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N-cyclohexylideneisopropanesulfinamide | 1404231-76-0

中文名称
——
中文别名
——
英文名称
N-cyclohexylideneisopropanesulfinamide
英文别名
N-cyclohexylidenepropane-2-sulfinamide
N-cyclohexylideneisopropanesulfinamide化学式
CAS
1404231-76-0
化学式
C9H17NOS
mdl
——
分子量
187.306
InChiKey
GADNZICILBXWCT-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):
    1.4
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    48.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    苯硼酸酐N-cyclohexylideneisopropanesulfinamide 在 chloro(1,5-cyclooctadiene)rhodium(I) dimer 、 1,2-diphenylphosphinobenzenesodium ethanolate 作用下, 以 1,4-二氧六环乙醇 为溶剂, 以67%的产率得到N-(1-phenylcyclohexyl)isopropanesulfinylamine
    参考文献:
    名称:
    Rh-Catalyzed Addition of Arylboroxines to Cyclic N-(Isopropanesulfinyl)ketimines
    摘要:
    Arylboroxines, which are easily accessed by drying commercially available arylboronic acids, are added to N-(isopropanesulfinyl)ketimines derived from cyclohexanone, N-Boc-piperidin-4-one, and tetrahydropyran-4-one in high yields and with excellent functional group compatibility via rhodium catalysis. These results contrast with additions to the corresponding ketimines incorporating the larger N-tert-butanesulfinyl group, which give considerably lower yields. Efficient two-step preparation of racemic isopropanesulfinamide from inexpensive isopropyl disulfide and recycling of the isopropanesulfinyl group from the addition products are also described.
    DOI:
    10.1021/jo301634y
  • 作为产物:
    描述:
    propane-2-sulfinamide环己酮titanium(IV) isopropylate 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 以56%的产率得到N-cyclohexylideneisopropanesulfinamide
    参考文献:
    名称:
    Rh-Catalyzed Addition of Arylboroxines to Cyclic N-(Isopropanesulfinyl)ketimines
    摘要:
    Arylboroxines, which are easily accessed by drying commercially available arylboronic acids, are added to N-(isopropanesulfinyl)ketimines derived from cyclohexanone, N-Boc-piperidin-4-one, and tetrahydropyran-4-one in high yields and with excellent functional group compatibility via rhodium catalysis. These results contrast with additions to the corresponding ketimines incorporating the larger N-tert-butanesulfinyl group, which give considerably lower yields. Efficient two-step preparation of racemic isopropanesulfinamide from inexpensive isopropyl disulfide and recycling of the isopropanesulfinyl group from the addition products are also described.
    DOI:
    10.1021/jo301634y
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文献信息

  • NPYY5 antagonists
    申请人:Shionogi&Co., Ltd.
    公开号:EP2014285A1
    公开(公告)日:2009-01-14
    The present invention provides a pharmaceutical composition for use as an NPY Y5 receptor antagonist comprising a compound of the formula (I): wherein R1 is lower alkyl, cycloalkyl or the like, R2 is hydrogen, lower alkyl or the like, n is 1 or 2, X is lower alkylene, lower alkenylene, arylene, cycloalkylene or the like, Y is CONR7, CSNR7, NR7CO, NR7CS or the like, Z is lower alkyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl or the like and R7 is hydrogen or lower alkyl, prodrug, pharmaceutically acceptable salt or solvate thereof
    本发明提供了一种用作 NPY Y5 受体拮抗剂的药物组合物,该组合物由式(I)化合物组成: 其中 R1 是低级烷基、环烷基或类似物、 R2 是氢、低级烷基或类似物、 n 是 1 或 2、 X 是低级烯烃、低级烯烃、芳基、环烷烃或类似物、 Y 是 CONR7、CSNR7、NR7CO、NR7CS 或类似物、 Z 是低级烷基、任选取代的碳环烷基、任选取代的杂环烷基或类似物,R7 是氢或低级烷基、 其原药、药学上可接受的盐或溶液
  • Rh-Catalyzed Addition of Arylboroxines to Cyclic <i>N</i>-(Isopropanesulfinyl)ketimines
    作者:Hyung Hoon Jung、Andrew W. Buesking、Jonathan A. Ellman
    DOI:10.1021/jo301634y
    日期:2012.11.2
    Arylboroxines, which are easily accessed by drying commercially available arylboronic acids, are added to N-(isopropanesulfinyl)ketimines derived from cyclohexanone, N-Boc-piperidin-4-one, and tetrahydropyran-4-one in high yields and with excellent functional group compatibility via rhodium catalysis. These results contrast with additions to the corresponding ketimines incorporating the larger N-tert-butanesulfinyl group, which give considerably lower yields. Efficient two-step preparation of racemic isopropanesulfinamide from inexpensive isopropyl disulfide and recycling of the isopropanesulfinyl group from the addition products are also described.
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