1-(1-isochromanyl)imidazole | 82746-23-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: 1-(1-isochromanyl)imidazole
• 英文别名: 1-(3,4-dihydro-1H-2-benzopyran-1-yl)-1H-imidazole；Uxrqjtsjgudbpd-uhfffaoysa-；1-(3,4-dihydro-1H-isochromen-1-yl)imidazole
• CAS: 82746-23-4
• 化学式: C₁₂H₁₂N₂O
• 分子量: 200.24
• InChiKey: UXRQJTSJGUDBPD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  27
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  咪唑 、 异色满 在 2-羟基-2-氮杂金刚烷 、 [bis(trifluoroacetoxy)iodo]benzene 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 18.0h， 以90%的产率得到1-(1-isochromanyl)imidazole
  参考文献：
  名称：

  Efficient C(sp³)–H Bond Functionalization of Isochroman by AZADOL Catalysis

  摘要：

  A novel organocatalytic C(sp(3))-H bond functionalization of isochroman under practical conditions has been developed. In the presence of 5.0 mol % of AZADOL, the catalysis proceeded successfully with a broad range of substrates and nucleophiles in excellent yields.

  DOI：

  10.1021/acs.orglett.5b00434

文献信息

• Reactivity of isocoumarins. IV. Reaction of 1-ethoxyisochroman with nucleophilic reagents.
  作者：MASATOSHI YAMATO、TADATAKA ISHIKAWA、SHINJI YAMADA

  DOI：10.1248/cpb.30.843

  日期：——

  As a part of our study on the reactions of 1-ethoxyisochroman (1) with nucleophilic reagents, the reactions of 1 with amines, amides, thioamides, sulfonamides, urea, thiourea, and heterocyclic compounds were examined.

  作为我们对1-乙氧基异香豆素（1）与亲核试剂反应研究的一部分，考察了1与胺、酰胺、硫酰胺、磺酰胺、尿素、硫脲和杂环化合物的反应。
• YAMATO, MASATOSHI;ISHIKAWA, TADATAKA;YAMADA, SHINJI, CHEM. AND PHARM. BULL., 1982, 30, N 3, 843-850
  作者：YAMATO, MASATOSHI、ISHIKAWA, TADATAKA、YAMADA, SHINJI

  DOI：——

  日期：——
• Efficient C(sp³)–H Bond Functionalization of Isochroman by AZADOL Catalysis
  作者：Wataru Muramatsu、Kimihiro Nakano

  DOI：10.1021/acs.orglett.5b00434

  日期：2015.3.20

  A novel organocatalytic C(sp(3))-H bond functionalization of isochroman under practical conditions has been developed. In the presence of 5.0 mol % of AZADOL, the catalysis proceeded successfully with a broad range of substrates and nucleophiles in excellent yields.

表征谱图