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[2-(2-Methoxyphenyl)ethyl][(3-nitrophenyl)methyl]amine

中文名称
——
中文别名
——
英文名称
[2-(2-Methoxyphenyl)ethyl][(3-nitrophenyl)methyl]amine
英文别名
2-(2-methoxyphenyl)-N-[(3-nitrophenyl)methyl]ethanamine
[2-(2-Methoxyphenyl)ethyl][(3-nitrophenyl)methyl]amine化学式
CAS
——
化学式
C16H18N2O3
mdl
——
分子量
286.33
InChiKey
PBRPQLHLEAJEHK-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):
    3
  • 重原子数:
    21
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    67.1
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • SULPHONAMIDE DERIVATIVES OF BENZYLAMINE FOR THE TREATMENT OF CNS DISEASES
    申请人:ADAMED SP. Z O.O
    公开号:US20150051257A1
    公开(公告)日:2015-02-19
    Sulphonamide derivatives of benzylamine of formula (I), wherein A represents phenyl unsubstituted or substituted; or 9- or 10-membered bicyclic group, linked to —(O) x —(CH2) y — through one of its aromatic carbon atoms, consisting of benzene ring fused with -membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from the group consisting of N and O, wherein such bicyclic group is unsubstituted or substituted or with 5- or 6-membered non-aromatic heterocyclic ring having 1 or 2 O atoms, wherein heterocyclic ring is unsubstituted or substituted with one or more C 1 -C 3 -alkyls; D represents a group selected from: phenyl unsubstituted or substituted; naphthyl unsubstituted or substituted; thiophene unsubstituted or substituted; bicyclic group consisting of imidazolering fused with 5-membered non-aromatic carbocyclic ring; bicyclic group consisting of benzene ring fused with 5-membered heteroaromatic ring, having 1 or 2 heteroatoms independently selected from the group consisting of N, O and S, unsubstituted or substituted and linked to sulphonamide moiety through one of carbon atoms of benzene ring; and bicyclic group consisting of benzene ring fused with—or 6-membered non-aromatic heterocyclic ring having 1 or 2 heteroatoms independently selected from the group consisting of N and O, unsubstituted or substituted, and linked to sulphonamide moiety through one of carbon N atoms of benzene ring; R represents H or —CH 3; x is 0 or 1; y is 2 or 3; and pharmaceutically acceptable salts and solvates thereof, with the provisos that if x is 0 and y is 2, then D is naphthyl unsubstituted or substituted with one halogen atom, and if R represents —CH 3, then A is not unsubstituted or substituted phenyl. The compounds can be used in the treatment and/or prophylaxis of central nervous system disorders.
    苯甲胺的磺胺基衍生物,其化学式(I)中,A代表未取代或取代的苯基;或与—(O)x—(CH2)y—连接的9-或10-成员双环族,通过其芳香碳原子之一,由与含1或2个异原子(N和O)中独立选择的群组成的芳香环并联的苯环构成,其中此类双环族未取代或取代,或者与含1或2个O原子的5-或6-成员非芳香杂环取代或未取代,其中杂环未取代或取代为一个或多个C1-C3-烷基;D代表选自:未取代或取代的苯基;未取代或取代的萘基;未取代或取代的噻吩基;由咪唑环并联的5-成员非芳香碳环组成的双环族;由苯环并联的含1或2个异原子(N、O和S)中独立选择的群组成的5-成员杂芳环,未取代或取代,并通过苯环的一个碳原子之一与磺胺基团连接;以及由苯环并联的含1或2个异原子(N和O)中独立选择的群组成的5-或6-成员非芳香杂环取代或未取代,并通过苯环的一个碳N原子之一与磺胺基团连接;R代表H或—CH3;x为0或1;y为2或3;以及其药学上可接受的盐和溶剂合物,但如果x为0且y为2,则D为未取代或取代的萘基,且如果R代表—CH3,则A不是未取代或取代的苯基。这些化合物可用于治疗和/或预防中枢神经系统疾病。
  • [EN] SULPHONAMIDE DERIVATIVES OF BENZYLAMINE FOR THE TREATMENT OF CNS DISEASES<br/>[FR] DÉRIVÉS DE SULFONAMIDE DE LA BENZYLAMINE POUR LE TRAITEMENT DE MALADIES DU SYSTÈME NERVEUX CENTRAL (SNC)
    申请人:ADAMED SP ZOO
    公开号:WO2013140347A1
    公开(公告)日:2013-09-26
    Sulphonamide derivatives of benzylamine of formula (I), wherein A represents phenyl unsubstituted or substituted;or 9-or 10-membered bicyclic group, linked to –(O) x - (CH 2 ) y -through one of its aromatic carbon atoms,consisting of benzene ring fused with -membered heteroaromatic ring containing 1 or 2 heteroatoms independently selected from the group consisting of N and O, wherein such bicyclic group is unsubstituted or substituted or with 5-or 6-membered non-aromaticheterocyclic ring having 1 or 2 O atoms, wherein heterocyclic ring is unsubstituted or substituted with one or more C1 -C3 - alkyls; D represents a group selected from:phenyl unsubstituted or substituted; naphthyl unsubstituted or substituted;thiophene unsubstituted or substituted;bicyclic group consisting of imidazolering fused with5-membered non-aromatic carbocyclic ring; bicyclic group consisting of benzene ring fused with 5-membered heteroaromatic ring, having 1 or 2heteroatoms independently selected from the group consisting of N, O and S, unsubstituted or substituted and linked to sulphonamide moiety through one of carbon atoms of benzene ring;and bicyclic group consisting of benzene ring fused with -or 6-membered non-aromatic heterocyclic ring having 1 or 2heteroatoms independently selected from the group consisting of N and O, unsubstituted or substituted, and linked to sulphonamide moiety through one of carbon atoms of benzene ring;R represents H or –CH 3;x is 0 or 1;yis 2 or 3;and pharmaceutically acceptable salts and solvates thereof, with the provisos that if x is 0 and y is 2, then D is naphthyl unsubstituted or substituted with one halogen atom, and if R represents –CH 3, then A is not unsubstituted or substituted phenyl. The compounds can be used in the treatment and/or prophylaxis of central nervous system disorders.
    苯甲胺的磺胺基衍生物的化学式(I),其中A代表未取代或取代的苯基;或9-或10-成员的双环族,通过其中一个芳香碳原子连接到-(O) x - (CH 2 ) y -,由苯环与含有1个或2个杂原子(从N和O组成的组中独立选择)的-成员杂芳环融合而成,其中该双环族未取代或取代,或与含有1个或2个O原子的5-或6-成员非芳杂环取代,其中杂环未取代或取代为一个或多个C1 -C3 -烷基;D代表从中选择的一组:未取代或取代的苯基;未取代或取代的萘基;未取代或取代的噻吩基;由咪唑环融合而成的5-成员非芳碳环的双环族;由苯环融合而成的含有1个或2个杂原子(从N、O和S组成的组中独立选择)的5-成员杂芳环的双环族,未取代或取代,并通过苯环的一个碳原子与磺胺基团连接;以及由苯环融合而成的5-或6-成员非芳杂环的双环族,其中杂原子独立选择自N和O组成的组,未取代或取代,并通过苯环的一个碳原子与磺胺基团连接;R代表H或-CH 3;x为0或1;y为2或3;以及其药学上可接受的盐和溶剂化合物,但是如果x为0且y为2,则D为未取代或取代的萘基且带有一个卤原子,如果R代表-CH 3,则A不是未取代或取代的苯基。这些化合物可用于治疗和/或预防中枢神经系统疾病。
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