tert-butyl 4-[(2S)-1-phenylmethoxycarbonylpyrrolidine-2-carbonyl]-1,4-diazepane-1-carboxylate | 479234-51-0

• 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 4-[(2S)-1-phenylmethoxycarbonylpyrrolidine-2-carbonyl]-1,4-diazepane-1-carboxylate
• CAS: 479234-51-0
• 化学式: C₂₃H₃₃N₃O₅
• 分子量: 431.532
• InChiKey: CRJSWWQHCKRBSX-IBGZPJMESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  31
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  79.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  tert-butyl 4-[(2S)-1-phenylmethoxycarbonylpyrrolidine-2-carbonyl]-1,4-diazepane-1-carboxylate 在 劳森试剂 、 盐酸 、 sodium cyanoborohydride 、 溶剂黄146 作用下， 以 1,4-二氧六环 、 甲醇 、 甲苯 为溶剂， 生成 benzyl (S)-2-(4-methyl-1,4-diazepane-1-carbonothioyl)pyrrolidine-1-carboxylate
  参考文献：
  名称：

  Non-peptide oxytocin agonists

  摘要：

  A library of compounds targeted to the vasopressin/oxytocin family of receptors was screened for activity at a cloned human oxytocin receptor using a reporter gene assay. Potency and selectivity were optimised to afford compound 39, EC50 = 33 nM. This series of compounds represents the first disclosed, non-peptide, low molecular weight agonists of the hormone oxytocin (OT). (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.04.107
• 作为产物：
  描述：

  1,4-二氮杂环庚烷-1-甲酸叔丁酯 、 N-苄氧羰基-L-脯氨酸 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 以100%的产率得到tert-butyl 4-[(2S)-1-phenylmethoxycarbonylpyrrolidine-2-carbonyl]-1,4-diazepane-1-carboxylate
  参考文献：
  名称：

  Non-peptide oxytocin agonists

  摘要：

  A library of compounds targeted to the vasopressin/oxytocin family of receptors was screened for activity at a cloned human oxytocin receptor using a reporter gene assay. Potency and selectivity were optimised to afford compound 39, EC50 = 33 nM. This series of compounds represents the first disclosed, non-peptide, low molecular weight agonists of the hormone oxytocin (OT). (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.04.107

文献信息

• Oxytocin agonists
  申请人：——

  公开号：US20040235753A1

  公开（公告）日：2004-11-25

  Compounds according to general formula 1, wherein G 1 is NR 6 R 7 or a group according to general formula 3 and G 2 NR 24 R 25 or a fused polycyclic group are novel. They are selective and potent oxytocin agonists. Pharmaceutical compositions of such compounds are useful in the treatment of, inter alia, erectile dysfunction. 1

  公式1中的化合物，其中G1是NR6R7或根据公式3的基团，G2是NR24R25或融合的多环基团，是新颖的选择性和有效的催产素激动剂。这些化合物的药物组成物在治疗勃起功能障碍等方面是有用的。
• OXYTOCIN AGONISTS
  申请人：Ferring BV

  公开号：EP1399436B1

  公开（公告）日：2005-03-16
• Non-peptide oxytocin agonists
  作者：Gary Pitt、Andrzej Batt、Robert Haigh、Andrew Penson、Peter Robson、David Rooker、André Tartar、Julie Trim、Christopher Yea、Michael Roe

  DOI：10.1016/j.bmcl.2004.04.107

  日期：2004.9

  A library of compounds targeted to the vasopressin/oxytocin family of receptors was screened for activity at a cloned human oxytocin receptor using a reporter gene assay. Potency and selectivity were optimised to afford compound 39, EC50 = 33 nM. This series of compounds represents the first disclosed, non-peptide, low molecular weight agonists of the hormone oxytocin (OT). (C) 2004 Elsevier Ltd. All rights reserved.