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  4. A Rapid Access to Biaryl Ether Containing Macrocycles by Pairwise Use of Ugi 4CR and Intramolecular SNAr-Based Cycloetherification
 
research article

A Rapid Access to Biaryl Ether Containing Macrocycles by Pairwise Use of Ugi 4CR and Intramolecular SNAr-Based Cycloetherification

Cristau, Pierre
•
Vors, Jean-Pierre
•
Zhu, Jieping  
2001
Organic Letters

An Ugi reaction promoted by ammonium chloride in aprotic solvent is documented here for the first time. From readily accessible starting materials, macrocycles with an endo aryl-aryl ether bond are synthesized in only two steps, Ugi four-component reaction (Ugi 4CR) and an intramol. SNAr reaction. The nitro group serves as an activator for the macrocyclization and provides a handle for the introduction of functional group diversity. For example, dipeptide amide I was obtained in an Ugi 4CR from isonitrile II, PhCHO, PhCH2NH2 and 3-hydroxyphenylacetic acid in the presence of NH4+Cl- in toluene at 0 Deg for 20 h. Cycloetherification of I took place in the presence of K2CO3 in DMF for 3 h to give macrocycle III in 80% yield. [on SciFinder (R)]

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Type
research article
DOI
10.1021/ol0168420
Author(s)
Cristau, Pierre
Vors, Jean-Pierre
Zhu, Jieping  
Date Issued

2001

Published in
Organic Letters
Volume

3

Issue

25

Start page

4079

End page

4082

Subjects

Addition reaction (Ugi; prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification); Ethers Role: SPN (Synthetic preparation)

•

PREP (Preparation) (arom.

•

macrocyclic; prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification); Macrocyclic compounds Role: SPN (Synthetic preparation)

•

PREP (Preparation) (biaryl ethers; prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification); Macrocyclization (etherification; prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification); Etherification (macrocyclization; prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification)

•

macrocycle biaryl ether prepn Ugi 4CR SNAr cycloetherification; Ugi four component reaction ammonium chloride reagent aprotic solvent; macrocyclization SNAr based etherification

Note

CAN 136:118732

34-3

Amino Acids, Peptides, and Proteins

Institut de Chimie des Substances Naturelles,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

75-31-0 (Isopropylamine); 78-84-2 (Iso-butyraldehyde); 100-46-9 (Benzylamine); 100-52-7 (Benzaldehyde); 104-53-0 (Benzenepropanal); 104-94-9 (p-Methoxyaniline); 109-73-9 (n-Butylamine); 111-71-7 (n-Heptanal); 120-20-7; 459-57-4 (4-Fluorobenzaldehyde); 621-37-4; 621-54-5; 3173-56-6 (Benzyl isocyanate); 15017-52-4; 58885-60-2 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification); 20274-69-5P; 42564-51-2P; 389634-80-4P; 389634-81-5P; 389634-82-6P; 389634-83-7P; 389634-84-8P; 389634-85-9P; 389634-86-0P; 389634-87-1P; 389634-88-2P; 389634-89-3P; 389634-97-3P; 389634-98-4P; 389634-99-5P; 389635-00-1P; 389635-01-2P; 389635-02-3P; 389635-04-5P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification); 389635-03-4P; 389635-05-6P; 389635-06-7P; 389829-05-4P; 389829-08-7P; 389829-10-1P; 389829-13-4P; 389829-15-6P; 389829-18-9P; 389829-21-4P; 389829-24-7P; 390360-55-1P; 390360-57-3P; 390360-59-5P; 390360-61-9P; 390360-63-1P; 390360-65-3P; 390360-67-5P; 390360-69-7P; 390360-71-1P; 390360-73-3P; 390360-75-5P; 390360-77-7P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of biaryl ether-contg. macrocycles by Ugi four component reaction and intramol. SNAr-based cycloetherification)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58513
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