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8-benzyl-5,6,7,8-tetrahydro-4H-thieno<2,3-b><1,4>diazepine | 213678-66-1

中文名称
——
中文别名
——
英文名称
8-benzyl-5,6,7,8-tetrahydro-4H-thieno<2,3-b><1,4>diazepine
英文别名
8-Benzyl-4,5,6,7-tetrahydrothieno[2,3-b][1,4]diazepine;8-benzyl-4,5,6,7-tetrahydrothieno[2,3-b][1,4]diazepine
8-benzyl-5,6,7,8-tetrahydro-4H-thieno<2,3-b><1,4>diazepine化学式
CAS
213678-66-1
化学式
C14H16N2S
mdl
——
分子量
244.36
InChiKey
XEKGBSXOVXOSGQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    43.5
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    8-benzyl-5,6,7,8-tetrahydro-4H-thieno<2,3-b><1,4>diazepine 在 palladium on activated charcoal 氢气三乙胺 作用下, 以 乙醇二氯甲烷 为溶剂, 25.0 ℃ 、101.33 kPa 条件下, 反应 26.0h, 生成 N-<4-(8-benzyl-5,6,7,8-tetrahydro-4H-thieno<2,3-b><1,4>diazepin-4-yl)carbonyl>phenyl-2-phenylbenzamide
    参考文献:
    名称:
    Synthesis of Novel 5,6,7,8-Tetrahydro-4H-thieno[2,3-b][1,4]diazepine Derivatives
    摘要:
    Unsubstituted 5,6,7, 8-tetrahydro-4H-thieno[2, 3-b][1,4]diazepine (1) and 4H-thieno[2,3-b][1,4]diazepine-5,7(6H,8H)-dione (2) were newly synthesized. Benzoylation of 1 regioselectively afforded thienodiazepine (13) substituted with a benzoyl group nl position 4. Alternatively, novel synthetic procedures were devised to yield thienodiazepine (22) substituted with an alkyl group or compound (14) with an aralkyl group at position 8. Thus, the ingenious introduction of functional groups at the N-4 or 8 position of a thienodiazepine skeleton was achieved and then a variety of 5,6,7,8-tetrahydro-4H-thieno[2,3-b][1,4]diazepines (5)-(9), and (27), some of which exhibited potent arginine vasopressin antagonistic activity, were obtained using the key intermediates and (1), (13), (14) and (22).
    DOI:
    10.3987/com-98-8179
  • 作为产物:
    描述:
    N-benzyl-3-nitrothiophen-2-amine 在 lithium aluminium tetrahydride 、 铁粉溶剂黄146 作用下, 以 四氢呋喃 为溶剂, 反应 51.0h, 生成 8-benzyl-5,6,7,8-tetrahydro-4H-thieno<2,3-b><1,4>diazepine
    参考文献:
    名称:
    Synthesis of Novel 5,6,7,8-Tetrahydro-4H-thieno[2,3-b][1,4]diazepine Derivatives
    摘要:
    Unsubstituted 5,6,7, 8-tetrahydro-4H-thieno[2, 3-b][1,4]diazepine (1) and 4H-thieno[2,3-b][1,4]diazepine-5,7(6H,8H)-dione (2) were newly synthesized. Benzoylation of 1 regioselectively afforded thienodiazepine (13) substituted with a benzoyl group nl position 4. Alternatively, novel synthetic procedures were devised to yield thienodiazepine (22) substituted with an alkyl group or compound (14) with an aralkyl group at position 8. Thus, the ingenious introduction of functional groups at the N-4 or 8 position of a thienodiazepine skeleton was achieved and then a variety of 5,6,7,8-tetrahydro-4H-thieno[2,3-b][1,4]diazepines (5)-(9), and (27), some of which exhibited potent arginine vasopressin antagonistic activity, were obtained using the key intermediates and (1), (13), (14) and (22).
    DOI:
    10.3987/com-98-8179
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文献信息

  • Synthesis of Novel 5,6,7,8-Tetrahydro-4H-thieno[2,3-b][1,4]diazepine Derivatives
    作者:Hidetsura Cho、Kengo Murakami、Akitaka Fujisawa、Misako Niwa、Hiroyuki Nakanishi、Itsuo Uchida
    DOI:10.3987/com-98-8179
    日期:——
    Unsubstituted 5,6,7, 8-tetrahydro-4H-thieno[2, 3-b][1,4]diazepine (1) and 4H-thieno[2,3-b][1,4]diazepine-5,7(6H,8H)-dione (2) were newly synthesized. Benzoylation of 1 regioselectively afforded thienodiazepine (13) substituted with a benzoyl group nl position 4. Alternatively, novel synthetic procedures were devised to yield thienodiazepine (22) substituted with an alkyl group or compound (14) with an aralkyl group at position 8. Thus, the ingenious introduction of functional groups at the N-4 or 8 position of a thienodiazepine skeleton was achieved and then a variety of 5,6,7,8-tetrahydro-4H-thieno[2,3-b][1,4]diazepines (5)-(9), and (27), some of which exhibited potent arginine vasopressin antagonistic activity, were obtained using the key intermediates and (1), (13), (14) and (22).
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同类化合物

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