2,3-dihydro-2-(4'-methylphenyl)-4-phenyl-1,5-benzothiazepine | 60246-75-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并硫氮卓类
• 英文名称: 2,3-dihydro-2-(4'-methylphenyl)-4-phenyl-1,5-benzothiazepine
• 英文别名: 4-phenyl-2-p-tolyl-2,3-dihydro-benzo[b][1,4]thiazepine；2-(4-Methylphenyl)-4-phenyl-2,3-dihydro-1,5-benzothiazepine
• CAS: 60246-75-5
• 化学式: C₂₂H₁₉NS
• 分子量: 329.466
• InChiKey: BDUFIUKJOJCAHE-UHFFFAOYSA-N

物化性质

• 熔点：
  148 °C(Solv: ethanol (64-17-5); water (7732-18-5))
• 沸点：
  483.4±45.0 °C(Predicted)
• 密度：
  1.13±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  24
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  37.7
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2,3-dihydro-2-(4'-methylphenyl)-4-phenyl-1,5-benzothiazepine 、 phenylhydroxamoyl chloride 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以50%的产率得到3a,4-dihydro-1,3a-diphenyl-5-(4-methylphenyl)-5H-<1,2,4>oxadiazolo<5,4-d><1,5>benzothiazepine
  参考文献：
  名称：

  5H-[1,2,4]Oxadiazolo[5,4-d][1,5]benzothiazepines as anticonvulsant agents in DBA/2 mice

  摘要：

  A series of 3a,4-dihydro-5H-[1,2,4]oxadiazolo[5,4-d] [1,5]benzothiazepines have been synthesized by 1,3-dipolar cycloaddition reaction of benzonitriloxide to the C=N double bond of 1,5-benzothiazepine derivatives, and the stereochemical features of compounds obtained have been determined by NMR spectroscopy. The results of evaluation of their activity in preventing seizures induced by audiogenic stimulation in DBA/2 mice are also reported and discussed. The 5-(4-bromophenyl)1,3-diphenyl derivative 3b, the most active compound of the series, is over 20 times more active than the parent benzothiazepine Ib and shows an activity comparable to clobazam and better than desmethylclobazam.

  DOI：

  10.1016/0223-5234(96)88311-5
• 作为产物：
  描述：

  3-(2-aminophenylthio)-1-phenyl-3-p-tolylpropan-1-one 以84%的产率得到
  参考文献：
  名称：

  LEVAI A.; BOGNAR R., ACTA CHIM. ACAD. SCI. HUNG. , 1976, 88, NO 3, 293-300

  摘要：

  DOI：

文献信息

• Chen; Zhong; Zhang, Journal of Chemical Research - Part S, 2000, # 8, p. 386 - 387
  作者：Chen、Zhong、Zhang

  DOI：——

  日期：——
• In silico studies on 2,3-dihydro-1,5-benzothiazepines as cholinesterase inhibitors
  作者：Farzana Latif Ansari、Saima Kalsoom、Zaheer-ul-Haq、Zahra Ali、Farukh Jabeen

  DOI：10.1007/s00044-011-9754-6

  日期：2012.9

  In vitro studies on cholinesterase inhibitory potential on the three sets of 2,3-dihydro-1,5-benzothiazepines have been carried out. The compounds in Set 1 were unsubstituted on ring A, while those in Sets 2 and 3 had a 2'- and 3'-hydoxy substituent, respectively, in ring A. These studies revealed that they are mixed inhibitors of both AChE and BChE as reflected from their IC50 values. It was further observed that 3'-hydroxy substituted benzothiazepines (Set 3) were found to have stronger affinity for both AChE and BChE compared with those of Sets 1 and 2. Moreover, all the compounds in Set 3 were found to be stronger BChE inhibitors than AChE. These experimental observations were rationalized by conducting in silico studies using molecular docking tool of Molecular Operating Environment (MOE) software, thereby, a good correlation was observed between IC50 values and their binding interactions within the enzyme active site. We have observed that these interactions were electrostatic and hydrophobic in nature besides hydrogen bonding. The high BChE inhibitory potential of 3'-hydroxy substituted benzothiazepines was found to be cumulative effect of hydrogen bonding and pi-pi interactions between the ligand and BChE. These findings may serve as a guideline for synthesizing more potent ChE inhibitors for the treatment of Alzheimer's disease and related dementias.
• Solunke, Anil B.; More, Mahesh P.; Agare, Sandip U., Indian Journal of Heterocyclic Chemistry, 2022, vol. 32, # 4, p. 479 - 485
  作者：Solunke, Anil B.、More, Mahesh P.、Agare, Sandip U.、Pardeshi, Sandeep D.、Sonar, Jayant P.、Kadre, Tanuja V.

  DOI：——

  日期：——
• 5H-[1,2,4]Oxadiazolo[5,4-d][1,5]benzothiazepines as anticonvulsant agents in DBA/2 mice
  作者：G De Sarro、A Chimirri、A De Sarro、R Gitto、S Grasso、M Zappalà

  DOI：10.1016/0223-5234(96)88311-5

  日期：1995.1

  A series of 3a,4-dihydro-5H-[1,2,4]oxadiazolo[5,4-d] [1,5]benzothiazepines have been synthesized by 1,3-dipolar cycloaddition reaction of benzonitriloxide to the C=N double bond of 1,5-benzothiazepine derivatives, and the stereochemical features of compounds obtained have been determined by NMR spectroscopy. The results of evaluation of their activity in preventing seizures induced by audiogenic stimulation in DBA/2 mice are also reported and discussed. The 5-(4-bromophenyl)1,3-diphenyl derivative 3b, the most active compound of the series, is over 20 times more active than the parent benzothiazepine Ib and shows an activity comparable to clobazam and better than desmethylclobazam.
• LEVAI A.; BOGNAR R., ACTA CHIM. ACAD. SCI. HUNG. <ACAS-A2>, 1976, 88, NO 3, 293-300
  作者：LEVAI A.、 BOGNAR R.

  DOI：——

  日期：——