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  4. Three-component synthesis of polysubstituted 6-azaindolines and its tricyclic derivatives
 
research article

Three-component synthesis of polysubstituted 6-azaindolines and its tricyclic derivatives

Fayol, Aude
•
Zhu, Jieping  
2005
Organic Letters

By simply heating a toluene soln. of isocyanoacetamide, amine, and aldehyde, a clean three-component reaction occurred to provide the 6-azaindolines and pyrrolidinone-fused 6-azaindolines. E.g., heating a mixt. of morpholine, heptanal, and isocyanoacetamide I gave 61% 6-azaindoline II. In this multicomponent reaction, the isocyanoacetamide reacted four times in a highly ordered manner creating three heterocyclic rings with the concurrent formation of five chem. bonds and a minimal loss of mol. wt. Heating is the only external energy required to promote this powerful complexity-generating MCR. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1021/ol0477881
Author(s)
Fayol, Aude
•
Zhu, Jieping  
Date Issued

2005

Published in
Organic Letters
Volume

7

Issue

2

Start page

239

End page

242

Subjects

Cyclization (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides

•

amines

•

and aldehydes); Aldehydes; Amines Role: RCT (Reactant)

•

RACT (Reactant or reagent) (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides

•

amines

•

and aldehydes); Isocyanides Role: RCT (Reactant)

•

SPN (Synthetic preparation)

•

PREP (Preparation)

•

RACT (Reactant or reagent) (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides

•

amines

•

and aldehydes)

•

azaindoline pyrrolidinone fused prepn; three component reaction isocyanoacetamide amine aldehyde

Note

CAN 142:197927

28-2

Heterocyclic Compounds (More Than One Hetero Atom)

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

Journal

written in English.

62-53-3 (Aniline); 100-46-9 (Benzylamine); 100-52-7 (Benzaldehyde); 109-73-9 (Butylamine); 110-89-4 (Piperidine); 110-91-8 (Morpholine); 111-71-7 (Heptanal); 120-20-7; 123-11-5 (4-Methoxybenzaldehyde); 555-16-8 (4-Nitrobenzaldehyde); 2043-61-0 (Cyclohexanecarbaldehyde); 3132-99-8 (3-Bromobenzaldehyde); 4289-95-6 (DL-Phenylalanine, n-formyl-); 17150-62-8; 67421-74-3; 123613-53-6; 142301-77-7 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides, amines, and aldehydes); 836678-76-3P; 836678-77-4P; 836678-78-5P; 836678-79-6P; 836678-80-9P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides, amines, and aldehydes); 836678-81-0P; 836678-82-1P; 836678-83-2P; 836678-84-3P; 836678-85-4P; 836678-86-5P; 836678-87-6P; 836678-88-7P; 836678-89-8P; 836678-90-1P; 836678-91-2P; 836678-92-3P; 836678-93-4P; 836678-94-5P; 836678-95-6P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of 6-azaindolines and pyrrolidinone-fused 6-azaindolines by three-component reaction of isocyanoacetamides, amines, and aldehydes)

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/20.500.14299/58466
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