N'-(o-fluorophenyl)acetamidine | 87356-46-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N'-(o-fluorophenyl)acetamidine
• 英文别名: Ethanimidamide, N-(2-fluorophenyl)-；N'-(2-fluorophenyl)ethanimidamide
• CAS: 87356-46-5
• 化学式: C₈H₉FN₂
• 分子量: 152.171
• InChiKey: GJFYEWVFFROKKM-UHFFFAOYSA-N

物化性质

• 熔点：
  99.8-100.7 °C
• 沸点：
  184.9±42.0 °C(Predicted)
• 密度：
  1.11±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  38.4
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-丁炔酸乙酯 、 N'-(o-fluorophenyl)acetamidine 以 乙醇 为溶剂， 反应 96.0h， 以56%的产率得到3-(2-fluorophenyl)-2,6-dimethyl-4(3H)-pyrimidinone
  参考文献：
  名称：

  Gupta, K. A.; Saxena, Anil K.; Jain, Padam C., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1983, vol. 22, # 4, p. 384 - 387

  摘要：

  DOI：
• 作为产物：
  描述：

  2-氟碘苯 、 盐酸乙脒 在 copper(l) iodide 、 caesium carbonate 作用下， 以 乙腈 为溶剂， 反应 24.0h， 以47%的产率得到N'-(o-fluorophenyl)acetamidine
  参考文献：
  名称：

  Ligand-Free Copper-Catalyzed Arylation of Amidines

  摘要：

  Copper-catalyzed cross-coupling reactions of amidine salts were utilized to synthesize monoarylated amidines in moderate to high yields with ligand-free conditions. DMF was the superior solvent for the N-arylation of benzamidines, while MeCN was used in the formation of N-aryl amidines in moderate to high yield.

  DOI：

  10.1021/jo102235u

文献信息

• Rh(III)-Catalyzed Synthesis of <i>N</i>-Unprotected Indoles from Imidamides and Diazo Ketoesters via C–H Activation and C–C/C–N Bond Cleavage
  作者：Zisong Qi、Songjie Yu、Xingwei Li

  DOI：10.1021/acs.orglett.5b03669

  日期：2016.2.19

  The synthesis of N-unprotected indoles has been realized via Rh(III)-catalyzed C–H activation/annulation of imidamides with α-diazo β-ketoesters. The reaction occurs with the release of an amide coproduct, which originates from both the imidamide and the diazo as a result of C═N cleavage of the imidamide and C–C(acyl) cleavage of the diazo. A rhodacyclic intermediate has been isolated and a plausible

  N-未保护的吲哚的合成已通过Rh（III）催化的C-H活化/亚酰胺与α-重氮β-酮酸酯的环化而实现。反应发生时会发生酰胺副产物的释放，酰胺副产物既来自亚酰胺也来自重氮，这是由于亚胺的C═N裂解和重氮的C–C（酰基）裂解所致。分离了一个rhodocyclic中间体，并提出了一个合理的机制。
• Ruthenium(II)‐Catalyzed C−H Activation of Imidamides and Divergent Couplings with Diazo Compounds: Substrate‐Controlled Synthesis of Indoles and 3 <i>H</i> ‐Indoles
  作者：Yunyun Li、Zisong Qi、He Wang、Xifa Yang、Xingwei Li

  DOI：10.1002/anie.201606316

  日期：2016.9.19

  Indoles are an important structural motif that is commonly found in biologically active molecules. In this work, conditions for divergent couplings between imidamides and acceptor–acceptor diazo compounds were developed that afforded NH indoles and 3H‐indoles under ruthenium catalysis. The coupling of α‐diazoketoesters afforded NH indoles by cleavage of the C(N2)−C(acyl) bond whereas α‐diazomalonates

  吲哚是生物活性分子中常见的重要结构基序。在这项工作中，开发了酰亚胺酰胺和受体-受体重氮化合物之间发散偶联的条件，该条件可在钌催化下提供NH吲哚和3 H-吲哚。α-二氮杂酮酸酯的偶联通过裂解C（N 2）-C（酰基）键提供了NH吲哚，而α-二氮杂丙二酸酯通过C-N键的裂解产生了3个H-吲哚。该反应通过钌催化的CH活化作用构成重氮底物与芳烃的第一个分子间偶联。
• Synthesis of 2-Substituted Quinolines <i>via</i> Rhodium(III)-Catalyzed C-H Activation of Imidamides and Coupling with Cyclopropanols
  作者：Xukai Zhou、Zisong Qi、Songjie Yu、Lingheng Kong、Yang Li、Wan-Fa Tian、Xingwei Li

  DOI：10.1002/adsc.201601278

  日期：2017.5.17

  An efficient synthesis of 2-substituted quinolines from readily available cyclopropanols and imidamides has been developed, where the cyclopropanol acts as a C3 synthon. With the assistance of a bifunctional imidamide directing group, the reaction occurred via sequential C–H/C–C cleavage and C–C/C–N bond formation.

  已经开发了从容易获得的环丙醇和酰亚胺酰胺有效合成2-取代的喹啉的方法，其中环丙醇充当C 3合成子。在双官能的酰亚胺酰胺导向基团的协助下，反应通过顺序的C–H / C–C裂解和C–C / C–N键形成而发生。
• GUPTA, K. A.;SAXENA, ANIL, K.;JAIN, PADAM, C.;SRIMAL, R. C.;KAR, K.;ANAND+, INDIAN J. CHEM., 1983, 22, N 4, 384-387
  作者：GUPTA, K. A.、SAXENA, ANIL, K.、JAIN, PADAM, C.、SRIMAL, R. C.、KAR, K.、ANAND+

  DOI：——

  日期：——
• Ligand-Free Copper-Catalyzed Arylation of Amidines
  作者：Michelle Cortes-Salva、Corey Garvin、Jon C. Antilla

  DOI：10.1021/jo102235u

  日期：2011.3.4

  Copper-catalyzed cross-coupling reactions of amidine salts were utilized to synthesize monoarylated amidines in moderate to high yields with ligand-free conditions. DMF was the superior solvent for the N-arylation of benzamidines, while MeCN was used in the formation of N-aryl amidines in moderate to high yield.