3-methyl-2-oxobenzoxazolin-6-ylsulfonic acid | 1216666-32-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶唑类
• 英文名称: 3-methyl-2-oxobenzoxazolin-6-ylsulfonic acid
• 英文别名: 3-Methyl-2-oxobenzoxazolin-6-ylsulfonic acid；3-methyl-2-oxo-1,3-benzoxazole-6-sulfonic acid
• CAS: 1216666-32-8
• 化学式: C₈H₇NO₅S
• 分子量: 229.213
• InChiKey: WJAAPAVEGATBRV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.1
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  92.3
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-methyl-2-oxobenzoxazolin-6-ylsulfonic acid 在 氯磺酸 、 三乙胺 作用下， 以 丙酮 为溶剂， 反应 3.0h， 生成 3-methyl-2-oxobenzoxazoline-6-sulfonic acid diethylamide
  参考文献：
  名称：

  Benzazoles. 4. Synthesis and chemical reactions of 6-chlorosulfonylbenzoxazolin-2-ones

  摘要：

  The corresponding 6-chlorosulfonyl derivatives were synthesized from benzoxazolin-2-one and its 3-methyl derivative by treatment with chlorosulfonic acid. By treatment of the compounds obtained with water and other nucleophilic reagents (aliphatic and heterocyclic amines) 2-oxobenzoxazoline-6-sulfonic acids and a series of their amides were obtained, while reduction with SnCl2 center dot 2H(2)O gave 6-mercaptobenzoxazolin-2-ones.

  DOI：

  10.1007/s10593-011-0724-1
• 作为产物：
  描述：

  3-甲基-2-氧代-2,3-二氢-1,3-苯并唑-6-磺酰氯 在 水 作用下， 反应 2.0h， 以87%的产率得到3-methyl-2-oxobenzoxazolin-6-ylsulfonic acid
  参考文献：
  名称：

  Benzazoles. 4. Synthesis and chemical reactions of 6-chlorosulfonylbenzoxazolin-2-ones

  摘要：

  The corresponding 6-chlorosulfonyl derivatives were synthesized from benzoxazolin-2-one and its 3-methyl derivative by treatment with chlorosulfonic acid. By treatment of the compounds obtained with water and other nucleophilic reagents (aliphatic and heterocyclic amines) 2-oxobenzoxazoline-6-sulfonic acids and a series of their amides were obtained, while reduction with SnCl2 center dot 2H(2)O gave 6-mercaptobenzoxazolin-2-ones.

  DOI：

  10.1007/s10593-011-0724-1

文献信息

• [EN] SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS<br/>[FR] PYRIMIDINYL-AMINES SUBSTITUÉES EN TANT QU'INHIBITEURS DE LA PROTÉINE KINASE
  申请人：SCRIPPS RESEARCH INST

  公开号：WO2009032861A1

  公开（公告）日：2009-03-12

  The present invention provides novel substituted pyrimidinyl-amines that are useful as inhibitors of protein kinases, especially c-Jun N-terminal kinases (JNK) and pharmaceutical compositions thereof and methods of using the same for treating conditions responsive to the inhibition of the JNK pathway.

  本发明提供了一种新型的取代嘧啶基胺，可用作蛋白激酶抑制剂，特别是c-Jun N-末端激酶（JNK）的抑制剂，以及包含它们的药物组合物和使用相同的方法来治疗对JNK途径抑制敏感的疾病。
• SUBSTITUTED TETRAHYDROISOQUINOLINE COMPOUND, THEIR PREPARATION AND USE IN MEDICAMENTS
  申请人：Mas Prio Josep

  公开号：US20090209528A1

  公开（公告）日：2009-08-20

  The present invention relates to substituted tetrahydroisoquinoline compounds of general formula (I), a process for their preparation, medicaments comprising said substituted tetrahydroisoquinoline compounds as well as the use of said substituted tetrahydroisoquinoline compounds for the preparation of medicaments, which are particularly suitable for the prophylaxis and/or treatment of disorders or diseases that are at least partially mediated via 5-HT 6 receptors.

  本发明涉及一般式(I)的取代四氢异喹啉化合物，其制备方法，包含所述取代四氢异喹啉化合物的药物以及利用所述取代四氢异喹啉化合物制备药物，特别适用于预防和/或治疗至少部分通过5-HT6受体介导的疾病或疾病的用途。
• SUBSTITUTED TETRAHYDROISOQUINOLINE COMPOUNDS, THEIR PREPARATION AND USE IN MEDICAMENTS
  申请人：LABORATORIOS DEL DR. ESTEVE, S.A.

  公开号：EP2007729B1

  公开（公告）日：2012-06-27
• SULFONAMIDE SUBSTITUTED PYRAZOLINE COMPOUNDS, THEIR PREPARATION AND USE AS CB1 MODULATORS
  申请人：Laboratorios Del. Dr. Esteve, S.A.

  公开号：EP2079701A1

  公开（公告）日：2009-07-22
• SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS
  申请人：The Scripps Research Institute

  公开号：EP2200436A1

  公开（公告）日：2010-06-30