摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-Chloro-6-(4-ethoxy-phenyl)-4,5,7-trimethyl-6H-pyrrolo[3,4-d]pyridazine | 647828-37-3

中文名称
——
中文别名
——
英文名称
1-Chloro-6-(4-ethoxy-phenyl)-4,5,7-trimethyl-6H-pyrrolo[3,4-d]pyridazine
英文别名
1-chloro-6-(4-ethoxyphenyl)-4,5,7-trimethyl-6H-pyrrolo[3,4-d]pyridazine;4-chloro-6-(4-ethoxyphenyl)-1,5,7-trimethylpyrrolo[3,4-d]pyridazine
1-Chloro-6-(4-ethoxy-phenyl)-4,5,7-trimethyl-6H-pyrrolo[3,4-d]pyridazine化学式
CAS
647828-37-3
化学式
C17H18ClN3O
mdl
——
分子量
315.802
InChiKey
QABJKSMARNNCQC-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

物化性质

  • 沸点:
    536.2±50.0 °C(Predicted)
  • 密度:
    1.24±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    39.9
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:0b82db48356e94585dbc097b9c17b4c1
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-氟苄胺1-Chloro-6-(4-ethoxy-phenyl)-4,5,7-trimethyl-6H-pyrrolo[3,4-d]pyridazine吡啶 、 N-methylmorpholine resin 作用下, 生成 N-(3-fluorobenzyl)-6-(4-ethoxyphenyl)-4,5,7-trimethyl-6H-pyrrolo[3,4-d]pyridazin-1-amine
    参考文献:
    名称:
    对电压门控钙通道的alpha(2)delta亚基的高亲和力配体的SAR研究加速:使用溶液相Sn2Ar耦合方法生成聚焦库。
    摘要:
    快速探索了铅化合物3的SAR,它是电压门控钙通道的α(2)δ亚基的新型配体。利用平行溶液相Sn2Ar耦合方法,获得了一个聚焦库。该文库在体外进行了评估,并提供了一系列具有增强效价的类似物。还描述了库的SAR趋势。
    DOI:
    10.1016/j.bmcl.2005.08.117
  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological evaluation of 6-aryl-6 H -pyrrolo[3,4- d ]pyridazine derivatives: high-affinity ligands to the α 2 δ subunit of voltage gated calcium channels
    摘要:
    A novel class of 6-aryl-6H-pyrrolo[3,4-d]pyridazine ligands for the alpha(2)delta subunit of voltage-gated calcium channels has been described. Substitutions in the aryl ring of the molecule were generally not tolerated, and resulted in diminished binding to the alpha(2)delta subunit. Modifications to the pyridazine ring revealed numerous permissive substitutions, and detailed SAR studies were carried out in this portion of the molecule. Replacement of the pyridazine ring methyl group with an aminomethyl functionality provided greatly improved potency over the initial lead. The initial lead compound displayed good rat pharmacokinetic properties, and was shown to be efficacious in the Chung model for neuropathic pain in rats. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2003.12.036
点击查看最新优质反应信息

文献信息

  • Treatment of neuropathic pain with 6h-pyrrolo[3,4-d]pyridazine compounds
    申请人:Anker Burke Naomi
    公开号:US20060154929A1
    公开(公告)日:2006-07-13
    6H-pyrrolo[3,4-d]pyridazine compounds and methods of their use of as ligands of voltage gated calcium channels (VGCC), useful in the treatment of neuropathic pain, and psychiatric and mood disorders such as, for example, schizophrenia, anxiety, depression, panic, and bipolar disorder, as well as in the treatment of pain, Parkinson's disease, cognitive dysfunction, epilepsy, circadian rhythm disorders, drug addiction, drug abuse, drug withdrawal and other.
    6H-吡咯并[3,4-d]吡嗪化合物及其作为电压门控通道(VGCC)配体的使用方法,可用于治疗神经病性疼痛、精神和情绪障碍,例如精神分裂症、焦虑、抑郁、惊恐和双相情感障碍,以及治疗疼痛、帕森病、认知功能障碍、癫痫、昼夜节律紊乱、药物成瘾、药物滥用、戒断症状等。
  • Treatment of neuropathic pain with 6H-pyrrolo[3,4-d]pyridazine compounds
    申请人:Merck & Co. Inc.
    公开号:US07465730B2
    公开(公告)日:2008-12-16
    6H-pyrrolo[3,4-d]pyridazine compounds and methods of their use of as ligands of voltage gated calcium channels (VGCC), useful in the treatment of neuropathic pain, and psychiatric and mood disorders such as, for example, schizophrenia, anxiety, depression, panic, and bipolar disorder, as well as in the treatment of pain, Parkinson's disease, cognitive dysfunction, epilepsy, circadian rhythm disorders, drug addiction, drug abuse, drug withdrawal and other.
    6H-吡咯并[3,4-d]吡嗪化合物及其作为电压门控通道(VGCC)配体的应用方法,可用于治疗神经病理性疼痛和精神和情绪障碍,例如精神分裂症、焦虑、抑郁、恐慌和躁症,以及治疗疼痛、帕森氏病、认知功能障碍、癫痫、昼夜节律紊乱、药物成瘾、药物滥用、药物戒断等。
  • TREATMENT OF NEUROPATHIC PAIN WITH 6H-PYRROLO(3,4-D)PYRIDAZINE COMPOUNDS
    申请人:Merck & Co., Inc.
    公开号:EP1539168A2
    公开(公告)日:2005-06-15
  • US7465730B2
    申请人:——
    公开号:US7465730B2
    公开(公告)日:2008-12-16
  • [EN] TREATMENT OF NEUROPATHIC PAIN WITH 6H-PYRROLO[3,4-D]PYRIDAZINE COMPOUNDS<br/>[FR] TRAITEMENT DE LA DOULEUR NEUROPATHIQUE AU MOYEN DE COMPOSES 6H-PYRROLO[3,4-D]PYRIDAZINE
    申请人:MERCK & CO INC
    公开号:WO2004006836A2
    公开(公告)日:2004-01-22
    6H-pyrrolo[3,4-d]pyridazine compounds and methods of their use of as ligands of voltage gated calcium channels (VGCC), useful in the treatment of neuropathic pain, and psychiatric and mood disorders such as, for example, schizophrenia, anxiety, depression, panic, and bipolar disorder, as well as in the treatment of pain, Parkinson s disease, cognitive dysfunction, epilepsy, circadian rhythm disorders, drug addiction, drug abuse, drug withdrawal and other
查看更多