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5-(4-methoxyphenethyl)-3-methyl-4-nitroisoxazole | 1380544-27-3

中文名称
——
中文别名
——
英文名称
5-(4-methoxyphenethyl)-3-methyl-4-nitroisoxazole
英文别名
5-[2-(4-Methoxyphenyl)ethyl]-3-methyl-4-nitro-1,2-oxazole
5-(4-methoxyphenethyl)-3-methyl-4-nitroisoxazole化学式
CAS
1380544-27-3
化学式
C13H14N2O4
mdl
——
分子量
262.265
InChiKey
NOBGRUNDMODNJZ-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):
    2.8
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    81.1
  • 氢给体数:
    0
  • 氢受体数:
    5

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

  • 作为产物:
    描述:
    5-[(E)-2-(4-Methoxy-phenyl)-vinyl]-3-methyl-4-nitro-isoxazole甲酸dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer三乙胺N-甲苯磺酰基乙二胺 作用下, 以 乙酸乙酯 为溶剂, 反应 5.0h, 以84%的产率得到5-(4-methoxyphenethyl)-3-methyl-4-nitroisoxazole
    参考文献:
    名称:
    铑配合物对共轭硝基烯烃的碳-碳双键的高度化学选择性转移氢化
    摘要:
    通过[催化的RhCl缀合的硝基烯烃化学选择性转移氢化2的Cp * ] 2 -二胺复合物(CP * =η 5 -C 5我5)使用HCOOH / ET 3 N(5:2)(TEAF)作为氢源,实现。各种硝基苯乙烯,β-甲基硝基苯乙烯和3-甲基-4-硝基-5-链烯基-异恶唑均能在短时间内以良好或极好的收率顺利还原。在反应条件下,其他官能团是惰性的。
    DOI:
    10.1016/j.tet.2012.04.028
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文献信息

  • [EN] A METHOD FOR PREPARING SULFUR-CONTAINING COMPOUNDS<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION DE COMPOSÉS CONTENANT DU SOUFRE
    申请人:ROYAL COLLEGE OF SURGEONS IE
    公开号:WO2010066450A1
    公开(公告)日:2010-06-17
    The invention provides a method for preparing sulfur-containing compounds, the method comprising reacting a donor compound comprising at least one sulfur having at least one lone pair of electrons, with an acceptor compound; wherein the reaction occurs in the presence of an amine, optionally an amine catalyst, capable of activating the sulfur having at least one lone pair of electrons; and wherein the reaction occurs via the formation of an transient intermediate species, optionally a transient intermediate species, between the amine, optionally the amine catalyst and the donor compound; and wherein the donor compound is selected from the group consisting of a sulfurous acid, a sulfenic acid and a sulfinic acid or a salt, ester or amide of a sulfurous acid, a sulfenic acid and a sulfinic acid. The invention also provides sulfur-containing compounds of the formula: wherein R is selected from: (a) 1 -(4-Nitro-phenyl)-3-oxo-3-phenyl-propane; (b) 2-(3-Methyl-4-nitro-isoxazol-5-yl)-1 -phenyl-ethane; (c) 1-(4-Methoxy-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; (d) 2-(3-Methyl-4-nitro-isoxazol-5-yl)-1-(4-nitro-phenyl)-ethane; (e) 1-(4-Fluoro-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; (f) 1 -(4-Chloro-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; and (g) 3-Oxo-cyclohexane. Finally, the invention provides use of chiral sulfur-containing compounds obtainable by the above-mentioned method or chiral sulfur-containing compounds as mentioned above for the resolution of racemic mixtures of amines.
    该发明提供了一种制备含硫化合物的方法,该方法包括将包含至少一个原子且至少一个孤对电子的给体化合物与受体化合物反应;其中,在胺的存在下进行反应,可选地,在能够激活至少一个原子具有至少一个孤对电子的胺的存在下进行反应;反应通过形成瞬态中间体物种进行,可选地,通过胺、可选地胺催化剂和给体化合物之间的瞬态中间体物种进行反应;给体化合物选自包括亚硫酸亚硫酸和亚砜酸或亚硫酸亚硫酸和亚砜酸的盐、酯或酰胺的群;该发明还提供了符合以下公式的含硫化合物:其中R选自:(a) 1-(4-硝基苯基)-3-氧代-3-苯基-丙烷;(b) 2-(3-甲基-4-硝异噁唑-5-基)-1-苯基-乙烷;(c) 1-(4-甲氧基苯基)-2-(3-甲基-4-硝异噁唑-5-基)-乙烷;(d) 2-(3-甲基-4-硝异噁唑-5-基)-1-(4-硝基苯基)-乙烷;(e) 1-(4-氟苯基)-2-(3-甲基-4-硝异噁唑-5-基)-乙烷;(f) 1-(4-氯苯基)-2-(3-甲基-4-硝异噁唑-5-基)-乙烷;和(g) 3-氧代环己烷。最后,该发明提供了通过上述方法获得的手性含硫化合物或上述提到的手性含硫化合物用于分离胺的外消旋混合物。
  • A method for preparing sulfur-containing compounds
    申请人:The Royal College of Surgeons in Ireland
    公开号:EP2196456A1
    公开(公告)日:2010-06-16
    The invention provides a method for preparing sulfur-containing compounds, the method comprising reacting a donor compound comprising at least one sulfur having at least one lone pair of electrons, with an acceptor compound; wherein the reaction occurs in the presence of a catalyst capable of activating the sulfur having at least one lone pair of electrons. The invention also provides sulfur-containing compounds of the formula: wherein R is selected from: (a) 1-(4-Nitro-phenyl)-3-oxo-3-phenyl-propane; (b) 2-(3-Methyl-4-nitro-isoxazol-5-yl)-1-phenyl-ethane; (c) 1-(4-Methoxy-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; (d) 2-(3-Methyl-4-nitro-isoxazol-5-yl)-1-(4-nitro-phenyl)-ethane; (e) 1-(4-Fluoro-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; (f) 1-(4-Chloro-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; (g) 3-Oxo-butane; (h) 2-Methyl-4-oxo-pentane-2-yl; (i) 3,4-Dihydroxy-naphthalene-2-yl; and (j) 3-Oxo-cyclohexane. Finally, the invention provides use of chiral sulfur-containing compounds obtainable by the above-mentioned method or chiral sulfur-containing compounds as mentioned above for the resolution of racemic mixtures of amines.
    本发明提供了一种制备含硫化合物的方法,该方法包括使包含至少一个具有至少一对孤对电子的的供体化合物与受体化合物反应;其中反应是在能够活化具有至少一对孤对电子的的催化剂存在下进行的。 本发明还提供了式中的含硫化合物: 其中 R 选自 (a) 1-(4-硝基苯基)-3-氧代-3-苯基-丙烷; (b) 2-(3-甲基-4-硝基异恶唑-5-基)-1-苯基乙烷; (c) 1-(4-甲氧基苯基)-2-(3-甲基-4-硝基异恶唑-5-基)-乙烷 (d) 2-(3-甲基-4-硝基-异恶唑-5-基)-1-(4-硝基苯基)-乙烷 (e) 1-(4-氟苯基)-2-(3-甲基-4-硝基-异恶唑-5-基)乙烷 (f) 1-(4-氯苯基)-2-(3-甲基-4-硝基异恶唑-5-基)乙烷; (g) 3-氧代丁烷 (h) 2-Methyl-4-oxo-pentane-2-yl; (i) 3,4-二羟基-2-基;以及 (j) 3-氧代环己烷。 最后,本发明提供了可通过上述方法获得的手性含硫化合物或上述手性含硫化合物在胺外消旋混合物解析中的用途。
  • A METHOD FOR PREPARING SULFUR-CONTAINING COMPOUNDS
    申请人:The Royal College of Surgeons in Ireland
    公开号:EP2376444A1
    公开(公告)日:2011-10-19
  • Method for Preparing Sulfur-Containing Compounds
    申请人:Mauro Adamo
    公开号:US20120029197A1
    公开(公告)日:2012-02-02
    The invention provides a method for preparing sulfur-containing compounds, the method comprising reacting a donor compound comprising at least one sulfur having at least one lone pair of electrons, with an acceptor compound; wherein the reaction occurs in the presence of an amine, optionally an amine catalyst, capable of activating the sulfur having at least one lone pair of electrons; and wherein the reaction occurs via the formation of an transient intermediate species, optionally a transient intermediate species, between the amine, optionally the amine catalyst and the donor compound; and wherein the donor compound is selected from the group consisting of a sulfurous acid, a sulfenic acid and a sulfinic acid or a salt, ester or amide of a sulfurous acid, a sulfenic acid and a sulfinic acid. The invention also provides sulfur-containing compounds of the formula: wherein R is selected from: (a) 1-(4-Nitro-phenyl)-3-oxo-3-phenyl-propane; (b) 2-(3-Methyl-4-nitro-isoxazol-5-yl)-1-phenyl-ethane; (c) 1-(4-Methoxy-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; (d) 2-(3-Methyl-4-nitro-isoxazol-5-yl)-1-(4-nitro-phenyl)-ethane; (e) 1-(4-Fluoro-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; (f) 1-(4-Chloro-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane; and (g) 3-Oxo-cyclohexane. Finally, the invention provides use of chiral sulfur-containing compounds obtainable by the above-mentioned method or chiral sulfur-containing compounds as mentioned above for the resolution of racemic mixtures of amines.
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