6-Tert-butylpyrazin-2-amine | 1159821-02-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 6-Tert-butylpyrazin-2-amine
• CAS: 1159821-02-9
• 化学式: C₈H₁₃N₃
• 分子量: 151.21
• InChiKey: WEUGLTGCODMQBB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  51.8
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• PYRIDINE AND PYRAZINE COMPOUNDS AS INHIBITORS OF RIPK2
  申请人：Boehringer Ingelheim International GmbH

  公开号：US20180072703A1

  公开（公告）日：2018-03-15

  The present invention relates to compounds of formula (I): or pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , X, Y, and HET are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes

  本发明涉及以下式（I）的化合物： 或其药用可接受的盐，其中R 1 ，R 2 ，X，Y和HET如本文所定义。该发明还涉及包含这些化合物的药物组合物，使用这些化合物治疗各种疾病和紊乱的方法，制备这些化合物的方法以及在这些过程中有用的中间体。
• Antibacterial Compositions
  申请人：Haydon David John

  公开号：US20110263590A1

  公开（公告）日：2011-10-27

  Compounds of formula (I) have antibacterial activity: wherein: m is 0 or 1; Q is hydrogen or cyclopropyl; Alk is an optionally substituted, divalent C 1 -C 6 alkylene, alkenylene or alkynylene radical which may contain an ether (—O—), thioether (—S—) or amino (—NR)— link, wherein R is hydrogen, —CN or C 1 -C 3 alkyl; X is —C(═O)NR 6 —, —S(O)NR 6 —, —C(═O)O— or —S(═O)O— wherein R 6 is hydrogen, optionally substituted C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, -Cyc, or —(C 1 -C 3 alkyl)-Cyc wherein Cyc is optionally substituted monocyclic carbocyclic or heterocyclic having 3-7 ring atoms; Z is N or CH, or CF; R 2 and R 3 are as defined in the description.

  式(I)的化合物具有抗菌活性：其中：m为0或1；Q为氢或环丙基；Alk为可选取代的二价C1-C6烷基、烯基或炔基基团，其中可以含有醚（—O—）、硫醚（—S—）或氨基（—NR）键，其中R为氢、—CN或C1-C3烷基；X为—C（═O）NR6—、—S（O）NR6—、—C（═O）O—或—S（═O）O—，其中R6为氢、可选取代的C1-C6烷基、C2-C6烯基、C2-C6炔基、-Cyc或—（C1-C3烷基）-Cyc，其中Cyc为可选取代的具有3-7个环原子的单环碳环或杂环；Z为N或CH，或CF；R2和R3如描述中所定义。
• Acetylenic Heteroaryl Compounds
  申请人：Wang Yihan

  公开号：US20130018046A1

  公开（公告）日：2013-01-17

  This invention relates to compounds of the general formula: in which the variable groups are as defined herein, and to their preparation and use.

  本发明涉及通式如下的化合物：其中变量基团如本文所定义，以及它们的制备和使用。
• ANTIBACTERIAL CONDENSED THIAZOLES
  申请人：Haydon David John

  公开号：US20100305067A1

  公开（公告）日：2010-12-02

  Compound of formula (I) have antibacterial activity: wherein: m is 0 or 1; Q is hydrogen or cyclopropyl; AIk is an optionally substituted, divalent C 1 -C 6 alkylene, alkenylene or alkynylene radical which may contain an ether (—O—), thioether (—S—) or amino (—NR)— link, wherein R is hydrogen, —CN or C 1 -C 3 alkyl; X is —C(═O)NR 6 —, or —C(═O)O— wherein R 6 is hydrogen, optionally substituted C 1 -C 6 alkyl, C 2 -C 6 alkenyl or C 2 -C 6 alkynyl; Z 1 is —N═ or —CH═Z 2 is —N═ or —C(R 1 )═; R 1 is hydrogen, methyl, ethyl, ethenyl, ethynyl, methoxy, mercapto, mercaptomethyl, halo, fully or partially fluorinated (C 1 -C 2 )alkyl, (C 1 -C 2 Jalkoxy or (C 1 -C 2 )alkylthio, nitro, or nitrile (—CN); R 2 is a group Q 1 -[Alk 1 ]q-Q 2 -, wherein q is 0 or 1; AIk1 is an optionally substituted, divalent, straight chain or branched C 1 -C 6 alkylene, or C 2 -C 6 alkenylene or C 2 -C 6 alkynylene radical which may contain or terminate in an ether (—O—), thioether (—S—) or amino (—NR)— link; Q 2 is an optionally substituted divalent monocyclic carbocyclic or heterocyclic radical having 5 or 6 ring atoms or an optionally substituted divalent bicyclic carbocyclic or heterocyclic radical having 9 or 10 ring atoms; Q 1 is hydrogen, an optional substituent, or an optionally substituted carbocyclic or heterocyclic radical having 3-7 ring atoms.

  式(I)的化合物具有抗菌活性：其中：m为0或1；Q为氢或环丙基；AIk为可选取代的二价C1-C6烷基、烯基或炔基，其中可以含有醚（—O—）、硫醚（—S—）或氨基（—NR）连接，其中R为氢、—CN或C1-C3烷基；X为—C（═O）NR6—或—C（═O）O—，其中R6为氢、可选取代的C1-C6烷基、C2-C6烯基或C2-C6炔基；Z1为—N═或—CH═，Z2为—N═或—C（R1）═；R1为氢、甲基、乙基、乙烯基、乙炔基、甲氧基、巯基、巯基甲基、卤素、全氟或部分氟化的（C1-C2）烷基、（C1-C2）烷氧基或（C1-C2）烷硫基、硝基或腈（—CN）；R2为Q1-[Alk1]q-Q2-基团，其中q为0或1；AIk1为可选取代的二价直链或支链C1-C6烷基、C2-C6烯基或C2-C6炔基，其中可以含有或以醚（—O—）、硫醚（—S—）或氨基（—NR）连接结束；Q2为可选取代的具有5或6个环原子的单环碳环或杂环基团或可选取代的具有9或10个环原子的双环碳环或杂环基团；Q1为氢、可选取代的取代基或具有3-7个环原子的可选取代的碳环或杂环基团。
• ANTIBACTERIAL COMPOSITIONS
  申请人：Haydon David John

  公开号：US20100311766A1

  公开（公告）日：2010-12-09

  Compounds of formula (I) have antibacterial activity wherein: m is O or 1; Q is hydrogen or cyclopropyl; AIk is an optionally substituted, divalent C 1 -C 3 alkylene, C 2 -C 3 alkenylene or C 2 -C 3 alkynylene radical; X is —C(═O)NH— or —C(═O)O—; R 2 and R 3 are as defined in the specification.

  化合物的公式(I)具有抗菌活性，其中：m为O或1; Q为氢或环丙基; AIk为可选取代的二价C1-C3烷基，C2-C3烯基或C2-C3炔基基团; X为—C(═O)NH—或—C(═O)O—; R2和R3如规范中所定义。