(3aS,4S,6R,6aR)-6-[6-Amino-2-(3-cyclopentyl-propionylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid ethylamide | 686768-40-1

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘌呤核苷
• 英文名称: (3aS,4S,6R,6aR)-6-[6-Amino-2-(3-cyclopentyl-propionylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid ethylamide
• CAS: 686768-40-1
• 化学式: C₂₃H₃₃N₇O₅
• 分子量: 487.559
• InChiKey: ATDMRHHDPCCRJU-KYFSNAEOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.87
• 重原子数：
  35.0
• 可旋转键数：
  7.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  155.51
• 氢给体数：
  3.0
• 氢受体数：
  10.0

反应信息

• 作为反应物：
  描述：

  (3aS,4S,6R,6aR)-6-[6-Amino-2-(3-cyclopentyl-propionylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid ethylamide 在 三氟乙酸 作用下， 反应 1.0h， 以60%的产率得到(2S,3S,4R,5R)-5-[6-amino-2-(3-cyclopentylpropanoylamino)purin-9-yl]-N-ethyl-3,4-dihydroxyoxolane-2-carboxamide
  参考文献：
  名称：

  2-(N-Acyl) and 2-N-acyl-N6-substituted analogues of adenosine and their affinity at the human adenosine receptors

  摘要：

  A series of 2-(N-acyl) and 2-(N-acyl)-N-6-alkyladenosine analogues have been synthesized from the intermediate 2-amino-6-chloroadenosine derivatives (2b and 7) and evaluated for their affinity at the human A(1), A(2A), and A(3) receptors. We found that 2-(N-acyl) derivatives of adenosine showed relatively low affinity at A(2A) and A(3) receptors, while the N-6-cyclopentyl substituent in 4h and 4i induced high potency [A(1) (K-i) = 20.7 and 31.8 nM respectively] at the A(1) receptor and resulted therefore in increased selectivity for this subtype. The general synthetic methods and their binding studies are presented herein. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.01.011
• 作为产物：
  描述：

  Acetic acid (3aR,4R,6R,6aR)-6-(2-amino-6-chloro-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 在 吡啶 、 4-二甲氨基吡啶 、 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 碘苯二乙酸 、 氨 、 水 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 反应 72.0h， 生成 (3aS,4S,6R,6aR)-6-[6-Amino-2-(3-cyclopentyl-propionylamino)-purin-9-yl]-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid ethylamide
  参考文献：
  名称：

  2-(N-Acyl) and 2-N-acyl-N6-substituted analogues of adenosine and their affinity at the human adenosine receptors

  摘要：

  A series of 2-(N-acyl) and 2-(N-acyl)-N-6-alkyladenosine analogues have been synthesized from the intermediate 2-amino-6-chloroadenosine derivatives (2b and 7) and evaluated for their affinity at the human A(1), A(2A), and A(3) receptors. We found that 2-(N-acyl) derivatives of adenosine showed relatively low affinity at A(2A) and A(3) receptors, while the N-6-cyclopentyl substituent in 4h and 4i induced high potency [A(1) (K-i) = 20.7 and 31.8 nM respectively] at the A(1) receptor and resulted therefore in increased selectivity for this subtype. The general synthetic methods and their binding studies are presented herein. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.01.011