2-(2,4-dichlorophenyl)-1-{[(1-tert-butoxycarbonylpiperidin-4-yl)methyl]amino}-3-(1H-1,2,4-triazol-1-yl)propan-2-ol | 1119782-73-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 2-(2,4-dichlorophenyl)-1-{[(1-tert-butoxycarbonylpiperidin-4-yl)methyl]amino}-3-(1H-1,2,4-triazol-1-yl)propan-2-ol
• 英文别名: Tert-butyl 4-[[[2-(2,4-dichlorophenyl)-2-hydroxy-3-(1,2,4-triazol-1-yl)propyl]amino]methyl]piperidine-1-carboxylate
• CAS: 1119782-73-8
• 化学式: C₂₂H₃₁Cl₂N₅O₃
• 分子量: 484.426
• InChiKey: FXTVTBCEETWCEK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  32
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  92.5
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  2-(2,4-dichlorophenyl)-1-{[(1-tert-butoxycarbonylpiperidin-4-yl)methyl]amino}-3-(1H-1,2,4-triazol-1-yl)propan-2-ol 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 20.0h， 以69%的产率得到2-(2,4-dichlorophenyl)-1-[(piperidin-4-ylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ol
  参考文献：
  名称：

  Synthesis and structure–activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents

  摘要：

  Continuous efforts on the synthesis and structure-activity relationships (SARs) studies of modified 1-benzylamino-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents, allowed identification of new 1-[(pyridinyl- and piperidinylmethyl)amino] derivatives with MIC80 values ranging from 1410.0 to 23.0 ng mL (1) on Candida albicans. These results confirmed both the importance of pi-pi stacking and hydrogen bonding interactions in the active site of CYP51-C. albicans. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.11.101
• 作为产物：
  描述：

  1-Amino-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-1-yl)-2-propanol 、 1-叔丁氧羰基哌啶-4-甲醛 在 sodium cyanoborohydride 、 溶剂黄146 作用下， 以 甲醇 为溶剂， 反应 16.0h， 以26%的产率得到2-(2,4-dichlorophenyl)-1-{[(1-tert-butoxycarbonylpiperidin-4-yl)methyl]amino}-3-(1H-1,2,4-triazol-1-yl)propan-2-ol
  参考文献：
  名称：

  Synthesis and structure–activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents

  摘要：

  Continuous efforts on the synthesis and structure-activity relationships (SARs) studies of modified 1-benzylamino-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents, allowed identification of new 1-[(pyridinyl- and piperidinylmethyl)amino] derivatives with MIC80 values ranging from 1410.0 to 23.0 ng mL (1) on Candida albicans. These results confirmed both the importance of pi-pi stacking and hydrogen bonding interactions in the active site of CYP51-C. albicans. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.11.101

文献信息

• Synthesis and structure–activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents
  作者：Francis Giraud、Rémi Guillon、Cédric Logé、Fabrice Pagniez、Carine Picot、Marc Le Borgne、Patrice Le Pape

  DOI：10.1016/j.bmcl.2008.11.101

  日期：2009.1

  Continuous efforts on the synthesis and structure-activity relationships (SARs) studies of modified 1-benzylamino-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents, allowed identification of new 1-[(pyridinyl- and piperidinylmethyl)amino] derivatives with MIC80 values ranging from 1410.0 to 23.0 ng mL (1) on Candida albicans. These results confirmed both the importance of pi-pi stacking and hydrogen bonding interactions in the active site of CYP51-C. albicans. (C) 2008 Elsevier Ltd. All rights reserved.