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methyl 4H-pyrrolo[2,3-d][1,2,3]thiadiazole-4-carboxylate | 500136-13-0

中文名称
——
中文别名
——
英文名称
methyl 4H-pyrrolo[2,3-d][1,2,3]thiadiazole-4-carboxylate
英文别名
methyl pyrrolo[2,3-d]thiadiazole-4-carboxylate
methyl 4H-pyrrolo[2,3-d][1,2,3]thiadiazole-4-carboxylate化学式
CAS
500136-13-0
化学式
C6H5N3O2S
mdl
——
分子量
183.191
InChiKey
LSLFJEGXOZLMIB-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):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    85.2
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    methyl 4H-pyrrolo[2,3-d][1,2,3]thiadiazole-4-carboxylate甲醇 、 potassium hydroxide 作用下, 反应 16.0h, 以79%的产率得到4H-pyrrolo[2,3-d][1,2,3]thiadiazole
    参考文献:
    名称:
    Investigation of the regioselectivity of the Hurd–Mori reaction for the formation of bicyclic 1,2,3-thiadiazoles
    摘要:
    A series of new pyrrolo[d][1,2,3]thiadiazole carboxylates and 5,6-dihydro-4H-cyclopenta[d][1,2,3]thiadiazoles has been synthesized via the Hurd-Mori reaction. The regioselectivity of the cyclization has been studied and trends were established to predict the cyclization direction to afford bicyclic 1,2,3-thiadiazoles. Effects promoting and disfavoring the reaction have also been investigated to guide the synthesis of scaffolds of this type. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.05.017
  • 作为产物:
    描述:
    methyl 2-[2-(ethoxycarbonyl)hydrazono]pyrrolidine-1-carboxylate 在 氯化亚砜 作用下, 以 二氯甲烷 为溶剂, 以29%的产率得到methyl 4H-pyrrolo[2,3-d][1,2,3]thiadiazole-4-carboxylate
    参考文献:
    名称:
    Investigation of the regioselectivity of the Hurd–Mori reaction for the formation of bicyclic 1,2,3-thiadiazoles
    摘要:
    A series of new pyrrolo[d][1,2,3]thiadiazole carboxylates and 5,6-dihydro-4H-cyclopenta[d][1,2,3]thiadiazoles has been synthesized via the Hurd-Mori reaction. The regioselectivity of the cyclization has been studied and trends were established to predict the cyclization direction to afford bicyclic 1,2,3-thiadiazoles. Effects promoting and disfavoring the reaction have also been investigated to guide the synthesis of scaffolds of this type. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2010.05.017
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文献信息

  • Investigation of the regioselectivity of the Hurd–Mori reaction for the formation of bicyclic 1,2,3-thiadiazoles
    作者:Martin Turner、Thomas Linder、Michael Schnürch、Marko D. Mihovilovic、Peter Stanetty
    DOI:10.1016/j.tet.2010.05.017
    日期:2010.7
    A series of new pyrrolo[d][1,2,3]thiadiazole carboxylates and 5,6-dihydro-4H-cyclopenta[d][1,2,3]thiadiazoles has been synthesized via the Hurd-Mori reaction. The regioselectivity of the cyclization has been studied and trends were established to predict the cyclization direction to afford bicyclic 1,2,3-thiadiazoles. Effects promoting and disfavoring the reaction have also been investigated to guide the synthesis of scaffolds of this type. (C) 2010 Elsevier Ltd. All rights reserved.
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