Reaktion #531803

ord-a75aad1d06fd48879ecbff38eb160ad4

Reaktionsgleichung

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
Ausbeute 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
Ausbeute 114.7%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture was concentrated in vacuo
  2. 2
    Sonstigethe residue azeotroped several times with methanol (10 ml)

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08475768B2uspto-grants-2013_07