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

N-methoxy-N-methyl-5-methyl-1,2,4-oxadiazole-3-carboxamide | 1104606-46-3

中文名称
——
中文别名
——
英文名称
N-methoxy-N-methyl-5-methyl-1,2,4-oxadiazole-3-carboxamide
英文别名
N-methoxy-N,5-dimethyl-1,2,4-oxadiazole-3-carboxamide
N-methoxy-N-methyl-5-methyl-1,2,4-oxadiazole-3-carboxamide化学式
CAS
1104606-46-3
化学式
C6H9N3O3
mdl
——
分子量
171.156
InChiKey
ISRYJDKTAJJXKK-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):
    0.4
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    68.5
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    1-甲基-4-碘-吡唑N-methoxy-N-methyl-5-methyl-1,2,4-oxadiazole-3-carboxamide异丙基氯化镁 作用下, 以 四氢呋喃 为溶剂, 反应 2.17h, 以88.4%的产率得到1-methyl-pyrazol-4-yl 5-methyl-1,2,4-oxadiazol-3-yl ketone
    参考文献:
    名称:
    生长抑素受体拮抗剂的路线开发和多千克GMP传递
    摘要:
    描述了MK-4256首次GMP交付的多公斤级路线开发和演示。聚合路线的关键方面包括区域选择性绿色碘化,一锅法合成恶二唑,有效的酮Pictet-Spengler反应以及通过结晶的非对映异构体升级,从而提供6 kg的API。回收程序可以从Pictet-Spengler反应中,从富含不需要的非对映异构体的非对映异构体混合物中增加所需非对映异构体的收率。
    DOI:
    10.1021/op300128c
  • 作为产物:
    描述:
    二甲羟胺盐酸盐5-甲基-1,2,4-噁二唑-3-羧酸钾盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 反应 1.67h, 以98%的产率得到N-methoxy-N-methyl-5-methyl-1,2,4-oxadiazole-3-carboxamide
    参考文献:
    名称:
    生长抑素受体拮抗剂的路线开发和多千克GMP传递
    摘要:
    描述了MK-4256首次GMP交付的多公斤级路线开发和演示。聚合路线的关键方面包括区域选择性绿色碘化,一锅法合成恶二唑,有效的酮Pictet-Spengler反应以及通过结晶的非对映异构体升级,从而提供6 kg的API。回收程序可以从Pictet-Spengler反应中,从富含不需要的非对映异构体的非对映异构体混合物中增加所需非对映异构体的收率。
    DOI:
    10.1021/op300128c
点击查看最新优质反应信息

文献信息

  • [EN] TRIAZOLE BETA CARBOLINE DERIVATIVES AS ANTIDIABETIC COMPOUNDS<br/>[FR] DÉRIVÉS DE LA BÊTA CARBOLINE TRIAZOLE CONSTITUANT DES COMPOSÉS ANTIDIABÉTIQUES
    申请人:MERCK SHARP & DOHME
    公开号:WO2010051177A1
    公开(公告)日:2010-05-06
    Beta-carboline derivatives of structural formula (I) are selective antagonists of the somatostatin subtype receptor 3 (SSTR3) and are useful for the treatment of Type 2 diabetes mellitus and of conditions that are often associated with this disease, including hyperglycemia, insulin resistance, obesity, lipid disorders, and hypertension. The compounds are also useful for the treatment of depression and anxiety.
    结构式(I)的β-咔啉衍生物是生长抑素亚型受体3 (SSTR3)的选择性拮抗剂,可用于治疗2型糖尿病以及通常与该疾病相关的病症,包括高血糖、胰岛素抵抗、肥胖、脂质紊乱和高血压。这些化合物还可用于治疗抑郁症和焦虑症。
  • BETA CARBOLINE DERIVATIVES AS ANTIDIABETIC COMPOUNDS
    申请人:Dobbelaar Peter H.
    公开号:US20100184758A1
    公开(公告)日:2010-07-22
    Beta-carboline derivatives of structural formula I are selective antagonists of the somatostatin subtype receptor 3 (SSTR3) and are useful for the treatment of Type 2 diabetes mellitus and of conditions that are often associated with this disease, including hyperglycemia, insulin resistance, obesity, lipid disorders, and hypertension. The compounds are also useful for the treatment of depression and anxiety.
    结构式I的β-咔啉衍生物是生长抑素亚型受体3(SSTR3)的选择性拮抗剂,可用于治疗2型糖尿病以及通常与该疾病相关的病症,包括高血糖、胰岛素抵抗、肥胖、脂质异常和高血压。这些化合物还可用于治疗抑郁症和焦虑症。
  • TRIAZOLE BETA CARBOLINE DERIVATIVES AS ANTI-DIABETIC AGENTS
    申请人:Guo Liangqin
    公开号:US20110201615A1
    公开(公告)日:2011-08-18
    Beta-carboline derivatives of structural formula (I) are selective antagonists of the somatostatin subtype receptor 3 (SSTR3) and are useful for the treatment of Type 2 diabetes mellitus and of conditions that are often associated with this disease, including hyperglycemia, insulin resistance, obesity, lipid disorders, and hypertension. The compounds are also useful for the treatment of depression and anxiety.
    结构式(I)的β-咔啉衍生物是生长抑素亚型受体3(SSTR3)的选择性拮抗剂,可用于治疗2型糖尿病以及常与该疾病相关的病症,包括高血糖、胰岛素抵抗、肥胖、脂质异常和高血压。这些化合物还可用于治疗抑郁症和焦虑症。
  • The Discovery of MK-4256, a Potent SSTR3 Antagonist as a Potential Treatment of Type 2 Diabetes
    作者:Shuwen He、Zhixiong Ye、Quang Truong、Shrenik Shah、Wu Du、Liangqin Guo、Peter H. Dobbelaar、Zhong Lai、Jian Liu、Tianying Jian、Hongbo Qi、Raman K. Bakshi、Qingmei Hong、James Dellureficio、Alexander Pasternak、Zhe Feng、Reynalda deJesus、Lihu Yang、Mikhail Reibarkh、Scott A. Bradley、Mark A. Holmes、Richard G. Ball、Rebecca T. Ruck、Mark A. Huffman、Frederick Wong、Koppara Samuel、Vijay B. Reddy、Stan Mitelman、Sharon X. Tong、Gary G. Chicchi、Kwei-Lan Tsao、Dorina Trusca、Margaret Wu、Qing Shao、Maria E. Trujillo、George J. Eiermann、Cai Li、Bei B. Zhang、Andrew D. Howard、Yun-Ping Zhou、Ravi P. Nargund、William K. Hagmann
    DOI:10.1021/ml300063m
    日期:2012.6.14
    A structure-activity relationship study of the imidazolyl-beta-tetrahydrocarboline series identified MK-4256 as a potent, selective SSTR3 antagonist, which demonstrated superior efficacy in a mouse oGTT model. MK-4256 reduced glucose excursion in a dose-dependent fashion with maximal efficacy achieved at doses as low as 0.03 mg/kg po. As compared with glipizide, MK-4256 showed a minimal hypoglycemia risk in mice.
  • [EN] BETA CARBOLINE DERIVATIVES AS ANTIDIABETIC COMPOUNDS<br/>[FR] DÉRIVÉS DE BÊTA-CARBOLINE EN TANT QUE COMPOSÉS ANTIDIABÉTIQUES
    申请人:MERCK & CO INC
    公开号:WO2009011836A1
    公开(公告)日:2009-01-22
    Beta-carboline derivatives of structural formula I are selective antagonists of the somatostatin subtype receptor 3 (SSTR3) and are useful for the treatment of Type 2 diabetes mellitus and of conditions that are often associated with this disease, including hyperglycemia, insulin resistance, obesity, lipid disorders, and hypertension. The compounds are also useful for the treatment of depression and anxiety.
查看更多

同类化合物

伊莫拉明 (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5-氨基-1,3,4-噻二唑-2-基)甲醇 齐墩果-2,12-二烯[2,3-d]异恶唑-28-酸 黄曲霉毒素H1 高效液相卡套柱 非昔硝唑 非布索坦杂质Z19 非布索坦杂质T 非布索坦杂质K 非布索坦杂质E 非布索坦杂质67 非布索坦杂质65 非布索坦杂质64 非布索坦杂质61 非布索坦代谢物67M-4 非布索坦代谢物67M-2 非布索坦代谢物 67M-1 非布索坦-D9 非布索坦 非唑拉明 雷西纳德杂质H 雷西纳德 阿西司特 阿莫奈韦 阿米苯唑 阿米特罗13C2,15N2 阿瑞匹坦杂质 阿格列扎 阿扎司特 阿尔吡登 阿塔鲁伦中间体 阿培利司N-1 阿哌沙班杂质26 阿哌沙班杂质15 阿可替尼 阿作莫兰 阿佐塞米 镁(2+)(Z)-4'-羟基-3'-甲氧基肉桂酸酯 锌1,2-二甲基咪唑二氯化物 铵2-(4-氯苯基)苯并恶唑-5-丙酸盐 铬酸钠[-氯-3-[(5-二氢-3-甲基-5-氧代-1-苯基-1H-吡唑-4-基)偶氮]-2-羟基苯磺酸基][4-[(3,5-二氯-2-羟基苯 铁(2+)乙二酸酯-3-甲氧基苯胺(1:1:2) 钠5-苯基-4,5-二氢吡唑-1-羧酸酯 钠3-[2-(2-壬基-4,5-二氢-1H-咪唑-1-基)乙氧基]丙酸酯 钠3-(2H-苯并三唑-2-基)-5-仲-丁基-4-羟基苯磺酸酯 钠(2R,4aR,6R,7R,7aS)-6-(2-溴-9-氧代-6-苯基-4,9-二氢-3H-咪唑并[1,2-a]嘌呤-3-基)-7-羟基四氢-4H-呋喃并[3,2-D][1,3,2]二氧杂环己膦烷e-2-硫醇2-氧化物 野麦枯 野燕枯 醋甲唑胺