(5S)-2-hydroxy-N'-(4-methoxy-2,3,6-trimethylphenyl)sulfonyl-5-(2-phenylmethoxyethyl)pyrrolidine-1-carboximidamide | 316831-30-8

• 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: (5S)-2-hydroxy-N'-(4-methoxy-2,3,6-trimethylphenyl)sulfonyl-5-(2-phenylmethoxyethyl)pyrrolidine-1-carboximidamide
• CAS: 316831-30-8
• 化学式: C₂₄H₃₃N₃O₅S
• 分子量: 475.609
• InChiKey: SHOCGZSZJVRLDC-AIBWNMTMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  33
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  123
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  乙酰丙酮苄酯 、 (5S)-2-hydroxy-N'-(4-methoxy-2,3,6-trimethylphenyl)sulfonyl-5-(2-phenylmethoxyethyl)pyrrolidine-1-carboximidamide 在 PPE 作用下， 以 二氯甲烷 为溶剂， 反应 48.0h， 以61%的产率得到(4aS,7S)-7-(2-benzyloxyethyl)-1-(4-methoxy-2,3,6-trimethylbenzenesulfonylimino)-3-methyl-1,2,4a,5,6,7-hexahydropyrrolo<1,2-c>pyrimidine-4-carboxylic acid benzyl ester
  参考文献：
  名称：

  Tuning Stereoselection in Tethered Biginelli Condensations. Synthesis of cis- or trans-1-Oxo- and 1-Iminohexahydropyrrolo[1,2-c]pyrimidines

  摘要：

  Stereoselection in tethered Biginelli condensations can be tuned to give either the cia or trans stereoisomer of 1-oxohexahydropyrrolo[1,2-c]pyrimidine and 1-iminohexahydropyrrolo[1,2-c]pyrimidine products (see eq 1). With substrates having urea and N-sulfonylguanidine functionality (Schemes 2 and 4), cis stereoselection (4-7:1) is observed when the condensation is accomplished under Knoevenagel conditions, while trans stereoselection (4-20:1) is observed when the condensation is carried out in the presence of polyphosphate ester (PPE). Under both conditions, steroselectivity is highest in the N-sulfonylguanidine series. With substrates bearing a basic guanidine unit, the trans product is formed exclusively under Knoevenagel conditions (Scheme 3).

  DOI：

  10.1021/jo981972g
• 作为产物：
  描述：

  (R)-3-羟基-7-甲基-6-辛烯酸甲酯 在 lead(IV) acetate 、 四氧化锇 、 lithium aluminium tetrahydride 、 N-甲基吲哚酮 、 三(2-氯乙基)胺 、 氨 、 sodium hydride 、 silver nitrate 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 吡啶 、 乙醚 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 、 甲苯 、 乙腈 、 叔丁醇 、 苯 为溶剂， 反应 23.0h， 生成 (5S)-2-hydroxy-N'-(4-methoxy-2,3,6-trimethylphenyl)sulfonyl-5-(2-phenylmethoxyethyl)pyrrolidine-1-carboximidamide
  参考文献：
  名称：

  Tuning Stereoselection in Tethered Biginelli Condensations. Synthesis of cis- or trans-1-Oxo- and 1-Iminohexahydropyrrolo[1,2-c]pyrimidines

  摘要：

  Stereoselection in tethered Biginelli condensations can be tuned to give either the cia or trans stereoisomer of 1-oxohexahydropyrrolo[1,2-c]pyrimidine and 1-iminohexahydropyrrolo[1,2-c]pyrimidine products (see eq 1). With substrates having urea and N-sulfonylguanidine functionality (Schemes 2 and 4), cis stereoselection (4-7:1) is observed when the condensation is accomplished under Knoevenagel conditions, while trans stereoselection (4-20:1) is observed when the condensation is carried out in the presence of polyphosphate ester (PPE). Under both conditions, steroselectivity is highest in the N-sulfonylguanidine series. With substrates bearing a basic guanidine unit, the trans product is formed exclusively under Knoevenagel conditions (Scheme 3).

  DOI：

  10.1021/jo981972g