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tert-butyl 8-chloro-6-fluoro-4-oxo-3,4-dihydrospiro[chromene-2,4'-piperidine]-1'-carboxylate | 1245738-46-8

中文名称
——
中文别名
——
英文名称
tert-butyl 8-chloro-6-fluoro-4-oxo-3,4-dihydrospiro[chromene-2,4'-piperidine]-1'-carboxylate
英文别名
tert-butyl 8-chloro-6-fluoro-4-oxo-3,4-dihydro-1'H-spiro[chromene-2,4'-piperidine]-1'-carboxylate
tert-butyl 8-chloro-6-fluoro-4-oxo-3,4-dihydrospiro[chromene-2,4'-piperidine]-1'-carboxylate化学式
CAS
1245738-46-8
化学式
C18H21ClFNO4
mdl
——
分子量
369.82
InChiKey
XQUNRBSCSULXFH-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.21
  • 重原子数:
    25.0
  • 可旋转键数:
    0.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    55.84
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    tert-butyl 8-chloro-6-fluoro-4-oxo-3,4-dihydrospiro[chromene-2,4'-piperidine]-1'-carboxylate 在 sodium tetrahydroborate 作用下, 以 乙醇 为溶剂, 反应 1.0h, 以87%的产率得到tert-butyl 8-chloro-6-fluoro-4-hydroxy-3,4-dihydrospiro[chromene-2,4'-piperidine]-1'-carboxylate
    参考文献:
    名称:
    Synthesis and pharmacological evaluation of novel N-aryl-3,4-dihydro-1′H-spiro[chromene-2,4′-piperidine]-1′-carboxamides as TRPM8 antagonists
    摘要:
    A novel series of N-aryl-3,4-dihydro-1'H-spiro[chromene-2,4'-piperidine]-1'-carboxamides was identified as transient receptor potential melastatin 8 (TRPM8) channel blockers through analogue-based rational design, synthesis and screening. Details of the synthesis, effect of aryl groups and their substituents on in-vitro potency were studied. The effects of selected functional groups on the 4-position of the chromene ring were also studied, which showed interesting results. The 4-hydroxy derivatives showed excellent potency and selectivity. Optical resolution and screening of alcohols revealed that (R)-(-)-isomers were in general more potent than the corresponding (S)-(+)-isomers. The isomer (R)-(-)-10e (IC50: 8.9 nM) showed a good pharmacokinetic profile upon oral dosing at 10 mg/kg in Sprague-Dawley (SD) rats. The compound (R)-(-)-10e also showed excellent efficacy in relevant rodent models of neuropathic pain. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.08.031
  • 作为产物:
    参考文献:
    名称:
    [EN] SPIROCYCLIC PIPERIDINE DERIVATIVES AS TRPM 8 MODULATORS
    [FR] DÉRIVÉS DE PIPÉRIDINE SPIROCYCLIQUES EN TANT QUE MODULATEURS DE TRPM8
    摘要:
    本发明提供了公式(I)的瞬时受体电位亚家族M,成员8(TRPM8)调节剂。特别地,本文所描述的化合物对于治疗或预防TRPM8调节的疾病,状况和/或紊乱非常有用。本文还提供了制备所述化合物的过程,用于其合成的中间体,其制药组合物以及用于治疗或预防由TRPM8调节的疾病,状况和/或紊乱的方法。
    公开号:
    WO2010103381A1
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