7,10-bis(4-fluorobenzyl)-2,2,4,4-tetrachloro-1,3,5,7,10-pentaaza-2λ5,4λ5,6λ5-triphosphaspiro[4.5]deca-1,3,5-triene | 1344673-99-9

• 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: 7,10-bis(4-fluorobenzyl)-2,2,4,4-tetrachloro-1,3,5,7,10-pentaaza-2λ5,4λ5,6λ5-triphosphaspiro[4.5]deca-1,3,5-triene
• 英文别名: 7,7,9,9-Tetrachloro-1,4-bis[(4-fluorophenyl)methyl]-1,4,6,8,10-pentaza-5lambda5,7lambda5,9lambda5-triphosphaspiro[4.5]deca-5(10),6,8-triene；7,7,9,9-tetrachloro-1,4-bis[(4-fluorophenyl)methyl]-1,4,6,8,10-pentaza-5λ5,7λ5,9λ5-triphosphaspiro[4.5]deca-5(10),6,8-triene
• CAS: 1344673-99-9
• 化学式: C₁₆H₁₆Cl₄F₂N₅P₃
• 分子量: 551.067
• InChiKey: XCTDCOKAKRGVNG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.1
• 重原子数：
  30
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  43.6
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  7,10-bis(4-fluorobenzyl)-2,2,4,4-tetrachloro-1,3,5,7,10-pentaaza-2λ5,4λ5,6λ5-triphosphaspiro[4.5]deca-1,3,5-triene 、 4-哌啶酮缩乙二醇 在 三乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 31.0h， 以75%的产率得到7,10-bis(4-fluorobenzyl)-2,2,4,4-tetra-1,4-dioxa-8-azaspiro[4.5]dec-8-yl-1,3,5,7,10-pentaaza-2λ5,4λ5,6λ5-triphosphaspiro[4.5]deca-1,3,5-triene
  参考文献：
  名称：

  Phosphorus–nitrogen compounds part 22. Syntheses, structural investigations, biological activities and DNA interactions of new mono and bis (4-fluorobenzyl) spirocyclophosphazenes

  摘要：

  The reactions of hexachlorocyclotriphosphazene, N3P3Cl6, with mono (1 and 2) and bis(4-fluorobenzyl) diamines (3-5), FPhCH2NH(CH2)(n)NHR (R=H or FPhCH2-), produce mono (1a and 2a) and bis(4-fluorobenzyl) monospirocyclophosphazenes (3a-5a). The tetraaminomonospirocyclophosphazenes (1b-2d) are obtained from the reactions of the partly substituted phosphazenes (1a and 2a) with excess pyrrolidine, morpholine and 1,4-dioxa-8-azaspiro[4,5]decane (DASD), respectively. The tetrachlorobis(4-fluorobenzyl) monospirocyclophosphazenes (4a and 5a) with excess pyrrolidine, morpholine and DASD afford the fully substituted bis(4-fluorobenzyl) monospirocyclophosphazenes (4b, 4d-5d) in boiling THF. In addition, monochlorobis(4-fluorobenzyl) monospirocyclophosphazenes (4e and 41) have also been isolated from the reactions with excess morpholine and DASD in boiling THF. The structural investigations of the compounds have been verified by elemental analyses, MS. FTIR, H-1, C-13, F-19 (for 1d and 2d). P-31 NMR, HSQC and HMBC techniques. The crystal structures of 3a, 4a, 5a and 2b have been determined by X-ray crystallography. The compounds 2a-5a, 1b-2d, 4b, 4d-5d, 4e and 41 have been screened for antibacterial effects on bacteria and for antifungal activity against yeast strains. The compounds 1b and 4b showed antimicrobial activity against three species of bacteria, Bacillus subtilis, Bacillus cereus and Staphylococcus aureus, and two fungi, Candida albicans and Candida tropicalis. Minimum inhibitory concentrations (MIC) were determined for 1b and 4b. The MIC values were found to be 5000 mu M for each bacteria. The most effective compound, 4b has exhibited activity with a MIC of 312 mu M for C albicans and 625 mu M for C. tropicalis. DNA-binding and the nature of the interaction with pBR322 plasmid DNA are studied. All of the compounds induce changes on the DNA mobility and intensity. Prevention of Hind[l] digestion with the compounds indicates that the compounds bind with AT nucleotides in DNA. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2011.08.035
• 作为产物：
  描述：

  N¹,N²-bis(4-fluorobenzyl)ethane-1,2-diamine 在 六氯环三磷腈 、 三乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 26.0h， 以74%的产率得到7,10-bis(4-fluorobenzyl)-2,2,4,4-tetrachloro-1,3,5,7,10-pentaaza-2λ5,4λ5,6λ5-triphosphaspiro[4.5]deca-1,3,5-triene
  参考文献：
  名称：

  Phosphorus–nitrogen compounds part 22. Syntheses, structural investigations, biological activities and DNA interactions of new mono and bis (4-fluorobenzyl) spirocyclophosphazenes

  摘要：

  The reactions of hexachlorocyclotriphosphazene, N3P3Cl6, with mono (1 and 2) and bis(4-fluorobenzyl) diamines (3-5), FPhCH2NH(CH2)(n)NHR (R=H or FPhCH2-), produce mono (1a and 2a) and bis(4-fluorobenzyl) monospirocyclophosphazenes (3a-5a). The tetraaminomonospirocyclophosphazenes (1b-2d) are obtained from the reactions of the partly substituted phosphazenes (1a and 2a) with excess pyrrolidine, morpholine and 1,4-dioxa-8-azaspiro[4,5]decane (DASD), respectively. The tetrachlorobis(4-fluorobenzyl) monospirocyclophosphazenes (4a and 5a) with excess pyrrolidine, morpholine and DASD afford the fully substituted bis(4-fluorobenzyl) monospirocyclophosphazenes (4b, 4d-5d) in boiling THF. In addition, monochlorobis(4-fluorobenzyl) monospirocyclophosphazenes (4e and 41) have also been isolated from the reactions with excess morpholine and DASD in boiling THF. The structural investigations of the compounds have been verified by elemental analyses, MS. FTIR, H-1, C-13, F-19 (for 1d and 2d). P-31 NMR, HSQC and HMBC techniques. The crystal structures of 3a, 4a, 5a and 2b have been determined by X-ray crystallography. The compounds 2a-5a, 1b-2d, 4b, 4d-5d, 4e and 41 have been screened for antibacterial effects on bacteria and for antifungal activity against yeast strains. The compounds 1b and 4b showed antimicrobial activity against three species of bacteria, Bacillus subtilis, Bacillus cereus and Staphylococcus aureus, and two fungi, Candida albicans and Candida tropicalis. Minimum inhibitory concentrations (MIC) were determined for 1b and 4b. The MIC values were found to be 5000 mu M for each bacteria. The most effective compound, 4b has exhibited activity with a MIC of 312 mu M for C albicans and 625 mu M for C. tropicalis. DNA-binding and the nature of the interaction with pBR322 plasmid DNA are studied. All of the compounds induce changes on the DNA mobility and intensity. Prevention of Hind[l] digestion with the compounds indicates that the compounds bind with AT nucleotides in DNA. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.poly.2011.08.035

文献信息

• Phosphorus-nitrogen compounds. Part 67. The reactions of Mono/bis (4-fluorobenzyl)spiro(N/N)cyclotriphosphazenes with sodium(3-amino-1-propanoxide): investigation of spectral properties, DNA-cleavage and antimicrobial activities
  作者：Aytuğ Okumuş、Gamze Elmas、Zeynel Kılıç、Lütfiye Yasemin Gönder、Leyla Açık

  DOI：10.1080/10426507.2022.2145477

  日期：2023.3.4

  R2=FPhCH2-] (4-fluorobenzyl)monospiro(N/N)cyclotriphosphazenes, were obtained from the condensation reactions of hexachlorocyclotriphosphazatriene (N3P3Cl6; trimer; HCCP) with N-(4-fluorobenzyl)propane-1,3-diamine (L1), N,N'-bis(4-fluorobenzyl)propane-1,3-diamine (L2) and N,N'-bis(4-fluorobenzyl)ethane-1,2-diamine (L3), respectively. Substitution reactions of 1 and 2 with excess sodium(3-amino-1-propanoxide)

  摘要 起始试剂四氯单- [ 1 ; R 1 =(CH 2 ) 3 , R 2 =H]和四氯双-[ 2 ; R 1 =(CH 2 ) 3 , R 2 =FPhCH 2 - 和3 ; R 1 =(CH 2 ) 2 , R 2 =FPhCH 2 -](4-氟苄基)单螺环(N/N)环三磷腈，由六氯环三磷杂三烯(N 3 P 3 Cl 6 ;三聚体; HCCP )缩合得到) 与N -(4-氟苄基)丙烷-1,3-二胺 ( L1 ), N , N '-双(4-氟苄基)丙烷-1,3-二胺 ( L2 ) 和N , N '-双 (4 -fluorobenzyl)ethane-1,2-diamine ( L3 ), 分别。1和2与过量钠 (3-氨基-1-丙醇) 的取代反应分别产生唯一的单螺环 (N/O) 氨基-丙氧基-(4-氟苄基)螺环(N/N) ( 1a ) 和单螺环- ( N/O) 氨基丙氧基-双-(4-氟苄基)螺(N/N)
• Phosphorus-nitrogen compounds. Part 62. Preparation of tetraaminobis(4-fluorobenzyl)spiro(N/N)cyclotriphosphazenes: Chemical, structural characterizations, antimicrobial, antioxidant and DNA-binding activity studies
  作者：Aytuğ Okumuş、Gamze Elmas、Arzu Binici、Betül Aydın、Leyla Açık、Zeynel Kılıç、Tuncer Hökelek

  DOI：10.1016/j.ica.2022.121001

  日期：2022.8
• Phosphorus–nitrogen compounds part 22. Syntheses, structural investigations, biological activities and DNA interactions of new mono and bis (4-fluorobenzyl) spirocyclophosphazenes
  作者：Aytuğ Okumuş、Zeynel Kılıç、Tuncer Hökelek、Hakan Dal、Leyla Açık、Yağmur Öner、L. Yasemin Koç

  DOI：10.1016/j.poly.2011.08.035

  日期：2011.11

  The reactions of hexachlorocyclotriphosphazene, N3P3Cl6, with mono (1 and 2) and bis(4-fluorobenzyl) diamines (3-5), FPhCH2NH(CH2)(n)NHR (R=H or FPhCH2-), produce mono (1a and 2a) and bis(4-fluorobenzyl) monospirocyclophosphazenes (3a-5a). The tetraaminomonospirocyclophosphazenes (1b-2d) are obtained from the reactions of the partly substituted phosphazenes (1a and 2a) with excess pyrrolidine, morpholine and 1,4-dioxa-8-azaspiro[4,5]decane (DASD), respectively. The tetrachlorobis(4-fluorobenzyl) monospirocyclophosphazenes (4a and 5a) with excess pyrrolidine, morpholine and DASD afford the fully substituted bis(4-fluorobenzyl) monospirocyclophosphazenes (4b, 4d-5d) in boiling THF. In addition, monochlorobis(4-fluorobenzyl) monospirocyclophosphazenes (4e and 41) have also been isolated from the reactions with excess morpholine and DASD in boiling THF. The structural investigations of the compounds have been verified by elemental analyses, MS. FTIR, H-1, C-13, F-19 (for 1d and 2d). P-31 NMR, HSQC and HMBC techniques. The crystal structures of 3a, 4a, 5a and 2b have been determined by X-ray crystallography. The compounds 2a-5a, 1b-2d, 4b, 4d-5d, 4e and 41 have been screened for antibacterial effects on bacteria and for antifungal activity against yeast strains. The compounds 1b and 4b showed antimicrobial activity against three species of bacteria, Bacillus subtilis, Bacillus cereus and Staphylococcus aureus, and two fungi, Candida albicans and Candida tropicalis. Minimum inhibitory concentrations (MIC) were determined for 1b and 4b. The MIC values were found to be 5000 mu M for each bacteria. The most effective compound, 4b has exhibited activity with a MIC of 312 mu M for C albicans and 625 mu M for C. tropicalis. DNA-binding and the nature of the interaction with pBR322 plasmid DNA are studied. All of the compounds induce changes on the DNA mobility and intensity. Prevention of Hind[l] digestion with the compounds indicates that the compounds bind with AT nucleotides in DNA. (C) 2011 Elsevier Ltd. All rights reserved.