| 1217899-67-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• CAS: 1217899-67-6
• 化学式: C₃₂H₂₂N₂O₃S
• 分子量: 514.604
• InChiKey: FQDCILIZFTVCNT-UHFFFAOYSA-N

反应信息

• 作为反应物：
  描述：

  在 sodium tetrahydroborate 作用下， 以 乙醇 为溶剂， 以70%的产率得到
  参考文献：
  名称：

  Phenylfurylthieno[2,3-b]pyridyl-methanes. synthesis and reactions of the furan ring transformation

  摘要：

  Triarylmethane derivatives with various substituents, phenyl, 5-methyl-2-furyl, and 3-acylaminothieno[2,3-b] pyrid-2-yl have been obtained for the first time. The behavior of these compounds under protolytic conditions has been studied. It was shown that the character of the protection of the amino group of the thienopyridine fragment affects the type of transformation of the furan ring.

  DOI：

  10.1007/s10593-009-0401-9
• 作为产物：
  描述：

  、 苯甲酰氯 以 氯苯 为溶剂， 以60%的产率得到
  参考文献：
  名称：

  Phenylfurylthieno[2,3-b]pyridyl-methanes. synthesis and reactions of the furan ring transformation

  摘要：

  Triarylmethane derivatives with various substituents, phenyl, 5-methyl-2-furyl, and 3-acylaminothieno[2,3-b] pyrid-2-yl have been obtained for the first time. The behavior of these compounds under protolytic conditions has been studied. It was shown that the character of the protection of the amino group of the thienopyridine fragment affects the type of transformation of the furan ring.

  DOI：

  10.1007/s10593-009-0401-9