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(Z)-4,4-difluoro-5-{2-[4-(hydroxyimino)piperidino]-2-oxo-ethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine | 213023-24-6

中文名称
——
中文别名
——
英文名称
(Z)-4,4-difluoro-5-{2-[4-(hydroxyimino)piperidino]-2-oxo-ethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine
英文别名
(2Z)-2-[4,4-difluoro-1-(4-methyl-2-phenyl-1,3-thiazole-5-carbonyl)-2,3-dihydro-1-benzazepin-5-ylidene]-1-(4-hydroxyiminopiperidin-1-yl)ethanone
(Z)-4,4-difluoro-5-{2-[4-(hydroxyimino)piperidino]-2-oxo-ethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine化学式
CAS
213023-24-6
化学式
C28H26F2N4O3S
mdl
——
分子量
536.602
InChiKey
IIEQEWPRLOULJL-XLNRJJMWSA-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):
    4.2
  • 重原子数:
    38
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    114
  • 氢给体数:
    1
  • 氢受体数:
    8

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

  • 作为反应物:
    描述:
    (Z)-4,4-difluoro-5-{2-[4-(hydroxyimino)piperidino]-2-oxo-ethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine乙酸酐乙酸乙酯盐酸magnesium sulfate 、 silica gel 、 氯仿 作用下, 以 吡啶 为溶剂, 反应 8.0h, 以to give 36 mg of (Z)-4,4-difluoro-5-{2-[4-(acetoxyimino)piperidino]-2-oxoethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine as a colorless solid的产率得到(Z)-4,4-difluoro-5-{2-[4-(acetoxyimino)piperidino]-2-oxoethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine
    参考文献:
    名称:
    4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine derivatives and drug compositions containing them
    摘要:
    4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐以及含有4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐和药学上可接受的载体的制药组合物。这些化合物的化学结构特征是在邻近苯并氮杂环碳原子上带有二氟基,该碳原子被甲基亚甲基基取代。含有这些化合物的制药组合物特别适用于催产素拮抗剂,并有效地抑制威胁性早产或流产和剖腹产,并作为治疗痛经和其他类似情况的药物。
    公开号:
    US06340678B1
  • 作为产物:
    描述:
    (Z)-1-{[4,4-difluoro-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepin-5-ylidene]acetyl}piperidin-4-one盐酸羟胺三乙胺 在 silica gel 、 chloroform methanol乙醚 作用下, 以 二氯甲烷甲醇 为溶剂, 反应 22.0h, 以to give 61 mg of (Z)-4,4-difluoro-5-{2-[4-(hydroxyimino)piperidino]-2-oxo-ethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine as a colorless powder的产率得到(Z)-4,4-difluoro-5-{2-[4-(hydroxyimino)piperidino]-2-oxo-ethylidene}-1-(4-methyl-2-phenylthiazole-5-carbonyl)-2,3,4,5-tetrahydro-1H-1-benzoazepine
    参考文献:
    名称:
    4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine derivatives and drug compositions containing them
    摘要:
    4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐以及含有4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐和药学上可接受的载体的制药组合物。这些化合物的化学结构特征是在邻近苯并氮杂环碳原子上带有二氟基,该碳原子被甲基亚甲基基取代。含有这些化合物的制药组合物特别适用于催产素拮抗剂,并有效地抑制威胁性早产或流产和剖腹产,并作为治疗痛经和其他类似情况的药物。
    公开号:
    US06340678B1
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文献信息

  • 4,4-DIFLUORO-2,3,4,5-TETRAHYDRO-1H-1-BENZAZEPINE DERIVATIVES AND DRUG COMPOSITIONS CONTAINING THEM
    申请人:YAMANOUCHI PHARMACEUTICAL CO. LTD.
    公开号:EP0987264A1
    公开(公告)日:2000-03-22
    4,4-Difluoro-2,3,4,5-tetrahydro-1H-1-benzazepine derivatives represented by the following formula (I) or salts thereof: (wherein each of the symbols has the following meaning: ring A: a 5-membered heteroarylene group; ring B: an optionally substituted aryl group or a 5- to 6-membered heteroaryl group; D: a carbonyl group or a lower alkylene group; R1: a group represented by formula, NR3R4, an -O-lower alkyl group, or OH; R2: an optionally halogen atom-substituted lower alkyl group, an -O-lower alkyl group, an -S-lower alkyl group, or a -CO-lower alkyl group; R3, R4: same or different and each is 1) a hydrogen atom, 2) a lower alkyl group (the lower alkyl group may be substituted with OH, an optionally protected amino group, an optionally protected mono-lower alkylamino group, a di-lower alkylamino group, an optionally lower alkyl group-substituted 5- to 7-membered saturated heterocyclic group, a 5- to 6-membered heteroaryl group, or an aryl group), 3) a cycloalkyl group, 4) an optionally lower alkyl group-substituted 5- to 7-membered saturated heterocyclic group, 5) a 5- to 6-membered heteroaryl group, 6) an aryl group, or 7) an optionally substituted 5- to 7-membered nitrogen-containing heterocyclic group formed by integration of the formula, NR3R4 (the 5- to 7-membered nitrogen-containing heterocyclic group may be fused with a benzene ring or with a 5- to 6-membered heteroaryl group); (in the 5- to 7-membered saturated heterocyclic group, the 5-to 7-membered nitrogen-containing heterocyclic group and the 5- to 6-membered heteroaryl group in the above 2), 4), 5) and 7), a group having a cyclic secondary amine may be one wherein the amine is protected); and n: 0, 1 or 2.) The compounds of the present invention exhibit the oxytocin antagonism and are effective in inhibiting threatened premature birth or abortion, or precesarean birth and useful as remedies for dysmenorrhea and so.
    下式(I)代表的 4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂卓衍生物或其盐类: (其中各符号含义如下: 环 A:5 元杂芳基; 环 B:任选取代的芳基或 5 至 6 元杂芳基; D:羰基或低级烯基; R1:由式 NR3R4、-O-低级烷基或 OH 代表的基团; R2:由卤原子取代的低级烷基、-O-低级烷基、-S-低级烷基或-CO-低级烷基; R3、R4:相同或不同,且各自为 1) 一个氢原子 2)低级烷基(低级烷基可被 OH、任选保护的氨基、任选保护的单低级烷基氨基、二低级烷基氨基、任选被低级烷基取代的 5-7 元饱和杂环基、5-6 元杂芳基或芳基取代)、 3) 环烷基、 4) 一个任选被低级烷基取代的 5 至 7 元饱和杂环基团、 5) 5 至 6 元杂芳基、 6) 芳基,或 7) 由式 NR3R4 整合而成的任选取代的 5 至 7 元含氮杂环基团(5 至 7 元含氮杂环基团可与苯环或 5 至 6 元杂芳基融合);(在上述 2)、4)、5)和 7)中的 5 至 7 元饱和杂环基团、5 至 7 元含氮杂环基团和 5 至 6 元杂芳基团中,具有环状仲胺的基团可以是胺被保护的基团);以及 n:0、1 或 2)。 本发明的化合物表现出催产素拮抗作用,可有效抑制威胁性早产或流产,或剖腹产,并可作为治疗痛经等的药物。
  • US6340678B1
    申请人:——
    公开号:US6340678B1
    公开(公告)日:2002-01-22
  • 4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine derivatives and drug compositions containing them
    申请人:Yamanouchi Pharmaceutical Co., Ltd.
    公开号:US06340678B1
    公开(公告)日:2002-01-22
    4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine compounds or salts thereof and pharmaceutical compositions containing 4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine compounds, or salts thereof, and a pharmaceutically acceptable carrier. The chemical structure of these compounds is characterized by a difluoro group on a ring carbon atom adjacent to an azepine ring carbon atom substituted with a methylidene group. Pharmaceutical compositions containing these compounds are particularly useful as oxytocin antagonists and are effective in inhibiting threatened premature birth or abortion and precesarean birth, and are effective as a remedy for dysmenorrhea and other such conditions.
    4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐以及含有4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐和药学上可接受的载体的制药组合物。这些化合物的化学结构特征是在邻近苯并氮杂环碳原子上带有二氟基,该碳原子被甲基亚甲基基取代。含有这些化合物的制药组合物特别适用于催产素拮抗剂,并有效地抑制威胁性早产或流产和剖腹产,并作为治疗痛经和其他类似情况的药物。
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