Microwave‐assisted Groebke‐Blackburn‐Bienaymé multicomponent reaction to synthesize imidazo fused heterocycles via in‐situ generated isocyanides from N‐formylamines: An undergraduate organic laboratory experiment. (25th October 2021)
- Record Type:
- Journal Article
- Title:
- Microwave‐assisted Groebke‐Blackburn‐Bienaymé multicomponent reaction to synthesize imidazo fused heterocycles via in‐situ generated isocyanides from N‐formylamines: An undergraduate organic laboratory experiment. (25th October 2021)
- Main Title:
- Microwave‐assisted Groebke‐Blackburn‐Bienaymé multicomponent reaction to synthesize imidazo fused heterocycles via in‐situ generated isocyanides from N‐formylamines: An undergraduate organic laboratory experiment
- Authors:
- Kaur, Manpreet
Singh, Rahul
Patil, Madhuri T.
Kumar, Kushvinder
Sahoo, Subash Chandra
Singh, Kamal Nain
Chaudhari, Vinod D.
Salunke, Deepak B. - Abstract:
- Abstract: A one‐pot methodology is developed for the direct conversion of N ‐formylamine, 2‐amino pyridine, and aldehyde into 2, 3‐substituted imidazo[1, 2‐ a ]pyridine heterocycles using I2 ‐PPh3 ‐Et3 N reagent system under microwave irradiation. During the reaction, I2 ‐PPh3 ‐Et3 N converts N ‐formylamine into isocyanide, which in the presence of in‐situ generated hydrogen iodide (HI) undergoes Groebke‐Balckburn‐Bienaymé (GBB) multicomponent reaction with aldehyde and 2‐aminopyridine. The in‐situ generated HI eliminates the need for an external catalyst for the GBB reaction. The developed process incorporates the use of readily accessible and cheap reagents and also avoid a separate step for the synthesis of isocyanides having disagreeable odor. Fourteen different GBB based heterocycles have been synthesized to demonstrate the feasibility of the optimized protocol. The preparation of N ‐formylamines utilized in the synthesis is also elaborated and the overall process was optimized to be suitable for a typical undergraduate organic laboratory experiment. One of the final products was characterized using FT‐IR, 1 H NMR, 13 C NMR, DEPT, COSY, HSQC, HRMS, and single‐crystal X‐ray diffraction. Overall, the experiment will be useful in the organic chemistry curriculum to teach about multicomponent reactions, the importance of isocyanides in organic synthesis, formylation of amines, application of microwave irradiation in organic synthesis, and structural elucidation of smallAbstract: A one‐pot methodology is developed for the direct conversion of N ‐formylamine, 2‐amino pyridine, and aldehyde into 2, 3‐substituted imidazo[1, 2‐ a ]pyridine heterocycles using I2 ‐PPh3 ‐Et3 N reagent system under microwave irradiation. During the reaction, I2 ‐PPh3 ‐Et3 N converts N ‐formylamine into isocyanide, which in the presence of in‐situ generated hydrogen iodide (HI) undergoes Groebke‐Balckburn‐Bienaymé (GBB) multicomponent reaction with aldehyde and 2‐aminopyridine. The in‐situ generated HI eliminates the need for an external catalyst for the GBB reaction. The developed process incorporates the use of readily accessible and cheap reagents and also avoid a separate step for the synthesis of isocyanides having disagreeable odor. Fourteen different GBB based heterocycles have been synthesized to demonstrate the feasibility of the optimized protocol. The preparation of N ‐formylamines utilized in the synthesis is also elaborated and the overall process was optimized to be suitable for a typical undergraduate organic laboratory experiment. One of the final products was characterized using FT‐IR, 1 H NMR, 13 C NMR, DEPT, COSY, HSQC, HRMS, and single‐crystal X‐ray diffraction. Overall, the experiment will be useful in the organic chemistry curriculum to teach about multicomponent reactions, the importance of isocyanides in organic synthesis, formylation of amines, application of microwave irradiation in organic synthesis, and structural elucidation of small organic molecules. Abstract : … (more)
- Is Part Of:
- Journal of heterocyclic chemistry. Volume 59:Number 2(2022)
- Journal:
- Journal of heterocyclic chemistry
- Issue:
- Volume 59:Number 2(2022)
- Issue Display:
- Volume 59, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 59
- Issue:
- 2
- Issue Sort Value:
- 2022-0059-0002-0000
- Page Start:
- 319
- Page End:
- 328
- Publication Date:
- 2021-10-25
- Subjects:
- Heterocyclic compounds -- Periodicals
547.59 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/jhet.4386 ↗
- Languages:
- English
- ISSNs:
- 0022-152X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4998.200000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20780.xml