(2S)-2-((dimethylamino)methyl)pyrrolidine-1-carboxylic acid tert-butyl ester | 160115-24-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: (2S)-2-((dimethylamino)methyl)pyrrolidine-1-carboxylic acid tert-butyl ester
• 英文别名: (S)-tert-butyl 2-((dimethylamino)methyl)pyrrolidine-1-carboxylate；tert-butyl (2S)-2-[(dimethylamino)methyl]pyrrolidine-1-carboxylate
• CAS: 160115-24-2
• 化学式: C₁₂H₂₄N₂O₂
• 分子量: 228.335
• InChiKey: CNVUYXYLHUYWKR-JTQLQIEISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  32.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (2S)-2-((dimethylamino)methyl)pyrrolidine-1-carboxylic acid tert-butyl ester 在 盐酸 、 N-羟基-7-氮杂苯并三氮唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三氟乙酸 作用下， 以 二氯甲烷 、 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 反应 162.82h， 生成 {(E)-4-[((R)-1-{[(R)-1-Benzyl-2-((S)-3-dimethylaminomethyl-pyrrolidin-1-yl)-2-oxo-ethyl]-methyl-carbamoyl}-2-naphthalen-2-yl-ethyl)-methyl-carbamoyl]-1,1-dimethyl-but-3-enyl}-carbamic acid tert-butyl ester
  参考文献：
  名称：

  The influence of conformational restriction in the C-terminus of growth hormone secretagogues on their potency

  摘要：

  in order to obtain more potent growth hormone secretagogues, a comparison of ipamorelin and NN703 suggested the addition of a polar group at the C-terminus of NN703. A study was conducted using constrained amines for this purpose. Here, substituted 4-piperidinylamino- and 4-dimethylaminopiperidino-substitutents were found to give the most active compounds. A replacement of the 4-dimethylaminopiperidino-substituent with 4-hydroxypiperidino resulted in a series of compounds, which showed in vitro activity with EC50 values in the low nanomolar range, and favourable kinetic properties, such as 40% oral bioavailability. The most promising compound was also tested in a swine in vivo model, resulting in a growth hormone level with a C-max of over 40 ng mL(-1). (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved..

  DOI：

  10.1016/s0223-5234(02)01370-3
• 作为产物：
  描述：

  (S)-1-tert-butyl 2-ethylpyrrolidine-1,2-dicarboxylate 在 4 A molecular sieve 、 三乙酰氧基硼氢化钠 、 二异丁基氢化铝 、 溶剂黄146 作用下， 以 乙醚 、 乙醇 、 二氯甲烷 、 甲苯 为溶剂， 反应 78.0h， 生成 (2S)-2-((dimethylamino)methyl)pyrrolidine-1-carboxylic acid tert-butyl ester
  参考文献：
  名称：

  The influence of conformational restriction in the C-terminus of growth hormone secretagogues on their potency

  摘要：

  in order to obtain more potent growth hormone secretagogues, a comparison of ipamorelin and NN703 suggested the addition of a polar group at the C-terminus of NN703. A study was conducted using constrained amines for this purpose. Here, substituted 4-piperidinylamino- and 4-dimethylaminopiperidino-substitutents were found to give the most active compounds. A replacement of the 4-dimethylaminopiperidino-substituent with 4-hydroxypiperidino resulted in a series of compounds, which showed in vitro activity with EC50 values in the low nanomolar range, and favourable kinetic properties, such as 40% oral bioavailability. The most promising compound was also tested in a swine in vivo model, resulting in a growth hormone level with a C-max of over 40 ng mL(-1). (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved..

  DOI：

  10.1016/s0223-5234(02)01370-3

文献信息

• [EN] Novel pyrido[2,3-b]indole compounds for the treatment and prophylaxis of bacterial infection<br/>[FR] NOUVEAUX COMPOSÉS PYRIDO[2,3-B]INDOLE POUR LE TRAITEMENT ET LA PROPHYLAXIE D'UNE INFECTION BACTÉRIENNE
  申请人：HOFFMANN LA ROCHE

  公开号：WO2018178041A1

  公开（公告）日：2018-10-04

  The present invention relates to novel compounds of formula (I), wherein R1, R2, R3, R4, R5 and R6 are as described herein, and their pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions including the compounds and methods of using the compounds.

  本发明涉及式(I)的新化合物，其中R1、R2、R3、R4、R5和R6如本文所述，以及它们的药用盐、对映体或二对映体，以及包括这些化合物的组合物和使用这些化合物的方法。
• An enantioselective Michael addition of soft nucleophiles to prochiral enone catalyzed by (2-pyrrolidyl)alkyl ammonium hydroxide
  作者：Akihiro Kawara、Takeo Taguchi

  DOI：10.1016/s0040-4039(00)78503-0

  日期：1994.11

  (S)-N-(2-Pyrrolidylmethyl)-N,N,N-trimethylammonium hydroxide catalyzes the asymmetric Michael addition of soft nucleophiles to enones with moderate to high enantiomeric excess through ion-pair rather than steric control.

  （S）-N-（2-吡咯烷基甲基）-N，N，N-三甲基氢氧化铵通过离子对而非空间控制，将软亲核试剂不对称迈克尔加成到中度至高对映体过量的烯酮上。
• Compounds with growth hormone releasing properties
  申请人：Peschke Bernd

  公开号：US06919315B1

  公开（公告）日：2005-07-19

  Disclosed are compounds of formula I formula I wherein R 1 , R 2 , R 5 , R 6 , R 7 , R 8 , G, J, L, M, a, b, c, d, e, and f are as defined in the specification, and compositions containing them. These compounds are useful for treating medical disorders resulting from a deficiency in growth hormone.

  揭示了具有公式I的化合物，其中R1、R2、R5、R6、R7、R8、G、J、L、M、a、b、c、d、e和f如规范中定义，并含有它们的组合物。这些化合物可用于治疗由生长激素缺乏引起的医学疾病。
• [EN] COMPOUNDS WITH GROWTH HORMONE RELEASING PROPERTIES<br/>[FR] COMPOSES A PROPRIETES DE LIBERATION DE L'HORMONE DE CROISSANCE
  申请人：NOVO NORDISK AS

  公开号：WO2000001726A1

  公开（公告）日：2000-01-13

  The invention relates to novel compounds, compositions containing them, and their use for treating medical disorders resulting from a deficiency in growth hormone.

  该发明涉及新型化合物、含有它们的组合物以及它们用于治疗由生长激素缺乏引起的医疗障碍的用途。
• Antifungal bicyclic hetero ring compounds
  申请人：Daiichi Sankyo Company, Limited

  公开号：US07737166B2

  公开（公告）日：2010-06-15

  A 1,6-β-glucan synthetase inhibitor is provided, having potent growth inhibition and having excellent safety. A compound is provided, capable of expressing in a wide spectral range and specifically or selectively, an antifungal effect based on its functional mechanism of 1,6-β-glucan synthesis inhibition. Also provided is a drug, a salt or hydrate thereof, especially an antifungal that contains the compound. Concretely, provided is a compound of the following formula (I), its salt or hydrate, and a drug or antifungal containing, as the active ingredient, the compound, its salt or hydrate:

  提供了一种1,6-β-葡聚糖合成酶抑制剂，具有强效的生长抑制作用和优异的安全性。提供了一种化合物，能够在广泛的光谱范围内表达，并基于其1,6-β-葡聚糖合成抑制的功能机制，具有特异性或选择性的抗真菌作用。此外，还提供了一种药物、其盐或水合物，特别是含有该化合物的抗真菌药物。具体而言，提供了以下式（I）的化合物、其盐或水合物，以及含有该化合物、其盐或水合物作为活性成分的药物或抗真菌药物：