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(Z)-11-(3-dimethylaminopropylidene)-6,11-dihydrodibenz[b,e] oxepin-2-acetic acid ethyl ester | 113806-03-4

中文名称
——
中文别名
——
英文名称
(Z)-11-(3-dimethylaminopropylidene)-6,11-dihydrodibenz[b,e] oxepin-2-acetic acid ethyl ester
英文别名
Olopatadine Ethyl Ester;ethyl 2-[(11Z)-11-[3-(dimethylamino)propylidene]-6H-benzo[c][1]benzoxepin-2-yl]acetate
(Z)-11-(3-dimethylaminopropylidene)-6,11-dihydrodibenz[b,e] oxepin-2-acetic acid ethyl ester化学式
CAS
113806-03-4
化学式
C23H27NO3
mdl
——
分子量
365.472
InChiKey
CTPMOZRLWGCTTL-JMIUGGIZSA-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:
    499.0±45.0 °C(Predicted)
  • 密度:
    1.148±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    27
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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

点击查看最新优质反应信息

文献信息

  • PROCESS FOR OBTAINING OLOPATADINE AND INTERMEDIATES
    申请人:Silva Guisasola Luis Octavio
    公开号:US20120004426A1
    公开(公告)日:2012-01-05
    Olopatadine can be obtained by means of a process comprising hydrolysis of a compound of general formula (II), wherein Y is OR 1 , wherein R 1 is C 1 -C 7 alkyl, C 3 -C 7 cycloalkyl, aryl, arylalkyl, or heterocycle; or NR 2 R 3 , wherein R 2 and R 3 , independently from each other, are C 1 -C 7 alkyl, aryl, arylalkyl, or R 2 and R 3 together with the nitrogen atom to which they are bound form a heterocycle of 3 to 7 members, obtained by means of a process comprising reacting the corresponding ester or amide of 6,11-dihydro-11-oxodibenz[b,e]oxepin-2-acetic acid with a suitable Wittig reagent, in the presence of a base in a reaction medium comprising an organic solvent.
    Olopatadine可以通过以下过程获得:水解通式(II)的化合物,其中Y为OR1,其中R1为C1-C7烷基,C3-C7环烷基,芳基,芳基烷基或杂环;或者NR2R3,其中R2和R3分别独立地为C1-C7烷基,芳基,芳基烷基,或者R2和R3与它们所结合的氮原子形成3至7个成员的杂环,所述过程包括在有机溶剂的反应介质中,在碱的存在下,通过反应相应的6,11-二氢-11-氧代二苯[b,e]氧杂环-2-乙酸酯或酰胺与适当的Wittig试剂反应而得到。
  • USE OF CONNECTIVE TISSUE MAST CELL STABILIZERS TO FACILITATE OCULAR SURFACE RE-EPITHELIZATION AND WOUND REPAIR
    申请人:Yanni John M.
    公开号:US20080139531A1
    公开(公告)日:2008-06-12
    Disclosed are methods of treating a wound in a subject that involve administering to the subject a pharmaceutically effective amount of a composition that includes one or more human connective tissue mast cell stabilizers, wherein administration of the composition results in treatment of the wound. In particular embodiments, the wound is an ophthalmic or dermal wound, such as a corneal epithelial defect, a conjunctival wound, or dermal abrasion. Administration, for example, may be by topical application of the composition to the ocular surface or skin. Exemplary mast cell stabilizers include olopatadine, variants of olopatadine, alcaftidine, derivatives of alcaftidine, dihydropyridines, and spleen tyrosine kinase inhibitors.
  • US9000195B2
    申请人:——
    公开号:US9000195B2
    公开(公告)日:2015-04-07
  • Process for obtaining olopatadine and intermediates
    申请人:Crystal Pharma, S.A.U.
    公开号:EP2145882B1
    公开(公告)日:2013-08-21
  • [EN] PROCESS FOR OBTAINING OLOPATADINE AND INTERMEDIATES<br/>[FR] PROCÉDÉ D'OBTENTION D'OLOPATADINE ET DE SES INTERMÉDIAIRES
    申请人:RAGACTIVES S L U
    公开号:WO2010007056A1
    公开(公告)日:2010-01-21
    Olopatadine can be obtained by means of a process comprising hydrolysis of a compound of general formula (II), wherein Y is OR1, wherein R1 is C1-C7 alkyl, C3-C7 cycloalkyl, aryl, arylalkyl, or heterocycle; or NR2R3, wherein R2 and R3, independently from each other, are C1-C7 alkyl, aryl, arylalkyl, or R2 and R3 together with the nitrogen atom to which they are bound form a heterocycle of 3 to 7 members, obtained by means of a process comprising reacting the corresponding ester or amide of 6,11-dihydro-11- oxodibenz[b,e]oxepin-2-acetic acid with a suitable Wittig reagent, in the presence of a base in a reaction medium comprising an organic solvent.
    Olopatadine可以通过一种过程获得,包括对通式(II)的化合物进行水解,其中Y为OR1,其中R1为C1-C7烷基,C3-C7环烷基,芳香族,芳香族烷基或杂环;或NR2R3,其中R2和R3独立地为C1-C7烷基,芳香族,芳香族烷基,或R2和R3与它们所结合的氮原子形成3至7个成员的杂环,通过在有机溶剂反应介质中,在碱存在下,与适当的Wittig试剂反应,获得6,11-二氢-11-氧代二苯[b,e]氧杂环-2-乙酸相应的酯或酰胺。
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