2-carbamoylaziridine | 5950-35-6

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 2-carbamoylaziridine
• 英文别名: aziridine-2-carboxamide；leakadine；Aziridin-2-carbonsaeureamid；2-aziridine-carboxamide；2-Aziridinecarboxamide
• CAS: 5950-35-6
• 化学式: C₃H₆N₂O
• 分子量: 86.0934
• InChiKey: LZRVAAYXGFWSDY-UHFFFAOYSA-N

物化性质

• 熔点：
  116-118 °C
• 沸点：
  309.7±31.0 °C(Predicted)
• 密度：
  1.271±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -1.5
• 重原子数：
  6
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  65
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-carbamoylaziridine 以 neat liquid 为溶剂， 以97%的产率得到1-(2,3-diamino-3-oxopropyl)aziridine-2-carboxamide
  参考文献：
  名称：

  2-Carbamoylaziridine (Leakadine): diastereoselective transformations and stereoelectronic effect*

  摘要：

  Diastereoselective transformations of Leakadine were discovered: dimerization during melting or heating in CHCl3 with the formation of one diastereomer. The obtained dimer reacts with methyl isocyanate under mild conditions with the formation of an N-methylcarbamoyl derivative - also in the form of one diastereomer. In the diastereoselective reaction of Leakadine with dimethyl formamide dimethyl acetal, 2-dimethylamino-1,3-diazabicyclo[3.1.0]hexan-4-one was obtained. The reaction of Leakadine with perfluoroisobutylene was studied.

  DOI：

  10.1007/s10593-012-1068-1
• 作为产物：
  描述：

  2,3-二溴丙酰胺 在 氨 作用下， 以 二甲基亚砜 为溶剂， 生成 2-carbamoylaziridine
  参考文献：
  名称：

  吡啶溶液中的氟化氢与-cyano-2和-amido-2-aziridines的反应。通过β-氟-α-氨基腈和/或β-氟-α-氨基酸酰胺的酸性水解和醇解制备β-氟α-氨基酸和酯

  摘要：

  已研究了将吡啶鎓聚氟化氢（奥拉试剂）产生的氟化氢添加到某些-2-氰基和-2-氨基氮丙啶上。

  DOI：

  10.1016/s0022-1139(00)85554-2

文献信息

• Regioselective Ring Opening of N-H-Aziridines with Sulfur Nucleophiles in Liquid SO2
  作者：Māris Turks、Jevgeņija Lugiņina

  DOI：10.1055/s-0036-1588670

  日期：——

  N-H-Aziridines undergo efficient ring-opening reactions with aromatic and aliphatic thiols in liquid sulfur dioxide as reaction medium. Due to the Lewis acidic nature of SO2, these reactions do not require any other catalytic additives. The expected β-alkyl/arylthio-amines (β-amino thioethers) are obtained with excellent β-regioselectivity. The developed reaction conditions are compatible with chiral starting

  NH-氮丙啶与芳香族和脂肪族硫醇在液态二氧化硫作为反应介质中进行有效的开环反应。由于 SO2 的路易斯酸性，这些反应不需要任何其他催化添加剂。以优异的 β-区域选择性获得了预期的 β-烷基/芳硫基胺（β-氨基硫醚）。所开发的反应条件与手性原料相容，其对映体纯度在相应的产品中得以保留。该方法也可用于直接合成碳水化合物-氨基酸结合物和 2-亚氨基噻唑烷衍生物。
• Aziridine-2-carboxylic acid derivatives and its open-ring isomers as a novel PDIA1 inhibitors
  作者：Irena Leite、Victor Andrianov、Diana Zelencova-Gopejenko、Einars Loza、Iveta Kazhoka-Lapsa、Ilona Domracheva、Marta Stoyak、Stefan Chlopicki、Ivars Kalvins

  DOI：10.1007/s10593-021-03034-x

  日期：2021.11

  Acyl derivatives of aziridine-2-carboxylic acid have been synthesized and tested as PDIA1 inhibitors. Calculations of charge value and distribution in aziridine ring system and some alkylating agents were performed. For the first time was found that acyl derivatives of aziridine-2-carboxylic acid are weak to moderately active PDIA1 inhibitors.

  氮丙啶-2-羧酸的酰基衍生物已被合成并作为 PDIA1 抑制剂进行测试。进行了氮丙啶环系统和一些烷化剂的电荷值和分布的计算。首次发现氮丙啶-2-羧酸的酰基衍生物是弱到中等活性的PDIA1抑制剂。
• 1-Aziridine carboxylic acid derivatives with immunostimulant activity
  申请人：Boehringer Mannheim GmbH

  公开号：US04376731A1

  公开（公告）日：1983-03-15

  2-Substituted-1-aziridine-carboxylic acid esters exhibiting immuno-stimulant activity and of the formula ##STR1## wherein X is a carbamoyl or alkoxycarbonyl radical, and R.sup.1 is an aliphatic hydrocarbon radical optionally substituted by halogen, alkoxy, amino, carbamoyloxy, cycloalkyl, hydroxyl, an imido or heterocyclic radical, cycloalkyl; or aryl, aralkyl, aryloxyalkyl or arylthioalkyl wherein the aryl moiety is optionally substituted by halogen, alkyl, alkoxy, hydroxyl, amino, nitro, cyano, acyl, carbalkoxy, thioalkyl, alkylsulphonyl, phenyl or trifluoromethyl. Counterparts where X is --CN and R.sup.1 is as above, except for ethyl, are also new.

  2-取代-1-氮杂环丙酸酯具有免疫刺激活性，化学式为##STR1##其中X是一个氨基甲酰基或烷氧羰基基团，R.sup.1是一个脂肪烃基，可选择地被卤素、烷氧基、氨基、氨基甲酰氧基、环烷基、羟基、亚胺基或杂环基团、环烷基；或芳基、芳基烷基、芳基氧基烷基或芳基硫基烷基，其中芳基部分可选择地被卤素、烷基、烷氧基、羟基、氨基、硝基、氰基、酰基、羧烷氧基、硫基烷基、烷基磺酰基、苯基或三氟甲基取代。其中X为--CN且R.sup.1如上所述，除了乙基，也是新的。
• Access to NH-aziridine-2-carboxamides through Davidsen acylimidodicarbonate activation
  作者：Jekaterīna Ivanova、Boriss Štrumfs、Raivis Žalubovskis

  DOI：10.1016/j.crci.2019.03.001

  日期：2019.4

  Résumé Acylimidodicarbonates obtained from aziridine-2-carboxamides through Davidsen bis-Boc activation react with amine nucleophiles under mild conditions to form tertiary aziridine-2-carboxylic acid amides. NH aziridine-2-carboxylic acid amides were obtained by hydrogenolythic deprotection of N-Cbz derivatives. Supplementary Materials: Supplementary material for this article is supplied as a separate file: mmc1.doc

  简历 由氮杂环丙烷-2-羧酰胺通过Davidsen双Boc活化得到的乙酰氯代双碳酸酯，在温和条件下与胺类亲核试剂反应，生成三取代的氮杂环丙烷-2-羧酸酰胺。通过氢解去保护N-苄氧羰基衍生物，得到了NH型的氮杂环丙烷-2-羧酸酰胺。 补充材料： 本文的补充材料以单独文件形式提供： mmc1.doc
• 2-Substituted Penems with Amino Acid-Related Side Chains: Synthesis and Antibacterial Activity of a New Series of .beta.-Lactam Antibiotics
  作者：Maria Altamura、Enzo Perrotta、Piero Sbraci、Vittorio Pestellini、Federico Arcamone、Giuseppe Cascio、Laura Lorenzi、Giuseppe Satta、Grazia Morandotti、Roberta Sperning

  DOI：10.1021/jm00021a013

  日期：1995.10

  A new series of 6-(hydroxyethyl)penems 2-substituted with amino acid-related side chains was synthesized. The nature of the amino acyl derivative proved to be crucial both from a synthetic point of view, as beta-lactam ring opening can compete with C-2 nucleophilic substitution, and for antibacterial activity. Primary amino acid amides emerged as the most suitable side chains for enhancing permeability

  合成了一系列新的6-（羟乙基）青霉烯2-氨基酸相关的侧链取代。从合成的观点来看，氨基酰基衍生物的性质被证明是至关重要的，因为β-内酰胺开环可以与C-2亲核取代竞争，并且具有抗菌活性。伯氨基酸酰胺作为增强通过革兰氏阴性外膜渗透性的最合适的侧链出现。新的2-[（（氨基酰胺基）甲基]青霉烯3a-u）的体外活性受酰胺部分的性质和位置，环状酰胺的环大小以及氨基酸构型的影响。