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(S)-5-甲基-7-氨基-5,7-二氢-6H-二苯并[B,D]氮杂环庚烷-6-酮盐酸盐 | 209984-55-4

中文名称
(S)-5-甲基-7-氨基-5,7-二氢-6H-二苯并[B,D]氮杂环庚烷-6-酮盐酸盐
中文别名
——
英文名称
(S,S)-7-amino-5-methyl-5H-dibenzo[b,d]azepin-6(7H)-one hydrochloride
英文别名
5-(S)-amino-7-methyl-5,7-dihydro-6H-dibenz[b,d]azepin-6-one hydrochloride;(S)-7-Amino-5-methyl-5,7-dihydro-6H-dibenzo[b,d]azepin-6-one Hydrochloride;(7S)-7-amino-5-methyl-7H-benzo[d][1]benzazepin-6-one;hydrochloride
(S)-5-甲基-7-氨基-5,7-二氢-6H-二苯并[B,D]氮杂环庚烷-6-酮盐酸盐化学式
CAS
209984-55-4
化学式
C15H14N2O*ClH
mdl
——
分子量
274.75
InChiKey
SFCMIOWXPYFQRQ-UQKRIMTDSA-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):
    2.75
  • 重原子数:
    19
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    46.3
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

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文献信息

  • Synthesis and axial chirality of an enantiopure aminodibenzazepinone
    作者:Kevin P. Cole、David Mitchell、M. Austin Carr、James R. Stout、Matthew D. Belvo
    DOI:10.1016/j.tetasy.2009.04.016
    日期:2009.6
    We propose that the inherent axial chirality contained in the dibenzazepinone works to produce an interesting chirality transfer mechanism, which accounts for the observed robustness of the stereocenter. This previously unrecognized stereochemical element exists within this specific class of molecules, and they should be drawn in a manner which displays the axial chirality.
    (S,S)-7-基-5-甲基-5 H-二苯并[ b,d ] azepin-6(7 H公开了一种盐酸盐。合成过程包括Friedel-Crafts烷基化反应以形成七元环和高效的经典拆分方法。对对映纯材料的其他研究表明,胺对消旋具有很高的抵抗力,这使我们研究了意外的稳定性。我们建议,二苯并ze庚酮中固有的轴向手性可产生有趣的手性转移机制,这说明了所观察到的立体中心的鲁棒性。这种先前无法识别的立体化学元素存在于这种特定的分子类别中,应以显示轴向手性的方式进行绘制。
  • SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USEFUL AS GAMMA-SECRETASE INHIBITORS
    申请人:F. Hoffman-la Roche AG
    公开号:EP1673347A1
    公开(公告)日:2006-06-28
  • US7166587B2
    申请人:——
    公开号:US7166587B2
    公开(公告)日:2007-01-23
  • [EN] SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USEFUL AS GAMMA-SECRETASE INHIBITORS<br/>[FR] DERIVES DE DIBENZO-AZEPINE ET DE BENZO-DIAZEPINE UTILISES EN TANT QU'INHIBITEURS DE LA GAMMA-SECRETASE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2005040126A1
    公开(公告)日:2005-05-06
    The present invention relates to compounds of the general formula (I) Wherein R1 is -(CHR’)q-aryl or -(CHR')q-heteroaryl, which are unsubstituted or mono, di- or tri-substituted by lower alkyl, lower alkoxy, CF3 or halogen, or is lower alkyl, lower alkenyl, -(CH2)n-Si(CH3)3, -(CH2)n-O-lower alkyl, -(CH2)n-S-lower alkyl, -(CH2)q-cycloalkyl, -(CH2)n-[CH(OH)]m-(CF2)p-CHqF(3-q), or is -(CH2)n-CR2-CF3, wherein the two R radicals form together with the carbon atom a cycloalkyl ring; R' is hydrogen or lower alkyl; n is 1, 2 or 3; in is 0 or 1; p is 0, 1, 2, 3, 4, 5 or 6; q is 0, 1, 2 or 3; R2 is hydrogen or lower alkyl; R3 is hydrogen, lower alkyl, -CH2CF2CF3, CH2CF3, (CH2)2CF3, CF3, CHF2, CF3, CHF2, CH2F, or is aryl, optionally mono, di or tri-substituted by halogen, or is (CH2)nNR5R6, wherein R5 and R6 are independently from each other hydrogen or lower alkyl; R4 is one of the following groups wherein R7is hydrogen, lower akl, -(CH2)n-CF3 or -(CH2)n-cycloalkyl; R8 is hydrogen, lower alkyl, -C(O)-phenyl, -C(O)-lower alkyl, -C(O)O-(CH2)n- cycloalkyl, -C(O)O-(CH2)n-lower alkyl, -C(O)NH-(CH2)n-lower alkyl or -C(O)NH­(CH2).-CyClOalkYl; R9 is hydrogen, lower alkyl, -(CH2)n-cycloalkyl or -(CH2)n-CF3; and to pharmaceutically suitable acid addition salts, optically pure enantiomers, racernates or diastereomeric mixtures thereof for the treatment of Alzheimer's disease..
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