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4-amino-3-methyl-5-(N-methylamino)isothiazole | 132026-88-1

中文名称
——
中文别名
——
英文名称
4-amino-3-methyl-5-(N-methylamino)isothiazole
英文别名
4-amino-3-methyl-5-methylaminoisothiazole;5-N,3-dimethyl-1,2-thiazole-4,5-diamine
4-amino-3-methyl-5-(N-methylamino)isothiazole化学式
CAS
132026-88-1
化学式
C5H9N3S
mdl
MFCD19207339
分子量
143.213
InChiKey
OIJGPZRBWYQKSF-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
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    79.2
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    参考文献:
    名称:
    The Synthesis of Substituted Imidazo[4,5-d]isothiazoles via the Ring Annulation of Isothiazole Diamines: An Investigation of the Chemical, Physical, and Biological Properties of Several Novel 5:5 Fused Analogs of the Purine Ring System
    摘要:
    A series of imidazo[4,5-d]isothiazoles have been prepared from isothiazole precursors via a strategy employing ring annulation of the appropriate isothiazole diamine. In this manner, several 4,5-diaminoisothiazoles were converted into the corresponding 5-(alkylthio)imidazo[4,5-d]isothiazoles via a two-step, one-pot procedure in good yield. This methodology proved quite general and allows for the introduction of various substituents onto the 3-, 5-, and 6-positions of this ring system. Reaction with Raney nickel destroyed the ring system, presumably through removal of the sulfur at the 1-position, and the 5-mercapto substituent could not be removed selectively. Ring annulation with diethoxymethyl acetate provided the 5-unsubstituted imidazo[4,5-d]isothiazoles but was less general, and only the 3-methyl derivatives could be prepared. Imidazo[4,5-d]isothiazoles bearing no substituents on nitrogen readily underwent alkylation to afford mixtures of the N-4- and N-6-substituted compounds. The chemical and physical properties of these novel heterocycles were studied in detail, and the structure of 3-methyl-5-methanesulfonyl-6-(phenylmethyl)imidazo[4,5-d] isothiazole was verified by single crystal X-ray diffraction studies.
    DOI:
    10.1021/jo00125a016
  • 作为产物:
    描述:
    3-methyl-5-(N-methylamino)-4-nitroisothiazole 以98%的产率得到4-amino-3-methyl-5-(N-methylamino)isothiazole
    参考文献:
    名称:
    Diazepine antiallergy agents
    摘要:
    公式(I)、(II)或(III)的血小板活化因子拮抗剂:##STR1##其中A是可选择取代的苯、吡啶、萘、喹啉、噻吩、苯并噻吩、吡唑或异噻唑,X是O、S或NH,Y是1,4-苯撑基或公式##STR2##的基团,R.sup.1是H或可选择取代的C.sub.1-C.sub.4烷基,R.sup.2和R.sup.3是H或C.sub.1-C.sub.4烷基,B是可选择融合的含氮的5-或6-成员环,Het是可选择取代的含氮的5-成员杂环环或吡啶环,该环可选择与苯或含氮的杂环环融合。
    公开号:
    US05008263A1
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