tert-butyl N-(3'-hydroxybiphenyl-3-ylmethyl)carbamate | 862541-16-0

• 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: tert-butyl N-(3'-hydroxybiphenyl-3-ylmethyl)carbamate
• 英文别名: tert-butyl [(3'-hydroxybiphenyl-3-yl)methyl]carbamate；tert-butyl N-[[3-(3-hydroxyphenyl)phenyl]methyl]carbamate
• CAS: 862541-16-0
• 化学式: C₁₈H₂₁NO₃
• 分子量: 299.37
• InChiKey: BDMSQLNVFOFUIY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  58.6
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  tert-butyl N-(3'-hydroxybiphenyl-3-ylmethyl)carbamate 、 N-(3-溴丙基)苯二胺 生成 tert-butyl N-[3'-(3-benzyloxycarbonylaminopropoxy)biphenyl-3-ylmethyl]carbamate
  参考文献：
  名称：

  Purinenucleoside derivative modified in 8-position and medical use thereof

  摘要：

  本发明提供了一种8-修饰嘌呤核苷衍生物，该衍生物对于与血浆尿酸水平异常相关的疾病非常有用。式(I)所表示的8-修饰嘌呤核苷衍生物，其前药或其药学上可接受的盐，或其水合物或溶剂化物，对于痛风、高尿酸血症、尿路结石、高尿酸性肾病等的预防或治疗非常有用。在该式中，n为1或2；RA是氢原子或羟基；R1是氢原子、羟基、硫醇基、氨基或氯原子；环J表示可选取的2-萘基团，或由以下通式(II)所表示的团，其中Y表示单键或连接基团；环Z表示可选取的芳基团或杂环芳基团等；R2至R4、P1和Q表示卤素原子、氰基或类似物。

  公开号：

  US20070179115A1
• 作为产物：
  描述：

  3'-(aminomethyl)-[1,1'-biphenyl]-3-ol 、 二碳酸二叔丁酯 在 sodium hydroxide 作用下， 以 1,4-二氧六环 、 水 为溶剂， 以95%的产率得到tert-butyl N-(3'-hydroxybiphenyl-3-ylmethyl)carbamate
  参考文献：
  名称：

  Identification of orally bioavailable, non-amidine inhibitors of Urokinase Plasminogen Activator (uPA)

  摘要：

  In this Letter we report the synthesis and evaluation of a series of non-amidine inhibitors of Urokinase Plasminogen Activator (uPA). Starting from compound 1, a significant change provided compounds in which the amidine, binding in the S1 pocket, was replaced with a primary amine. Further modifications led to the identification of potent, selective, and orally bioavailable uPA inhibitors. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.08.008

文献信息

• Purinenucleoside derivative modified in 8-position and medical use thereof
  申请人：Tatani Kazuya

  公开号：US20070179115A1

  公开（公告）日：2007-08-02

  The present invention provides an 8-modified purinenucleoside derivative which is useful for diseases associated with an abnormality of plasma uric acid level. An 8-modified purinenucleoside derivative represented by the following formula (I), a prodrug thereof or a pharmaceutically acceptable salt thereof, or a hydrate or solvate thereof, is useful for the prevention or treatment of gout, hyperuricemia, urinary lithiasis, hyperuricemic nephropathy or the like. In the formula, n is 1 or 2; R A is a hydrogen atom or a hydroxyl group; R 1 is a hydrogen atom, a hydroxyl group, a thiol group, an amino group or a chlorine atom; ring J represents an optionally substituted 2-naphthyl group, or a group represented by the following general formula (II) wherein Y represents a single bond or a connecting group; ring Z represents an optionally substituted aryl group or heteroaryl group or the like; and R 2 to R 4 , P 1 and Q represents a halogen atom, a cyano group or the like.

  本发明提供了一种用于与血浆尿酸水平异常相关疾病的8-修饰嘌呤核苷衍生物。以下式（I）所代表的一种8-修饰嘌呤核苷衍生物、其前药或药用盐、或其水合物或溶剂化合物，对于痛风、高尿酸血症、尿路结石、高尿酸性肾病等的预防或治疗具有用处。在该式中，n为1或2；RA是氢原子或羟基；R1是氢原子、羟基、硫醇基、氨基或氯原子；环J代表可选地取代的2-萘基，或由以下一般式（II）所代表的基团，其中Y代表单键或连接基团；环Z代表可选地取代的芳基或杂环芳基等；而R2至R4、P1和Q代表卤素原子、氰基或类似物。
• Sulfonamide Derivatives For The Treatment of Diseases
  申请人：Brown Alan Daniel

  公开号：US20080267970A1

  公开（公告）日：2008-10-30

  The invention relates to compounds of formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in numerous diseases, disorders and conditions, in particular inflammatory, allergic and respiratory diseases, disorders and conditions.

  本发明涉及式（1）化合物，以及制备中间体、含有该衍生物的组合物的过程和用途。根据本发明的化合物在许多疾病、疾患和病况中有用，特别是在炎症、过敏和呼吸系统疾病、疾患和病况中有用。
• PURINE NUCLEOSIDE DERIVATIVE MODIFIED IN 8-POSITION AND MEDICAL USE THEREOF
  申请人：Tatani Kazuya

  公开号：US20100249054A9

  公开（公告）日：2010-09-30

  The present invention provides an 8-modified purinenucleoside derivative which is useful for diseases associated with an abnormality of plasma uric acid level. An 8-modified purinenucleoside derivative represented by the following formula (I), a prodrug thereof or a pharmaceutically acceptable salt thereof, or a hydrate or solvate thereof, is useful for the prevention or treatment of gout, hyperuricemia, urinary lithiasis, hyperuricemic nephropathy or the like. In the formula, n is 1 or 2; R A is a hydrogen atom or a hydroxyl group; R 1 is a hydrogen atom, a hydroxyl group, a thiol group, an amino group or a chlorine atom; ring J represents an optionally substituted 2-naphthyl group, or a group represented by the following general formula (II) wherein Y represents a single bond or a connecting group; ring Z represents an optionally substituted aryl group or heteroaryl group or the like; and R 2 to R 4 , P 1 and Q represents a halogen atom, a cyano group or the like.

  本发明提供了一种8-修饰嘌呤核苷衍生物，用于与血浆尿酸水平异常相关的疾病。公式（I）所表示的8-修饰嘌呤核苷衍生物，其前体药物或其药学上可接受的盐，或其水合物或溶剂化物，可用于痛风、高尿酸血症、泌尿系结石、高尿酸性肾病等的预防或治疗。在公式中，n为1或2；RA是氢原子或羟基；R1是氢原子、羟基、硫醇基、氨基或氯原子；环J表示可选取的2-萘基团，或由以下通式（II）所表示的基团，其中Y表示单键或连接基团；环Z表示可选取的芳基团或杂环芳基团等；R2到R4、P1和Q表示卤素原子、氰基或类似物。
• Sulfonamide Derivatives For The Treatment Of Diseases
  申请人：Brown Alan Daniel

  公开号：US20100273758A1

  公开（公告）日：2010-10-28

  The invention relates to compounds of formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in numerous diseases, disorders and conditions, in particular inflammatory, allergic and respiratory diseases, disorders and conditions.

  本发明涉及公式（1）的化合物以及制备这些化合物的中间体、含有这些化合物的组合物和这些衍生物的用途。根据本发明的化合物在许多疾病、紊乱和条件中具有用途，特别是在炎症性、过敏性和呼吸系统疾病、紊乱和条件中。
• Sulfonamide Derivatives for the Treatment of Diseases
  申请人：Brown Alan Daniel

  公开号：US20090197912A1

  公开（公告）日：2009-08-06

  The invention relates to compounds of formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in numerous diseases, disorders and conditions, in particular inflammatory, allergic and respiratory diseases, disorders and conditions.

  本发明涉及公式（1）的化合物，以及用于制备这些衍生物的中间体的制备过程、含有这些化合物的组合物以及这些衍生物的用途。根据本发明的化合物在许多疾病、障碍和病况中有用，特别是在炎症、过敏和呼吸系统疾病、障碍和病况中有用。