3-Butyl-3-ethyl-2,3-dihydrobenzothiepine | 178678-37-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 硫色烯
• 英文名称: 3-Butyl-3-ethyl-2,3-dihydrobenzothiepine
• 英文别名: 3-butyl-3-ethyl-2H-1-benzothiepine
• CAS: 178678-37-0
• 化学式: C₁₆H₂₂S
• 分子量: 246.417
• InChiKey: ZTWKMAVJNRKHNH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  25.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  3-Butyl-3-ethyl-2,3-dihydrobenzothiepine 在 sodium hydroxide 、 间氯过氧苯甲酸 、 sodium sulfite 作用下， 以 CHCl 、 二氯甲烷 为溶剂， 以0.08 g (17%)的产率得到(1aα,2α,8bα) 2-Butyl-2-ethyl-1a,2,3,8b-tetrahydro-benzothiepino[4,5-b]oxirene-4,4-dioxide
  参考文献：
  名称：

  Novel benzothiepines having activity as inhibitors of lleal bile acid transport and taurocholate uptake

  摘要：

  提供了新型苯硫杂吲哚类化合物及其衍生物和类似物；含有它们的药物组合物；以及在医学中使用这些化合物和组合物的方法，特别是在哺乳动物中预防和治疗高脂血症状，如与动脉粥样硬化或高胆固醇血症相关的情况。

  公开号：

  US20040014803A1
• 作为产物：
  描述：

  2-Ethyl-2-((2-formylphenyl)thiomethyl)hexenal 在 TiCl₃ 锌 作用下， 以 乙二醇二甲醚 、 二氯甲烷 为溶剂， 以0.41 g (20%)的产率得到3-Butyl-3-ethyl-2,3-dihydrobenzothiepine
  参考文献：
  名称：

  Novel benzothiepines having activity as inhibitors of lleal bile acid transport and taurocholate uptake

  摘要：

  提供了新型苯硫杂吲哚类化合物及其衍生物和类似物；含有它们的药物组合物；以及在医学中使用这些化合物和组合物的方法，特别是在哺乳动物中预防和治疗高脂血症状，如与动脉粥样硬化或高胆固醇血症相关的情况。

  公开号：

  US20040014803A1

文献信息

• Novel benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake
  申请人：G.D. Searle & Co.

  公开号：US20020013476A1

  公开（公告）日：2002-01-31

  Provided are novel benzothiepines, derivatives, and analogs thereof; pharmaceutical compositions containing them; and methods of using these compounds and compositions in medicine, particularly in the prophylaxis and treatment of hyperlipidemic conditions such as those associated with atherosclerosis or hypercholesterolemia, in mammals.

  提供了新型苯并噻吩类化合物及其衍生物和类似物；含有它们的药物组合物；以及在医学中使用这些化合物和组合物的方法，特别是在哺乳动物中预防和治疗高脂血症状，如与动脉粥样硬化或高胆固醇血症相关的情况。
• Substituted 5-aryl-benzothiepines having activity as inhibitors of ileal
  申请人：G.D. Searle and Company

  公开号：US06107494A1

  公开（公告）日：2000-08-22

  Provided are novel benzothiepines, derivatives, and analogs thereof; pharmaceutical compositions containing them; and methods of using these compounds and compositions in medicine, particularly in the prophylaxis and treatment of hyperlipidemic conditions such as those associated with atherosclerosis or hypercholesterolemia, in mammals.

  提供了新型苯硫杂吲哚类化合物及其衍生物和类似物；包含它们的药物组合物；以及在医学中使用这些化合物和组合物的方法，特别是在哺乳动物中预防和治疗高脂血症状，如与动脉粥样硬化或高胆固醇血症相关的情况。
• Benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake
  申请人：G.D. Searle & Co.

  公开号：US06387924B2

  公开（公告）日：2002-05-14

  Provided are novel benzothiepines, derivatives, and analogs thereof; pharmaceutical compositions containing them; and methods of using these compounds and compositions in medicine, particularly in the prophylaxis and treatment of hyperlipidemic conditions such as those associated with atherosclerosis or hypercholesterolemia, in mammals.

  提供了新颖的苯硫杂环丙烷类化合物及其衍生物和类似物；含有它们的药物组合物；以及在医学中使用这些化合物和组合物的方法，特别是在哺乳动物中预防和治疗与动脉粥样硬化或高胆固醇血症相关的高脂血症条件。
• Combination therapy employing ileal bile acid transport inhibiting benzothiepines and HMG Co-A reductase inhibitors
  申请人：G. D. Searle & Co.

  公开号：US06268392B1

  公开（公告）日：2001-07-31

  Provided are novel benzothiepines, derivatives, and analogs thereof; pharmaceutical compositions containing them; and methods of using these compounds and compositions in medicine, particularly in the prophylaxis and treatment of hyperlipidemic conditions such as those associated with atherosclerosis or hypercholesterolemia, in mammals. Also provided are compositions and methods for combination therapy employing ileal bile acid transport inhibitors and EG Co-A reductase inhibitors for the treatment of hyperlipidemic conditions.

  提供了新型苯硫氮杂环化合物，其衍生物和类似物；含有它们的药物组合物；以及在医学中使用这些化合物和组合物的方法，特别是在哺乳动物中用于预防和治疗高脂血症状，如与动脉粥样硬化或高胆固醇血症相关的情况。还提供了使用回肠胆酸转运抑制剂和EG Co-A还原酶抑制剂联合治疗高脂血症状的组合疗法的组合物和方法。
• Novel mono- and di-fluorinated benzothiepine compouds as inhibitors of apical sodium co-dependent bile acid transport (ASBT) and taurocholate uptake
  申请人：G.D. SEARLE, LLC

  公开号：US20040067872A1

  公开（公告）日：2004-04-08

  Mono-fluorinated and di-fluorinated benzothiepine apical sodium co-dependent bile acid transport (ASBT) inhibitors are disclosed together with methods of making the same, methods of using the same to treat hyperlipidemic conditions as well as pharmaceutical compositions containing the same compounds.

  本发明公开了单氟和二氟苯并噻吩顶部钠依赖性胆酸转运体（ASBT）抑制剂，以及制备这些抑制剂的方法，使用这些抑制剂治疗高脂血症的方法，以及含有这些化合物的药物组合物。