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2-[4-(4-Methoxy-benzyl)-5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl]-2-methyl-propionaldehyde

中文名称
——
中文别名
——
英文名称
2-[4-(4-Methoxy-benzyl)-5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl]-2-methyl-propionaldehyde
英文别名
2-[4-[(4-methoxyphenyl)methyl]-5-oxo-2,3-dihydro-1,4-benzoxazepin-8-yl]-2-methylpropanal
2-[4-(4-Methoxy-benzyl)-5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl]-2-methyl-propionaldehyde化学式
CAS
——
化学式
C21H23NO4
mdl
——
分子量
353.4
InChiKey
BMUPICRZMGEUBY-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):
    2.9
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    55.8
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 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-(4-Methoxy-benzyl)-5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl]-2-methyl-propionaldehyde三氟乙酸乙酸乙酯 在 silica 、 乙酸乙酯 、 crude residue 、 silica gel 、 hexanes 作用下, 以 正己烷 为溶剂, 反应 1.0h, 以to get 2-methyl-2-(5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl)-propionaldehyde (0.7 g, 70.6%) as white solid的产率得到2-Methyl-2-(5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl)-propionaldehyde
    参考文献:
    名称:
    INHIBITORS OF BRUTON'S TYROSINE KINASE
    摘要:
    本申请公开了按通用式(I)定义的化合物,其中所有变量如本文所述,可抑制BTK。本文所披露的化合物有助于调节BTK的活性,治疗与过度BTK活性有关的疾病。这些化合物还有助于治疗与异常B细胞增殖有关的炎症和自身免疫性疾病,如类风湿性关节炎。还披露了含有通式I的化合物和至少一种载体、稀释剂或赋形剂的组合物。
    公开号:
    US20150376166A1
  • 作为产物:
    描述:
    8-bromo-4-(4-methoxybenzyl)-3,4-dihydrobenzo[f]-[1,4]oxazepin-5(2H)-one 、 R-(+)-1,1'-联萘-2,2'-双二苯膦Dicaesio carbonate5-Brom-4-chlor-3-oxo-2,3-dihydro-pyridazin氯化铵醋酸钯 、 silica 、 乙酸乙酯 、 crude product 、 silica gel 、 正己烷 作用下, 以 1,4-二氧六环正己烷 为溶剂, 反应 16.08h, 以to get pure 2-[4-(4-methoxy-benzyl)-5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl]-2-methyl-propionaldehyde (1.0 g, 51.22%) as white solid的产率得到2-[4-(4-Methoxy-benzyl)-5-oxo-2,3,4,5-tetrahydro-benzo[f][1,4]oxazepin-8-yl]-2-methyl-propionaldehyde
    参考文献:
    名称:
    INHIBITORS OF BRUTON'S TYROSINE KINASE
    摘要:
    本申请公开了按通用式(I)定义的化合物,其中所有变量如本文所述,可抑制BTK。本文所披露的化合物有助于调节BTK的活性,治疗与过度BTK活性有关的疾病。这些化合物还有助于治疗与异常B细胞增殖有关的炎症和自身免疫性疾病,如类风湿性关节炎。还披露了含有通式I的化合物和至少一种载体、稀释剂或赋形剂的组合物。
    公开号:
    US20150376166A1
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文献信息

  • NOVEL HETEROCYCLIC FLUORESCENT DYES AND METHOD OF PRODUCTION THEREOF
    申请人:BASF SE
    公开号:EP2964704A1
    公开(公告)日:2016-01-13
  • US9663494B2
    申请人:——
    公开号:US9663494B2
    公开(公告)日:2017-05-30
  • [EN] NOVEL HETEROCYCLIC FLUORESCENT DYES AND METHOD OF PRODUCTION THEREOF<br/>[FR] NOUVEAUX COLORANTS FLUORESCENTS HÉTÉROCYCLIQUES ET LEUR PROCÉDÉ DE PRÉPARATION
    申请人:BASF SE
    公开号:WO2014135491A1
    公开(公告)日:2014-09-12
    The invention relates to novel compounds of formula (III) that can be used as heterocyclic dyes of unique structure and properties. These compounds can be obtained in a three-step synthesis from simple substrates. The compounds according to the invention have excellent solubility in organic solvents and excellent film-forming properties. In addition, high efficiency of energy conversion, excellent field-effect mobility, good on/off current ratios and/or excellent stability can be observed, when the compounds according to the invention are used in organic field effect transistors, organic photovoltaics (solar cells) and photodiodes.
  • [EN] INHIBITORS OF BRUTON'S TYROSINE KINASE<br/>[FR] INHIBITEURS DE LA TYROSINE KINASE DE BRUTON
    申请人:HOFFMANN LA ROCHE
    公开号:WO2014135474A1
    公开(公告)日:2014-09-12
    This application discloses compounds according to generic Formula (I): wherein all variables are defined as described herein, which inhibit BTK. The compounds disclosed herein are useful to modulate the activity of BTK and treat diseases associated with excessive BTK activity. The compounds are further useful to treat inflammatory and auto immune diseases associated with aberrant B-cell proliferation such as rheumatoid arthritis. Also disclosed are compositions containing compounds of Formula I and at least one carrier, diluent or excipient.
  • INHIBITORS OF BRUTON'S TYROSINE KINASE
    申请人:HOFFMANN-LA ROCHE INC.
    公开号:US20150376166A1
    公开(公告)日:2015-12-31
    This application discloses compounds according to generic Formula (I): wherein all variables are defined as described herein, which inhibit BTK. The compounds disclosed herein are useful to modulate the activity of BTK and treat diseases associated with excessive BTK activity. The compounds are further useful to treat inflammatory and auto immune diseases associated with aberrant B-cell proliferation such as rheumatoid arthritis. Also disclosed are compositions containing compounds of Formula I and at least one carrier, diluent or excipient.
    本申请公开了按通用式(I)定义的化合物,其中所有变量如本文所述,可抑制BTK。本文所披露的化合物有助于调节BTK的活性,治疗与过度BTK活性有关的疾病。这些化合物还有助于治疗与异常B细胞增殖有关的炎症和自身免疫性疾病,如类风湿性关节炎。还披露了含有通式I的化合物和至少一种载体、稀释剂或赋形剂的组合物。
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