ethyl-(1-methyl-1H-pyrazol-3-ylmethyl)-amine | 952194-96-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: ethyl-(1-methyl-1H-pyrazol-3-ylmethyl)-amine
• 英文别名: N-[(1-methylpyrazol-3-yl)methyl]ethanamine
• CAS: 952194-96-6
• 化学式: C₇H₁₃N₃
• 分子量: 139.2
• InChiKey: JAEGNPQVVDHAID-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0
• 重原子数：
  10
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  29.8
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  ethyl-(1-methyl-1H-pyrazol-3-ylmethyl)-amine 、 [(2-chloro-5-dimethylamino-phenyl)-(3,4-dimethoxy-benzenesulfonyl)-amino]-acetic acid 在 benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 2-[(2-Chloro-5-dimethylamino-phenyl)-(3,4-dimethoxy-benzenesulfonyl)-amino]-N-ethyl-N-(1-methyl-1H-pyrazol-3-ylmethyl)-acetamide
  参考文献：
  名称：

  N-Glycine-sulfonamides as potent dual orexin 1/orexin 2 receptor antagonists

  摘要：

  A series of dual OX(1)R/OX(2)R orexin antagonists was prepared based on a N-glycine-sulfonamide core. SAR studies of a screening hit led to compounds with low nanomolar affinity for both receptors and good oral bioavailability. One of these compounds, 47, has demonstrated in vivo activity in rats following oral administration. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.09.079
• 作为产物：
  描述：

  1-甲基-1H-吡唑-3-甲醛 、 乙胺 以 四氢呋喃 为溶剂， 生成 ethyl-(1-methyl-1H-pyrazol-3-ylmethyl)-amine
  参考文献：
  名称：

  NOVEL SULFONAMIDE COMPOUNDS

  摘要：

  本发明涉及新型磺酰胺化合物及其作为促进睡眠荷尔蒙受体拮抗剂的用途。

  公开号：

  US20090275588A1

文献信息

• NOVEL SULFONAMIDE COMPOUNDS
  申请人：Aissaoui Hamed

  公开号：US20090275588A1

  公开（公告）日：2009-11-05

  The invention relates to novel sulfonamide compounds and their use as orexin receptor antagonists.

  这项发明涉及新型磺胺类化合物及其作为促觉醒素受体拮抗剂的用途。
• BIARYL AMIDE DERIVATIVE OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
  申请人：Katayama Seiji

  公开号：US20130116227A1

  公开（公告）日：2013-05-09

  Disclosed is a novel biaryl amide derivative represented by formula (1) and having an affinity for the aldosterone receptor; also disclosed is a pharmaceutically acceptable salt thereof. (In the formula, A is any of the groups represented by formula (a); L is —CONH—, etc.; R 1 is a substitutable aminosulfonyl group, etc.; R 2 is a hydrogen atom, etc.; R 3 is a hydrogen atom, etc.; R 4 is a hydrogen atom, a halogen atom, hydroxy group, a substitutable amino group, a substitutable C 1-6 alkoxy group, a substitutable 4- to 7-membered cyclic amino group, etc.; R 5a , R 5b and R 5c are each independently hydrogen atoms, etc.; R 6 is a halogen atom, a cyano group, etc.; R 7 and R 8 are each independently a hydrogen atom, etc.; and m is an integer such as 0.)

  揭示了一种表示为公式（1）的新型联苯酰胺衍生物，具有与醛固酮受体的亲和力；还揭示了其药用可接受的盐。（在该公式中，A是由公式（a）表示的任何基团之一；L是—CONH—等；R1是可替代的氨基磺酰基等；R2是氢原子等；R3是氢原子等；R4是氢原子、卤原子、羟基、可替代的氨基基团、可替代的C1-6烷氧基、可替代的4-到7-成员环氨基基团等；R5a、R5b和R5c各自独立地是氢原子等；R6是卤原子、氰基等；R7和R8各自独立地是氢原子等；m是整数，例如0。）
• US8003654B2
  申请人：——

  公开号：US8003654B2

  公开（公告）日：2011-08-23
• [EN] NOVEL SULFONAMIDE COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS SULFONAMIDES
  申请人：ACTELION PHARMACEUTICALS LTD

  公开号：WO2007116374A1

  公开（公告）日：2007-10-18

  [EN] The invention relates to sulfonamide compounds of formula (I), where A, B, R³ and R⁴ are as defined in the claims, and their use as orexin receptor antagonists in the prevention and treatment of eating and drinking disorders, all types of sleep disorders, all kinds of cognitive dysfunctions in the healthy population and psychiatric and neurologic disorders. Formula (I).
  [FR] L'invention concerne de nouveaux composés sulfonamides correspondant à la formule (I) dans laquelle A, B, R³ et R⁴sont définis dans les revendications et leur utilisation en tant qu'antagonistes des récepteurs de l'orexine, utilisés dans la prévention et le traitement de troubles de l'alimentation et d'absorption de liquides, de tous types de troubles du sommeil, des dysfonctionnements cognitifs en tous genres dans une population en bonne santé et de troubles psychiatriques ou neurologiques.
• N-Glycine-sulfonamides as potent dual orexin 1/orexin 2 receptor antagonists
  作者：Hamed Aissaoui、Ralf Koberstein、Cornelia Zumbrunn、John Gatfield、Catherine Brisbare-Roch、Francois Jenck、Alexander Treiber、Christoph Boss

  DOI：10.1016/j.bmcl.2008.09.079

  日期：2008.11

  A series of dual OX(1)R/OX(2)R orexin antagonists was prepared based on a N-glycine-sulfonamide core. SAR studies of a screening hit led to compounds with low nanomolar affinity for both receptors and good oral bioavailability. One of these compounds, 47, has demonstrated in vivo activity in rats following oral administration. (C) 2008 Elsevier Ltd. All rights reserved.