methyl 6-aminochromane-2-carboxylate | 847948-85-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: methyl 6-aminochromane-2-carboxylate
• 英文别名: 6-amino-chroman-2-carboxylic acid methyl ester；(R,S)-6-amino-chroman-2-carboxylic acid methyl ester；methyl 6-amino-3,4-dihydro-2H-1-benzopyran-2-carboxylate；methyl 6-amino-3,4-dihydro-2H-chromene-2-carboxylate
• CAS: 847948-85-0
• 化学式: C₁₁H₁₃NO₃
• 分子量: 207.229
• InChiKey: OEJDSGOTKRYTJE-UHFFFAOYSA-N

物化性质

• 沸点：
  363.9±42.0 °C(Predicted)
• 密度：
  1.239±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  61.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl 6-aminochromane-2-carboxylate 在 lithium hydroxide 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 生成 6-(methanesulfonamido)-3,4-dihydro-2H-chromene-2-carboxylic acid
  参考文献：
  名称：

  Potent and highly selective kappa opioid receptor agonists incorporating chroman- and 2,3-dihydrobenzofuran-based constraints

  摘要：

  Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.08.094
• 作为产物：
  描述：

  苯并二氢吡喃-2-羧酸 在 palladium on activated charcoal 盐酸 、 氢气 、 硝酸 作用下， 生成 methyl 6-aminochromane-2-carboxylate
  参考文献：
  名称：

  Potent and highly selective kappa opioid receptor agonists incorporating chroman- and 2,3-dihydrobenzofuran-based constraints

  摘要：

  Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.08.094

文献信息

• Fused bicyclic carboxamide derivatives and methods of their use
  申请人：Dolle E. Roland

  公开号：US20050054630A1

  公开（公告）日：2005-03-10

  Fused bicyclic carboxamide derivatives are disclosed. Pharmaceutical compositions containing the compounds and methods for their use are also disclosed.

  揭示了融合的双环羧酰胺衍生物。还公开了含有这些化合物的药物组合物以及它们的使用方法。
• [EN] HDAC INHIBITORS<br/>[FR] INHIBITEURS DE HDAC
  申请人：UNIV PITTSBURGH COMMONWEALTH SYS HIGHER EDUCATION

  公开号：WO2022120048A1

  公开（公告）日：2022-06-09

  The present disclosure is directed to chromane compounds, chromane compounds demonstrating HDAC inhibition, and pharmaceutical compositions thereof. Additional embodiments include methods of using the chromane compounds. For example, the disclosure includes methods of inhibiting histone acetylation in a cell, comprising contacting the cell with a chromane compound of the disclosure. Additional embodiments include methods of treating a disease capable of treatment by inhibition of histone acetylation in a patient in need thereof, comprising administering a chromane compound of the disclosure.

  本公开涉及色满烷化合物、表现出HDAC抑制作用的色满烷化合物及其制药组合物。其他实施例包括使用色满烷化合物的方法。例如，本公开包括抑制细胞中组蛋白乙酰化的方法，包括将该细胞与本公开中的色满烷化合物接触。其他实施例包括治疗需要抑制组蛋白乙酰化的患者的可治疗疾病的方法，包括给予本公开中的色满烷化合物。
• US7034051B2
  申请人：——

  公开号：US7034051B2

  公开（公告）日：2006-04-25
• [EN] FUSED BICYCLIC CARBOXAMIDE DERIVATIVES AND METHODS OF THEIR USE<br/>[FR] DERIVES DE CARBOXAMIDES BICYCLIQUES FUSIONNES ET LEURS PROCEDES D'UTILISATION
  申请人：ADOLOR CORP

  公开号：WO2005023799A1

  公开（公告）日：2005-03-17

  Fused bicyclic carboxamide derivatives of the general formula (I) are disclosed. Pharmaceutical compositions containing the compounds and methods for their use, inter alia, in treating and/or preventing pain, pruritus, and gastrointestinal disorders are also disclosed.
• Potent and highly selective kappa opioid receptor agonists incorporating chroman- and 2,3-dihydrobenzofuran-based constraints
  作者：Guo-Hua Chu、Minghua Gu、Joel A. Cassel、Serge Belanger、Thomas M. Graczyk、Robert N. DeHaven、Nathalie Conway-James、Mike Koblish、Patrick J. Little、Diane L. DeHaven-Hudkins、Roland E. Dolle

  DOI：10.1016/j.bmcl.2005.08.094

  日期：2005.12

  Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor. (c) 2005 Elsevier Ltd. All rights reserved.