N,N-dimethyl-1-(3-methyloxetan-3-yl)methanamine | 114644-08-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氧杂环丁烷
• 英文名称: N,N-dimethyl-1-(3-methyloxetan-3-yl)methanamine
• CAS: 114644-08-5
• 化学式: C₇H₁₅NO
• 分子量: 129.202
• InChiKey: HYXOMZVAPRMQFT-UHFFFAOYSA-N

物化性质

• 沸点：
  143.1±13.0 °C(Predicted)
• 密度：
  0.911±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  9
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  正丁基锂 、 N,N-dimethyl-1-(3-methyloxetan-3-yl)methanamine 在 水 、 重水 作用下， 生成 dimethyl-(2-methyl-2-hydroxymethyl-heptyl)-amine 、 3-deuterio-2-[(dimethylamino)methyl]-2-methylheptan-1-ol
  参考文献：
  名称：

  Enhanced reactivity of 3-(methoxymethyl)- and 3-(dimethylaminomethyl)oxetanes towards alkyllithiums

  摘要：

  DOI：

  10.1016/s0040-4039(00)96831-x
• 作为产物：
  描述：

  3-甲基-3-羟甲基氧杂环丁烷 以 乙醇 为溶剂， 反应 3.0h， 生成 N,N-dimethyl-1-(3-methyloxetan-3-yl)methanamine
  参考文献：
  名称：

  Enhanced reactivity of 3-(methoxymethyl)- and 3-(dimethylaminomethyl)oxetanes towards alkyllithiums

  摘要：

  DOI：

  10.1016/s0040-4039(00)96831-x

文献信息

• SUBSTITUTED THIOPHENYL URACILS, SALTS THEREOF AND THE USE THEREOF AS HERBICIDAL AGENTS
  申请人：Syngenta Crop Protection AG

  公开号：US20200315174A1

  公开（公告）日：2020-10-08

  The invention relates to substituted thiophenyl uracils of general formula (I) or the salts (I) thereof, wherein the groups in general formula (I) are as defined in the description, and to the use thereof as herbicides, in particular for controlling weeds and/or weed grasses in crops of cultivated plants and/or as plant growth regulators for influencing the growth of crops of cultivated plants.

  本发明涉及取代噻吩基尿嘧啶的通式(I)或其盐(I)，其中通式(I)中的基团如描述中定义，以及作为除草剂，特别是用于控制作物中的杂草和/或杂草草本的用途，以及作为植物生长调节剂用于影响栽培植物作物的生长。
• [EN] IMIDAZO(4,5-B)PYRIDINE-6-CARBOXAMIDES AS ANTI-INFLAMMATORY AGENTS<br/>[FR] IMIDAZO (4, 5 -B) PYRIDINE- 6 -CARBOXAMIDES EN TANT QU'AGENTS ANTI-INFLAMMATOIRES
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2012076674A1

  公开（公告）日：2012-06-14

  This invention relates to compounds of formula I their use as inhibitors of the microsomal prostaglandin E2 synthase-1 (mPGES-1), pharmaceutical compositions containing them, and their use as medicaments for the treatment and/or prevention of inflammatory diseases and associated conditions. A, L, M, W, R1, R2, R3, R4, R6, R7, Ra, Rb have meanings given in the description.

  这项发明涉及公式I化合物，它们作为微粒体前列腺素E2合酶-1（mPGES-1）的抑制剂的用途，含有它们的药物组合物，以及它们作为治疗和/或预防炎症性疾病和相关症状的药物的用途。A、L、M、W、R1、R2、R3、R4、R6、R7、Ra、Rb在描述中有给定的含义。
• NOVEL COMPOUNDS
  申请人：Priepke Henning

  公开号：US20120309755A1

  公开（公告）日：2012-12-06

  This invention relates to compounds of formula I their use as inhibitors of the microsomal prostaglandin E 2 synthase-1 (mPGES-1), pharmaceutical compositions containing them, and their use as medicaments for the treatment and/or prevention of inflammatory diseases and associated conditions. A, L, M, W, R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , R a , R b have meanings given in the description.

  这项发明涉及到I式化合物，它们作为微粒体前列腺素E2合酶-1（mPGES-1）的抑制剂的用途，含有它们的药物组合物，以及它们作为治疗和/或预防炎症性疾病及相关症状的药物的用途。A、L、M、W、R1、R2、R3、R4、R6、R7、Ra、Rb在描述中有给出它们的含义。
• [EN] GEM-DISUBSTITUTED PIPERIDINE MELANOCORTIN SUBTYPE-2 RECEPTOR (MC2R) ANTAGONISTS AND USES THEREOF<br/>[FR] ANTAGONISTES DU RÉCEPTEUR DU SOUS-TYPE 2 DE LA MÉLANOCORTINE (MC2R) À PIPÉRIDINE À DOUBLE SUBSTITUTION GEM ET LEURS UTILISATIONS
  申请人：CRINETICS PHARMACEUTICALS INC

  公开号：WO2021126693A1

  公开（公告）日：2021-06-24

  Described herein are compounds that are melanocortin subtype-2 receptor (MC2R) modulators, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders that would benefit from modulation of MC2R activity.

  本文描述了一些是黑色素皮质激素受体-2（MC2R）调节剂的化合物，制备这些化合物的方法，包括这些化合物的药物组合物和药物，以及使用这些化合物治疗需要调节MC2R活性的疾病、症状或疾病的方法。
• Substituted Heteroarylpiperidine Derivatives As Melanocortin-4 Receptor Modulators
  申请人：Henneböhle Marco

  公开号：US20100249093A1

  公开（公告）日：2010-09-30

  The present invention relates to substituted heteroarylpiperidine derivatives as melanocortin-4 receptor modulators. Depending on the structure and the stereochemistry the compounds of the invention are either selective agonists or selective antagonists of the human melanocortin-4 receptor (MC-4R). The agonists can be used for the treatment of disorders and diseases such as obesity, diabetes and sexual dysfunction, whereas the antagonists are useful for the treatment of disorders and diseases such as cancer cachexia, muscle wasting, anorexia, amyotrophic lateral sclerosis (ALS), anxiety and depression. Generally all diseases and disorders where the regulation of the MC-4R is involved can be treated with the compounds of the invention.

  本发明涉及取代杂环基哌啶衍生物作为黑色素-4受体调节剂。根据化合物的结构和立体化学，本发明的化合物可以是人类黑色素-4受体（MC-4R）的选择性激动剂或选择性拮抗剂。激动剂可用于治疗肥胖症、糖尿病和性功能障碍等疾病和疾病，而拮抗剂可用于治疗癌症消耗症、肌肉萎缩、厌食症、肌萎缩侧索硬化症（ALS）、焦虑和抑郁症等疾病和疾病。通常，涉及MC-4R调节的所有疾病和疾病都可以用本发明的化合物治疗。