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8-methoxy-5-phenyl-2,3-dihydro-1,4-benzothiazepine | 1443148-13-7

中文名称
——
中文别名
——
英文名称
8-methoxy-5-phenyl-2,3-dihydro-1,4-benzothiazepine
英文别名
——
8-methoxy-5-phenyl-2,3-dihydro-1,4-benzothiazepine化学式
CAS
1443148-13-7
化学式
C16H15NOS
mdl
——
分子量
269.367
InChiKey
HCYMWVKSGIZTPQ-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):
    3.5
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    46.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    8-methoxy-5-phenyl-2,3-dihydro-1,4-benzothiazepine 在 sodium tetrahydroborate 作用下, 以 甲醇乙醇丙酮 为溶剂, 反应 3.0h, 生成
    参考文献:
    名称:
    Transformations of tetrahydro-1,4-benzoxazepines and tetrahydro-1,4-benzothiazepines under the action of alkynes. First example of the synthesis of tetrahydro-1,4-benzothiazonine-6-carboxylate
    摘要:
    It was shown that 2,3,4,5-tetrahydro-1,4-benzoxazepines were cleaved at the N-C(5) bond under the action of activated alkynes in methanol, forming o-(methoxyethyl)- and o-(methoxybenzyl)-phenyl(aminoethyl) ethers. The cleavage rate depended on the electronic effects of the substituents at the C-5 atom. Thiazepine ring expansion in tetrahydro-1,4-benzothiazepine was achieved for the first time via reaction with methyl propiolate to give a benzothiazonine.
    DOI:
    10.1007/s10593-013-1251-z
  • 作为产物:
    参考文献:
    名称:
    Transformations of tetrahydro-1,4-benzoxazepines and tetrahydro-1,4-benzothiazepines under the action of alkynes. First example of the synthesis of tetrahydro-1,4-benzothiazonine-6-carboxylate
    摘要:
    It was shown that 2,3,4,5-tetrahydro-1,4-benzoxazepines were cleaved at the N-C(5) bond under the action of activated alkynes in methanol, forming o-(methoxyethyl)- and o-(methoxybenzyl)-phenyl(aminoethyl) ethers. The cleavage rate depended on the electronic effects of the substituents at the C-5 atom. Thiazepine ring expansion in tetrahydro-1,4-benzothiazepine was achieved for the first time via reaction with methyl propiolate to give a benzothiazonine.
    DOI:
    10.1007/s10593-013-1251-z
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