tert-butyl N-[3-[bis[(2-methylpropan-2-yl)oxycarbonyl]amino]-3-oxopropyl]-N-(pyridin-2-ylmethyl)carbamate | 502510-14-7

• 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: tert-butyl N-[3-[bis[(2-methylpropan-2-yl)oxycarbonyl]amino]-3-oxopropyl]-N-(pyridin-2-ylmethyl)carbamate
• CAS: 502510-14-7
• 化学式: C₂₄H₃₇N₃O₇
• 分子量: 479.574
• InChiKey: ZUMNPDJVMNGRGF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  34
• 可旋转键数：
  11
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  115
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  tert-butyl N-[3-[bis[(2-methylpropan-2-yl)oxycarbonyl]amino]-3-oxopropyl]-N-(pyridin-2-ylmethyl)carbamate 在 盐酸 作用下， 以 乙醚 、 二氯甲烷 为溶剂， 反应 24.0h， 生成 [7-({3-[(Pyridin-2-ylmethyl)-amino]-propionylamino}-methyl)-6,9-dihydro-5H-benzocyclohepten-5-yl]-acetic acid
  参考文献：
  名称：

  Substituted benzocyloheptenes as potent and selective αv integrin antagonists

  摘要：

  A novel series of potent and specific alpha(v) integrin antagonists has been obtained by aminoalkyl substitutions on benzocyloheptene acetic acids as a rigid GD bioisostere. The preferred compounds 1-2, 1-3 and 1-8, showed nano- to subnanomolar IC50 values on alpha(v)beta(3) and alpha(v)beta(5) integrins, with favorable pharmacokinetics. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00696-0
• 作为产物：
  描述：

  2-氨甲基吡啶 以 叔丁醇 为溶剂， 反应 48.0h， 生成 tert-butyl N-[3-[bis[(2-methylpropan-2-yl)oxycarbonyl]amino]-3-oxopropyl]-N-(pyridin-2-ylmethyl)carbamate
  参考文献：
  名称：

  Substituted benzocyloheptenes as potent and selective αv integrin antagonists

  摘要：

  A novel series of potent and specific alpha(v) integrin antagonists has been obtained by aminoalkyl substitutions on benzocyloheptene acetic acids as a rigid GD bioisostere. The preferred compounds 1-2, 1-3 and 1-8, showed nano- to subnanomolar IC50 values on alpha(v)beta(3) and alpha(v)beta(5) integrins, with favorable pharmacokinetics. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(02)00696-0

文献信息

• US6846833B2
  申请人：——

  公开号：US6846833B2

  公开（公告）日：2005-01-25
• Substituted benzocyloheptenes as potent and selective αv integrin antagonists
  作者：Françoise Perron-Sierra、Dominique Saint Dizier、Marc Bertrand、Annie Genton、Gordon C Tucker、Patrick Casara

  DOI：10.1016/s0960-894x(02)00696-0

  日期：2002.11

  A novel series of potent and specific alpha(v) integrin antagonists has been obtained by aminoalkyl substitutions on benzocyloheptene acetic acids as a rigid GD bioisostere. The preferred compounds 1-2, 1-3 and 1-8, showed nano- to subnanomolar IC50 values on alpha(v)beta(3) and alpha(v)beta(5) integrins, with favorable pharmacokinetics. (C) 2002 Elsevier Science Ltd. All rights reserved.