تفاعل #531803

ord-a75aad1d06fd48879ecbff38eb160ad4

معادلة التفاعل

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
المردود 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
المردود 114.7%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08475768B2uspto-grants-2013_07