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2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-oxoethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one | 1224172-15-9

中文名称
——
中文别名
——
英文名称
2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-oxoethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one
英文别名
2-(4-chlorophenyl)-5-[4-(2-cyclopropyl-2-oxoethoxy)-3-methoxyphenyl]-6H-pyrrolo[3,4-d]triazol-4-one
2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-oxoethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one化学式
CAS
1224172-15-9
化学式
C22H19ClN4O4
mdl
——
分子量
438.87
InChiKey
ZBHDKEOCEGWNLY-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):
    3.6
  • 重原子数:
    31
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    86.6
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-oxoethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one 在 sodium tetrahydroborate 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 12.0h, 以86%的产率得到2-(4-chlorophenyl)-5-(4-(2-cyclopropyl-2-hydroxyethoxy)-3-methoxyphenyl)-5,6-dihydropyrrolo[3,4-d][1,2,3]triazol-4(2H)-one
    参考文献:
    名称:
    Dihydropyrrolopyrazol-6-one MCHR1 antagonists for the treatment of obesity: Insights on in vivo efficacy from a novel FLIPR assay setup
    摘要:
    Our investigation of the structure-activity and structure-liability relationships for dihydropyrrolopyrazol-6-one MCHR1 antagonists revealed that off-rate characteristics, inferred from potencies in a FLIPR assay following a 2 h incubation, can impact in vivo efficacy. The in vitro and exposure profiles of dihydropyrrolopyrazol-6-ones 1b and 1e were comparable to that of the thienopyrimidinone counterparts 41 and 43 except for a much faster MCHR1 apparent off-rate. The greatly diminished dihydropyrrolopyrazol-6-one anti-obesity response may be the consequence of this rapid off-rate. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2015.05.008
  • 作为产物:
    参考文献:
    名称:
    Dihydropyrrolopyrazol-6-one MCHR1 antagonists for the treatment of obesity: Insights on in vivo efficacy from a novel FLIPR assay setup
    摘要:
    Our investigation of the structure-activity and structure-liability relationships for dihydropyrrolopyrazol-6-one MCHR1 antagonists revealed that off-rate characteristics, inferred from potencies in a FLIPR assay following a 2 h incubation, can impact in vivo efficacy. The in vitro and exposure profiles of dihydropyrrolopyrazol-6-ones 1b and 1e were comparable to that of the thienopyrimidinone counterparts 41 and 43 except for a much faster MCHR1 apparent off-rate. The greatly diminished dihydropyrrolopyrazol-6-one anti-obesity response may be the consequence of this rapid off-rate. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2015.05.008
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文献信息

  • AZOLOPYRROLONE MELANIN CONCENTRATING HORMONE RECEPTOR-1 ANTAGONISTS
    申请人:Devasthale Pratik
    公开号:US20110195934A1
    公开(公告)日:2011-08-11
    The present application provides compounds, including all stereoisomers, solvates, prodrugs and pharmaceutically acceptable faints thereof according to wherein all of the variables are defined herein.
    本申请提供了化合物,包括所有立体异构体、溶剂化物、前药和药学上可接受的盐,其中所有变量在此定义。
  • [EN] AZOLOPYRROLONE MELANIN CONCENTRATING HORMONE RECEPTOR-1 ANTAGONISTS<br/>[FR] ANTAGONISTES DE RÉCEPTEUR-1 DE L'HORMONE DE MÉLANO-CONCENTRATION D'AZOLOPYRROLONE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2010047956A9
    公开(公告)日:2011-10-06
  • US8415386B2
    申请人:——
    公开号:US8415386B2
    公开(公告)日:2013-04-09
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