N-[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]-4-methylbenzenesulfonamide

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]-4-methylbenzenesulfonamide
• 英文别名: N-[(1S,2R)-1-hydroxy-1-phenylpropan-2-yl]-4-methylbenzenesulfonamide
• 化学式: C₁₆H₁₉NO₃S
• 分子量: 305.398
• InChiKey: CRZOLKWUJOHXED-CZUORRHYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  74.8
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  N-[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]-4-methylbenzenesulfonamide 在 氯化亚砜 、 N,N-二甲基甲酰胺 作用下， 以 二氯甲烷 、 氯仿 、 乙腈 为溶剂， 反应 2.0h， 生成 (1S,2R)-(-)-1-phenyl-1-(1-benzylamino)-2-(tosylamino)propane
  参考文献：
  名称：

  Remarkable enantioselective α-amination in 1-phenyl-2-(n-alkylamino)-1-propanol

  摘要：

  Abstract(1R,2R)‐1‐Phenyl‐1‐alkyl/arylamino‐2‐(N‐alkylamino)propane hydrochloride salts have been synthesized with high degree of enantiomeric purity from (1S,2R)‐(+)‐1‐phenyl‐2‐(N‐alkylamino)‐1‐propanol through the corresponding chloro derivatives. This reaction sequence involves three inversions with overall inversion of configuration at C‐1. Chirality, 2012. © 2012 Wiley Periodicals, Inc.

  DOI：

  10.1002/chir.21996
• 作为产物：
  描述：

  (1R,2R)-1-phenyl-2-(1-piperidinyl)-1-chloropropane hydrochloride 在 水 、 三乙胺 作用下， 以 四氢呋喃 为溶剂， 生成 N-[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]-4-methylbenzenesulfonamide
  参考文献：
  名称：

  Remarkable enantioselective α-amination in 1-phenyl-2-(n-alkylamino)-1-propanol

  摘要：

  Abstract(1R,2R)‐1‐Phenyl‐1‐alkyl/arylamino‐2‐(N‐alkylamino)propane hydrochloride salts have been synthesized with high degree of enantiomeric purity from (1S,2R)‐(+)‐1‐phenyl‐2‐(N‐alkylamino)‐1‐propanol through the corresponding chloro derivatives. This reaction sequence involves three inversions with overall inversion of configuration at C‐1. Chirality, 2012. © 2012 Wiley Periodicals, Inc.

  DOI：

  10.1002/chir.21996

文献信息

• Rhodium complex with unsymmetrical vicinal diamine ligand: excellent catalyst for asymmetric transfer hydrogenation of ketones
  作者：Sudhindra H. Deshpande、Vaishali S. Shende、Savita K. Shingote、Debamitra Chakravarty、Vedavati G. Puranik、Raghunath V. Chaudhari、Ashutosh A. Kelkar

  DOI：10.1039/c5ra08220j

  日期：——

  investigated. The reaction mixture is homogeneous in methanol unlike in water, where substrate and product are insoluble in water and form separate phase, sodium formate being soluble in water. The activity and enantioselectivity obtained for ATH of ketones using [Rh(Cp*)Cl2]2 and unsymmetrical vicinal diamine ligand as catalyst was comparable with the C2 symmetric benchmark ligands like TsDPEN ((1R,2R)-N-(p-tolylsulfonyl)-1

  从便宜的起始原料如去氧麻黄碱合成了新的不对称邻位二胺配体，其胺和磺酰胺基团的区域和立体位置发生系统性变化。已经研究了使用过渡金属配合物和以甲酸钠为氢源的单甲苯磺酸化不对称邻位二胺配体的新衍生物在水中和甲醇中对芳族烷基酮的催化不对称转移加氢（ATH）。以优异的对映选择性（> 95％ee）和[Rh（Cp *）Cl 2 ] 2和配体4转化酮（> 95％）获得手性仲醇作为催化剂。与使用水作为溶剂相比，发现使用甲醇作为酮（以甲酸钠为氢源）进行ATH的溶剂时，对映选择性略高，并且发现与所有研究的酮均相符。与在水中不同，反应混合物在甲醇中是均相的，在水中，底物和产物不溶于水并形成分离的相，而甲酸钠则溶于水。的活性和对映选择性使用酮为ATH获得的[Rh（CP *）氯2 ] 2和不对称连位二胺配体作为催化剂是与可比较的C ^ 2点对称基准的配体等TsDPEN（（1 - [R，2 - [R ） - ñ - （p-甲苯基磺酰基）-1
• Enantioselective synthesis of optically active homoallylamines by nucleophilic addition of chirally modified allylboranes to N-silylimines
  作者：Shinichi Itsuno、Katsuhiro Watanabe、Takeshi Matsumoto、Shizue Kuroda、Ayako Yokoi、Ashraf El-Shehawy

  DOI：10.1039/a902635e

  日期：——

  Enantioselectivity in the allylboration of N-silylimines with a variety of chirally modified allylboron reagents has been examined. Optically active N-sulfonylamino alcohols (16, 17 and 19) derived from D-camphor and norephedrine were found to be efficient chiral ligands for the allylboration reagent. These reagents smoothly reacted with N-silylimines to give the corresponding homoallylic amines in

  已经研究了N-甲硅烷基丙胺与多种手性改性的烯丙基硼试剂在烯丙基硼化中的对映选择性。发现衍生自D-樟脑和去氧麻黄碱的旋光性N-磺酰基氨基醇（16、17和19）是烯丙基硼化试剂的有效手性配体。这些试剂与N-甲硅烷基亚胺平滑反应，以高达96％ee的高对映体选择性得到相应的均烯丙基胺。
• Access to Optically Pure Benzosultams by Superelectrophilic Activation
  作者：Bastien Michelet、Ugo Castelli、Emeline Appert、Maude Boucher、Kassandra Vitse、Jérôme Marrot、Jérôme Guillard、Agnès Martin-Mingot、Sébastien Thibaudeau

  DOI：10.1021/acs.orglett.0c01301

  日期：2020.7.2

  N-(arenesulfonyl)-aminoalcohols derived from readily available ephedrines or amino acids undergo an intramolecular Friedel–Crafts reaction to afford enantiopure benzosultams bearing two adjacent stereocenters in high yields with fully controlled diastereoselectivity. Low-temperature NMR spectroscopy demonstrated the crucial role played by the conformationally restricted chiral dicationic intermediates.

  通过超强酸活化，源自易于获得的麻黄碱或氨基酸的N-（芳烃磺酰基）-氨基醇会经历分子内Friedel-Crafts反应，以高产率得到对映体纯的苯并阿苏二胺，并具有完全受控的非对映选择性，并带有两个相邻的立体中心。低温NMR光谱表明，构象受限的手性双效中间体具有重要作用。
• Reagent-switch controlled metal-free intermolecular geminal diamination and aminooxygenation of vinylarenes
  作者：Pandur Venkatesan Balaji、Srinivasan Chandrasekaran

  DOI：10.1016/j.tet.2016.01.005

  日期：2016.2

  using hypervalent iodine reagent. A new m-CPBA mediated geminal aminooxygenation is also reported. A novel reagent-switch for the control of migrating group by controlling the two independent geminal addition paths is developed. Deuterium labelling studies and the control studies have provided unambiguous evidences for the phenyl migration and hydride migration in the oxidative geminal difunctionalization

  我们在这里报告了使用高价碘试剂进行芳基化的第一个一般方法，以及乙烯基芳烃的无分子间金属化，芳基化的氨基氧化。还报道了新的由m -CPBA介导的双链氨基氧化。开发了一种通过控制两个独立的双链加成路径来控制迁移基团的新型试剂开关。氘标记研究和对照研究提供了明确的证据，证明苯酚和氢化物迁移分别通过半频哪醇重排由PhI（OCOCF 3）2和m -CPBA介导的氧化双子双官能化过程中。
• Stereoselective geminal difunctionalization of vinyl arenes mediated by the bromonium ion
  作者：Pandur Venkatesan Balaji、Srinivasan Chandrasekaran

  DOI：10.1039/c3cc46003g

  日期：——

  An anti-Markovnikov geminal oxyamination of styrenyl alkenes in an intermolecular fashion using the umpolung strategy mediated by the bromonium ion is reported. Isotope labeling studies confirm the migration of the phenyl group in the semipinacol rearrangement.

  报道了使用溴离子介导的聚对苯二酚策略以分子间方式对苯乙烯基烯烃进行抗马尔科夫尼科夫双键氧化胺化反应。同位素标记研究证实了在频哪醇重排中苯基的迁移。