methyl (E)-3-amino-2-cyanoprop-2-enoate | 129016-33-7

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 乙烯基酰胺
• 英文名称: methyl (E)-3-amino-2-cyanoprop-2-enoate
• CAS: 129016-33-7
• 化学式: C₅H₆N₂O₂
• 分子量: 126.115
• InChiKey: VAJUIHJBPIKSHM-DUXPYHPUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  9
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  76.1
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl (E)-3-amino-2-cyanoprop-2-enoate 以 甲苯 为溶剂， 反应 24.08h， 生成 2-Propenoic acid, 2-cyano-3-[[(dimethylamino)methylene]amino]-,methyl ester
  参考文献：
  名称：

  Synthesis of conjugated ?-dimethylaminocarbonyl compounds containing an azomethine fragment

  摘要：

  Methods have been studied for synthesis of conjugated omega-dimethylaminocarbonyl compounds containing an azomethine fragment. The structures were established of all products from reaction of 2-aza-3-dimethylaminoacrolein acetal with CH-acids and of DMF acetal and beta-dimethylaminoacrolein aminal with primary amines. It was shown that in many cases these reactions are accompanied by cleavage of the C=N, C-N and C=C bonds.

  DOI：

  10.1007/bf00963505
• 作为产物：
  描述：

  Potassium methyl dicyanoacetate 在 palladium on activated charcoal 氢气 作用下， 以 盐酸 、 甲醇 为溶剂， 生成 methyl (E)-3-amino-2-cyanoprop-2-enoate 、 methyl 3-amino-2-(aminomethyl)propanoate dihydrochloride
  参考文献：
  名称：

  一系列1,3-二氮杂环烷基羧醛肟衍生物的合成及体外毒蕈碱活性。

  摘要：

  合成了一系列的1,3-二氮杂环烷基羧醛肟衍生物，并以[3H]-氧代脱氢吗啡-M（OXO-M）和[3H]-哌仑西平（PZ）作为配体，在受体结合测定中测试了毒蕈碱活性。使用结合研究确定化合物的潜在毒蕈碱激动或拮抗特性，该研究测量了其抑制OXO-M和PZ结合的能力。OXO-M结合的优先抑制被用作潜在的毒蕈碱激动特性的指标；在隔离器官的功能研究中证实了这种潜力。

  DOI：

  10.1016/s0968-0896(01)00379-0

文献信息

• MITTELBACH M.; JUNEK H., Z. NATURFORSCH., 1979, B 34, NO 11, 1580-1586
  作者：MITTELBACH M.、 JUNEK H.

  DOI：——

  日期：——
• Synthesis of conjugated ?-dimethylaminocarbonyl compounds containing an azomethine fragment
  作者：Zh. A. Krasnaya、V. S. Bogdanov

  DOI：10.1007/bf00963505

  日期：1991.10

  Methods have been studied for synthesis of conjugated omega-dimethylaminocarbonyl compounds containing an azomethine fragment. The structures were established of all products from reaction of 2-aza-3-dimethylaminoacrolein acetal with CH-acids and of DMF acetal and beta-dimethylaminoacrolein aminal with primary amines. It was shown that in many cases these reactions are accompanied by cleavage of the C=N, C-N and C=C bonds.
• Synthesis and in vitro muscarinic activities of a Series of 1,3-diazacycloalkyl carboxaldehyde oxime derivatives
  作者：Ralf Plate、Christan G.J.M Jans、Marc J.M Plaum、Thijs de Boer

  DOI：10.1016/s0968-0896(01)00379-0

  日期：2002.4

  tested for muscarinic activity in receptor binding assays using [3H]-oxotremorine-M (OXO-M) and [3H]-pirenzepine (PZ) as ligands. Potential muscarinic agonistic or antagonistic properties of the compounds were determined using binding studies measuring their potencies to inhibit the binding of OXO-M and PZ. Preferential inhibition of OXO-M binding was used as an indicator for potential muscarinic agonistic

  合成了一系列的1,3-二氮杂环烷基羧醛肟衍生物，并以[3H]-氧代脱氢吗啡-M（OXO-M）和[3H]-哌仑西平（PZ）作为配体，在受体结合测定中测试了毒蕈碱活性。使用结合研究确定化合物的潜在毒蕈碱激动或拮抗特性，该研究测量了其抑制OXO-M和PZ结合的能力。OXO-M结合的优先抑制被用作潜在的毒蕈碱激动特性的指标；在隔离器官的功能研究中证实了这种潜力。