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

methyl 2-(4-trifluoromethyl-2-pyridyloxy)propionate | 605681-32-1

中文名称
——
中文别名
——
英文名称
methyl 2-(4-trifluoromethyl-2-pyridyloxy)propionate
英文别名
methyl 2-[4-(trifluoromethyl)pyridin-2-yl]oxypropanoate
methyl 2-(4-trifluoromethyl-2-pyridyloxy)propionate化学式
CAS
605681-32-1
化学式
C10H10F3NO3
mdl
——
分子量
249.19
InChiKey
JDQRTWPIXYPHKL-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):
    2.4
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    48.4
  • 氢给体数:
    0
  • 氢受体数:
    7

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

反应信息

  • 作为产物:
    描述:
    2-(4-trifluoromethyl-2-pyridyloxy)propionic acid三甲基硅烷化重氮甲烷 在 silica gel 、 乙酸乙酯正己烷 作用下, 以 二氯甲烷甲醇 为溶剂, 反应 0.25h, 以to give methyl 2-(4-trifluoromethyl-2-pyridyloxy)propionate, which的产率得到methyl 2-(4-trifluoromethyl-2-pyridyloxy)propionate
    参考文献:
    名称:
    Substituted amides
    摘要:
    结构式(I)的新化合物是Cannabinoid-1(CB1)受体的拮抗剂和/或反向激动剂,可用于治疗、预防和抑制由CB1受体介导的疾病。本发明的化合物可用作中枢作用药物,治疗精神病、记忆障碍、认知障碍、偏头痛、神经病、神经炎性疾病(包括多发性硬化和格林-巴利综合症)以及病毒性脑炎、脑血管意外和头部创伤的炎症后遗症、焦虑症、压力、癫痫、帕金森病、运动障碍和精神分裂症。这些化合物还可用于治疗物质滥用障碍,治疗肥胖症或进食障碍,以及治疗哮喘、便秘、慢性肠假性梗阻和肝硬化。
    公开号:
    US07576239B2
点击查看最新优质反应信息

文献信息

  • [EN] SUBSTITUTED AMIDES<br/>[FR] AMIDES SUBSTITUES
    申请人:MERCK & CO INC
    公开号:WO2003077847A2
    公开(公告)日:2003-09-25
    Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson s disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, and cirrhosis of the liver.
    结构式(I)的新型化合物是大麻素-1(CB1)受体的拮抗剂和/或反向激动剂,可用于治疗、预防和抑制由CB1受体介导的疾病。本发明的化合物可作为中枢作用药物,用于治疗精神病、记忆障碍、认知障碍、偏头痛、神经病、神经炎性疾病(包括多发性硬化和格林-巴利综合征)以及病毒性脑炎、脑血管意外和头部创伤的炎症后遗症、焦虑症、压力、癫痫、帕金森病、运动障碍和精神分裂症。这些化合物还可用于治疗物质滥用障碍、肥胖症或进食障碍,以及哮喘、便秘、慢性肠假性梗阻和肝硬化的治疗。
  • Substituted amides
    申请人:Lin S. Linus
    公开号:US20060106071A1
    公开(公告)日:2006-05-18
    Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, and cirrhosis of the liver.
    结构式(I)的新型化合物是大麻素-1(CB1)受体的拮抗剂和/或反向激动剂,可用于治疗、预防和抑制由CB1受体介导的疾病。本发明的化合物可作为中枢作用药物用于治疗精神病、记忆障碍、认知障碍、偏头痛、神经病、神经炎症性疾病(包括多发性硬化症和格林-巴利综合征)、病毒性脑炎、脑血管意外和头部创伤的炎症后遗症、焦虑症、压力、癫痫、帕金森病、运动障碍和精神分裂症。这些化合物还可用于治疗物质滥用障碍、肥胖症或进食障碍,以及哮喘、便秘、慢性肠梗阻和肝硬化的治疗。
  • Substituted pyridyoxy amides
    申请人:Merck & Co., Inc.
    公开号:US07550489B2
    公开(公告)日:2009-06-23
    Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, and cirrhosis of the liver.
    结构式(I)的新化合物是Cannabinoid-1(CB1)受体的拮抗剂和/或逆向激动剂,并且在治疗、预防和抑制由CB1受体介导的疾病方面是有用的。本发明的化合物可用作中枢作用药物,用于治疗精神病、记忆障碍、认知障碍、偏头痛、神经病、神经炎性疾病(包括多发性硬化症和吉兰-巴雷综合症)以及病毒性脑炎、脑血管意外和头部创伤的炎性后遗症、焦虑症、压力、癫痫、帕金森病、运动障碍和精神分裂症。该化合物还可用于治疗物质滥用障碍、肥胖症或进食障碍,以及哮喘、便秘、慢性肠假性梗阻和肝硬化的治疗。
  • WO2007/136571
    申请人:——
    公开号:——
    公开(公告)日:——
  • SUBSTITUTED AMIDES
    申请人:Merck Sharp & Dohme Corp.
    公开号:EP1496838B1
    公开(公告)日:2010-11-03
查看更多