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Methyl-cis-3-hydroxy-cis-4-bromocyclohexan-1-carboxylat | 643070-22-8

中文名称
——
中文别名
——
英文名称
Methyl-cis-3-hydroxy-cis-4-bromocyclohexan-1-carboxylat
英文别名
(1R,3R,4S)-4-bromo-3-hydroxy-cyclohexanecarboxylic acid methyl ester;methyl (1R,3R,4S)-4-bromo-3-hydroxycyclohexane-1-carboxylate
Methyl-cis-3-hydroxy-cis-4-bromocyclohexan-1-carboxylat化学式
CAS
643070-22-8
化学式
C8H13BrO3
mdl
——
分子量
237.093
InChiKey
SQOUCOUCDZRJKH-DSYKOEDSSA-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):
    1.1
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    Methyl-cis-3-hydroxy-cis-4-bromocyclohexan-1-carboxylat 在 sodium azide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 8.0h, 生成 (1R,3R,4R)-4-azido-3-hydroxy-cyclohexanecarboxylic acid methyl ester
    参考文献:
    名称:
    Novel cyclohexyl-amides as potent antibacterials targeting bacterial type IIA topoisomerases
    摘要:
    As part of our wider efforts to exploit novel mode of action antibacterials, we have discovered a series of cyclohexyl-amide compounds that has good Gram positive and Gram negative potency. The mechanism of action is via inhibition of bacterial topoisomerases II and IV. We have investigated various subunits in this series and report advanced studies on compound 7 which demonstrates good PK and in vivo efficacy properties. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.09.114
  • 作为产物:
    参考文献:
    名称:
    Novel cyclohexyl-amides as potent antibacterials targeting bacterial type IIA topoisomerases
    摘要:
    As part of our wider efforts to exploit novel mode of action antibacterials, we have discovered a series of cyclohexyl-amide compounds that has good Gram positive and Gram negative potency. The mechanism of action is via inhibition of bacterial topoisomerases II and IV. We have investigated various subunits in this series and report advanced studies on compound 7 which demonstrates good PK and in vivo efficacy properties. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.09.114
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文献信息

  • [EN] COMPOUNDS<br/>[FR] COMPOSÉS
    申请人:GLAXO GROUP LTD
    公开号:WO2004002992A1
    公开(公告)日:2004-01-08
    Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man. A compound of formula (I) or a pharmaceutically acceptable derivative thereof: (I) RA is an optionally substituted bicyclic carbocyclic or heterocyclic ring system of structure: containing 0-3 heteroatmoms in each ring in which: at least one of the rings (x) and (y) is aromatic; one of Z4 and Z5 is C or N and the other is C; Z3 is N, NR13, O, S(O)x, CO, CR1 or CR1R1a; Z1 and Z2 are indendently a 2 or 3 atom linker group each atom of which is independently selected from N, NR13, O, S(O)x, CO, CR1, and CR1R1a; such that each ring is independently substituted with 0-3 groups R1 and/or R1a. R4 is a group -CH2-R51in which R51 is selected from: (C4-8) alkyl; hydroxy (C4-8) alkyl; (C1-4)alkoxy (C4-8)alkyl; (C1-4) alkanoyloxy (C4-8) alkyl; (C3-8)cycloalkyl (C 4-8)alkyl;hydroxy-, (C1-6) alkoxy- or (C1-6) alkanoyloxy-(C3-8)cycloalkyl (C4-8)alkyl; cyano(C4-8)alkyl; (C4-8)alkenyl; (C4-8)alkynyl; tetrahydrofuryl; mono- or di-(C1-6)alkylamino (C4-8)alkyl; acylamino (C4-8)alkyl; C(1-6)alkyl- or acyl-aminocarbonyl (C4-8) alkyl; mono- or di- (C1-6)alkylamino(hydroxy) (C4-8)alkyl; or R4 is a group-U-R52 where R52 is an optionally substituted bicyclic carbocyclic or heterocyclic ring system (A): containing up to four heteroatoms in each ring in which at least one of rings (a) and (b) is aromatic; X1 is C or N when part of an aromatic ring or CR14 when part of a non-aromatic ring.
    环己烷和环己烯衍生物及其在治疗哺乳动物,特别是人类细菌感染方法中有用的药用可接受衍生物。一种公式(I)的化合物或其药用可接受的衍生物:(I) RA是一个可选地取代的双环碳环或杂环环系结构:包含每个环中的0-3个杂原子,其中:至少一个环(x)和(y)是芳香的;Z4和Z5中的一个为C或N,另一个为C;Z3是N,NR13,O,S(O)x,CO,CR1或CR1R1a;Z1和Z2是独立选择的2或3原子连接基团,每个原子独立地选自N,NR13,O,S(O)x,CO,CR1,和CR1R1a;使得每个环独立地用0-3个组R1和/或R1a取代。R4是一个组-CH2-R51,其中R51选自:(C4-8)烷基;羟基(C4-8)烷基;(C1-4)烷氧基(C4-8)烷基;(C1-4)烷酰氧基(C4-8)烷基;(C3-8)环烷基(C4-8)烷基;羟基-,(C1-6)烷氧基-或(C1-6)烷酰氧基-(C3-8)环烷基(C4-8)烷基;氰基(C4-8)烷基;(C4-8)烯基;(C4-8)炔基;四氢呋喃基;单或二-(C1-6)烷基氨基(C4-8)烷基;酰氨基(C4-8)烷基;C(1-6)烷基-或酰基-氨基甲酰基(C4-8)烷基;单或二-(C1-6)烷基氨基(羟基)(C4-8)烷基;或R4是一个组-U-R52,其中R52是一个可选地取代的双环碳环或杂环环系(A):每个环中含最多四个杂原子,其中至少一个环(a)和(b)是芳香的;X1是C或N当其作为芳香环的一部分,或CR14当其作为非芳香环的一部分。
  • Compounds
    申请人:Axten Michael Jeffrey
    公开号:US20060189604A1
    公开(公告)日:2006-08-24
    Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man.
    环己烷和环己烯衍生物及其药学上可接受的衍生物在哺乳动物中,特别是人类中用于治疗细菌感染的方法中具有用途。
  • Antimicrobial Compounds
    申请人:Axten Jeffrey Michael
    公开号:US20100081650A1
    公开(公告)日:2010-04-01
    Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man.
    环己烷和环己烯衍生物及其药学上可接受的衍生物,可用于治疗哺乳动物,特别是人类的细菌感染方法。
  • Antibacterial compounds
    申请人:Glaxo Group Limited
    公开号:US07622481B2
    公开(公告)日:2009-11-24
    Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man.
    环己烷和环己烯衍生物及其药学上可接受的衍生物在哺乳动物,特别是人类的细菌感染治疗方法中有用。
  • Miyashita Kazuyuki, Tanaka Akira, Mizuno Hiroaki, Tanaka Masahiro, Iwata +, J. Chem. Soc. Perkin Trans. 1, (1994) N 7, S 847- 851
    作者:Miyashita Kazuyuki, Tanaka Akira, Mizuno Hiroaki, Tanaka Masahiro, Iwata +
    DOI:——
    日期:——
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