benzyl-(4-isocyanato-pyridin-2-yl)-methyl-amine | 462070-64-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: benzyl-(4-isocyanato-pyridin-2-yl)-methyl-amine
• 英文别名: 2-(Benzyl-methyl-amino)-4-isocyanato-pyridine；N-benzyl-4-isocyanato-N-methylpyridin-2-amine
• CAS: 462070-64-0
• 化学式: C₁₄H₁₃N₃O
• 分子量: 239.277
• InChiKey: BDCOESSGNHGZTD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  45.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-(2-aminoethyl)-4-benzylpiperidin-4-ol 、 benzyl-(4-isocyanato-pyridin-2-yl)-methyl-amine 生成 1-[2-(4-Benzyl-4-hydroxy-piperidin-1-yl)-ethyl]-3-[2-(benzyl-methyl-amino)-pyridin-4-yl]-urea
  参考文献：
  名称：

  Quinoline derivatives

  摘要：

  本发明涉及新型1-吡啶-4-基脲衍生物及相关化合物，以及它们作为制备药物组合物的活性成分的用途。本发明还涉及相关方面，包括制备化合物的过程，含有这些化合物中的一种或多种的制药组合物，特别是它们作为神经激素拮抗剂的用途。

  公开号：

  US07375227B2

文献信息

• [EN] 4-(PIPERIDYL- AND PYRROLIDYL-ALKYL-UREIDO) -QUINOLINES AS UROTENSIN II RECEPTOR ANTAGONISTS<br/>[FR] NOUVEAUX DERIVES DE QUINOLEINES
  申请人：ACTELION PHARMACEUTICALS LTD

  公开号：WO2003048154A1

  公开（公告）日：2003-06-12

  The invention relates to novel 1-pyridin-4-yl urea derivatives and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as neurohormonal antagonists.

  本发明涉及新型的1-吡啶-4-基脲衍生物及相关化合物，以及它们作为制备药物组合物的活性成分的用途。本发明还涉及相关方面，包括制备这些化合物的过程，含有这些化合物中的一个或多个的药物组合物，特别是它们作为神经荷尔蒙拮抗剂的用途。
• 1-Pyridin-4-yl-urea derivatives
  申请人：Aissaoui Hamed

  公开号：US20060094716A1

  公开（公告）日：2006-05-04

  The invention relates to novel 1-pyridin-4-yl urea derivatives and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as neurohormonal antagonists.

  本发明涉及新型的1-吡啶-4-基脲衍生物及其相关化合物，以及将其用作制备药物组合物中的活性成分。本发明还涉及相关方面，包括制备该化合物的过程，含有其中一个或多个化合物的药物组合物，特别是它们作为神经激素拮抗剂的用途。
• 1,2,3,4-tetrahydroisoquinolines derivatives
  申请人：——

  公开号：US20040242564A1

  公开（公告）日：2004-12-02

  The invention relates to novel 1,2,3,4-tetrahydroisoquinoline derivatives and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as neurohormonal antagonists.

  本发明涉及新型1,2,3,4-四氢异喹啉衍生物及相关化合物，以及它们作为制备药物组成部分的活性成分的用途。本发明还涉及相关方面，包括制备化合物的过程，含有其中一种或多种化合物的药物组成物，特别是它们作为神经荷尔蒙拮抗剂的用途。
• 1 2 3 4 Tetrahydroisoquinolines derivatives as urotensin II receptor antagonists
  申请人：——

  公开号：US20040110744A1

  公开（公告）日：2004-06-10

  The invention relates to novel 1,2,3,4-tetrahydroisoquinoline derivatives of formula (I) and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as neurohormonal antagonists especially urotensin II antagonists.

  本发明涉及一种新型1,2,3,4-四氢异喹啉衍生物的公式(I)及其相关化合物，以及它们作为制备药物组成部分的活性成分的用途。本发明还涉及相关方面，包括制备化合物的过程，含有其中一种或多种化合物的药物组合物，尤其是它们作为神经激素拮抗剂，特别是尿激肽II拮抗剂的用途。
• 4-(Piperidyl-and pyrrolidyl-alkyl-ureido)-quinolines as urotensin II receptor antagonists
  申请人：Aissaoui Hamed

  公开号：US20050043535A1

  公开（公告）日：2005-02-24

  The invention relates to novel 1-pyridin-4-yl urea derivatives and related compounds and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as neurohormonal antagonists.

  本发明涉及新型1-吡啶-4-基脲衍生物及其相关化合物，以及它们作为制备药物组合物的活性成分的用途。本发明还涉及相关方面，包括制备化合物的过程，含有这些化合物中的一个或多个的制药组合物，尤其是它们作为神经荷尔蒙拮抗剂的用途。