benzyl (S)-1-(N-allyl-4-methylbenzenesulfonamido)-3,3-dimethylbutan-2-ylcarbamate | 1007121-83-6

• 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: benzyl (S)-1-(N-allyl-4-methylbenzenesulfonamido)-3,3-dimethylbutan-2-ylcarbamate
• 英文别名: benzyl N-[(2S)-3,3-dimethyl-1-[(4-methylphenyl)sulfonyl-prop-2-enylamino]butan-2-yl]carbamate
• CAS: 1007121-83-6
• 化学式: C₂₄H₃₂N₂O₄S
• 分子量: 444.595
• InChiKey: GLHYOZCJTYTCON-JOCHJYFZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  31
• 可旋转键数：
  11
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  84.1
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  (S)-3-(benzyloxycarbonyl)-4-tert-butyl-[1,2,3]oxathiazolidine 2,2-dioxide 、 N-烯丙基对甲苯磺酰胺 在 氢氧化钾 、 盐酸 作用下， 以 乙腈 、 乙酸乙酯 为溶剂， 以89%的产率得到benzyl (S)-1-(N-allyl-4-methylbenzenesulfonamido)-3,3-dimethylbutan-2-ylcarbamate
  参考文献：
  名称：

  Synthesis of 2,6-Disubstituted Piperazines by a Diastereoselective Palladium-Catalyzed Hydroamination Reaction

  摘要：

  A highly diastereoselective intramolecular hydroamination is the key step in a modular synthesis of 2,6-disubstituted piperazines. The requisite hydroamination substrates were prepared in excellent yields by nucleophilic displacement of cyclic sulfamidates derived from amino acids. A variety of alkyl and aryl substituents at the 2-position were tolerated. The stereochemistry of the piperazines was determined to be trans by X-ray crystallography, which also showed the preferred conformation of the 2,6-disubstituted piperazine to be a twist-boat due to A(1,3) strain.

  DOI：

  10.1021/ol702891p

文献信息

• Synthesis of 2,6-Disubstituted Piperazines by a Diastereoselective Palladium-Catalyzed Hydroamination Reaction
  作者：Brian M. Cochran、Forrest E. Michael

  DOI：10.1021/ol702891p

  日期：2008.1.1

  A highly diastereoselective intramolecular hydroamination is the key step in a modular synthesis of 2,6-disubstituted piperazines. The requisite hydroamination substrates were prepared in excellent yields by nucleophilic displacement of cyclic sulfamidates derived from amino acids. A variety of alkyl and aryl substituents at the 2-position were tolerated. The stereochemistry of the piperazines was determined to be trans by X-ray crystallography, which also showed the preferred conformation of the 2,6-disubstituted piperazine to be a twist-boat due to A(1,3) strain.