反应 #531803

ord-a75aad1d06fd48879ecbff38eb160ad4

反应方程式

Cc1ccccc1C(=O)NC(CC(NC(=O)O)(c1occc(=O)c1OCc1ccccc1)c1occc(=O)c1OCc1ccccc1)c1occc(=O)c1OCc1ccccc1
4c
Cc1ccccc1C(=O)NC(CC(NC(=O)O)(c1occc(=O)c1OCc1ccccc1)c1occc(=O)c1OCc1ccccc1)c1occc(=O)c1OCc1ccccc1
N-(Tris(3-benzyloxy-4-oxo-4H-pyran-2-yl)carboxyaminopropyl)methyl benzamide
Cc1ccccc1C(=O)NC(CC(NC(=O)O)(c1occc(=O)c1O)c1occc(=O)c1O)c1occc(=O)c1O
title compound 6
收率 114.7%
Cc1ccccc1C(=O)NC(CC(NC(=O)O)(c1occc(=O)c1O)c1occc(=O)c1O)c1occc(=O)c1O
N-(Tris(-3-hydroxy-4-oxo-4H-pyran-2-yl)carboxyaminopropyl)methyl benzamide
收率 114.7%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The reaction mixture was concentrated in vacuo
  2. 2
    其他the residue azeotroped several times with methanol (10 ml)

实验过程

A solution of 4c (0.20 g, 0.20 mmol) in glacial acetic acid (2 ml) and concentrated hydrochloric acid (2 ml) was stirred at room temperature for 18 h. The reaction mixture was concentrated in vacuo, the residue azeotroped several times with methanol (10 ml) to afford the title compound 6 (130 mg, 90%) as a red-orange solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08475768B2uspto-grants-2013_07