaceutical compositions containing them are also disclosed.

  披露了公式(I)的化合物##STR1##，其中R1代表羟基，C1-6烷基，C1-6羟烷基，C1-6羧烷基，苯基，氧代，氨基，羧基，酰胺基，--NR4COR5（其中R4和R5都代表C1-6烷基），可选地取代亚甲基，或者与它连接的碳原子一起，R1形成一个含有一个或多个杂原子的5或6元环；R2和R3相同或不同，是C1-6烷基或C3-6烯基；或者--NR2R3形成一个5元环（可选地含有一个靠近氮原子的氧原子）或6元环，该环可选地含有一个不饱和单元，并且该环未取代或被羟基，氧代，可选地取代亚甲基，--COR6（其中R6代表C1-6烷基，OR或--NHR，R代表氢，C1-6烷基，芳基，芳(C1-6)烷基）或.dbd.NOR8（其中R8代表C1-6烷基）取代；X代表直接键，--CH2--或-- O--; Ar代表一个取代的苯基部分；以及它们的生理学可接受盐。这些化合物被指出用于治疗疼痛和脑缺血。还披露了它们的制备过程和中间体以及含有它们的药物组合物。
• US5114945A
  申请人：——

  公开号：US5114945A

  公开（公告）日：1992-05-19