ethyl 8-chloro-4H-thieno[3,2-c]chromene-2-carboxylate | 634157-18-9

• 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: ethyl 8-chloro-4H-thieno[3,2-c]chromene-2-carboxylate
• CAS: 634157-18-9
• 化学式: C₁₄H₁₁ClO₃S
• 分子量: 294.759
• InChiKey: FNQXLENRBVBPQR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  63.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  ethyl 8-chloro-4H-thieno[3,2-c]chromene-2-carboxylate 在 sodium hydroxide 作用下， 以 四氢呋喃 、 水 为溶剂， 生成 8-chloro-4H-thieno[3,2-c]chromene-2-carboxylic acid
  参考文献：
  名称：

  4H-Thieno[3,2-c]chromene based inhibitors of Notum Pectinacetylesterase

  摘要：

  A group of small molecule thienochromenes inhibitors of Notum Pectinacetylesterase are described. We developed SAR on three series based on carbon, oxygen and sulfur replacement of the 5-position. In each series, highly potent Notum Pectinacetylesterase inhibitors were identified. (C) 2016 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2016.01.038
• 作为产物：
  描述：

  6-氯-4-二氢色原酮 在 sodium ethanolate 、 三氯氧磷 作用下， 生成 ethyl 8-chloro-4H-thieno[3,2-c]chromene-2-carboxylate
  参考文献：
  名称：

  4H-Thieno[3,2-c]chromene based inhibitors of Notum Pectinacetylesterase

  摘要：

  A group of small molecule thienochromenes inhibitors of Notum Pectinacetylesterase are described. We developed SAR on three series based on carbon, oxygen and sulfur replacement of the 5-position. In each series, highly potent Notum Pectinacetylesterase inhibitors were identified. (C) 2016 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2016.01.038

文献信息

• 4H-Thieno[3,2-c]chromene based inhibitors of Notum Pectinacetylesterase
  作者：Qiang Han、Praveen K. Pabba、Joseph Barbosa、Ross Mabon、Jason P. Healy、Michael W. Gardyan、Kristen M. Terranova、Robert Brommage、Andrea Y. Thompson、James M. Schmidt、Alan G.E. Wilson、Xiaolian Xu、James E. Tarver、Kenneth G. Carson

  DOI：10.1016/j.bmcl.2016.01.038

  日期：2016.2

  A group of small molecule thienochromenes inhibitors of Notum Pectinacetylesterase are described. We developed SAR on three series based on carbon, oxygen and sulfur replacement of the 5-position. In each series, highly potent Notum Pectinacetylesterase inhibitors were identified. (C) 2016 Elsevier Ltd. All rights reserved.