2-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid Phenylamide

2-Methyl-4-oxo-4,5-dihydro-1<i>H</i>-pyrrole-3-carboxylic acid phenylamide was obtained as a single product in an experiment on the cyclization modes of a glycine-derived enamino amide. High yield and operational simplicity are the main features of the presented synthetic procedure. Addi...

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Main Authors: Plamen Angelov, Pavel Yanev
Format: Article
Language:English
Published: MDPI AG 2024-02-01
Series:Molbank
Subjects:
Online Access:https://www.mdpi.com/1422-8599/2024/1/M1778
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author Plamen Angelov
Pavel Yanev
author_facet Plamen Angelov
Pavel Yanev
author_sort Plamen Angelov
collection DOAJ
description 2-Methyl-4-oxo-4,5-dihydro-1<i>H</i>-pyrrole-3-carboxylic acid phenylamide was obtained as a single product in an experiment on the cyclization modes of a glycine-derived enamino amide. High yield and operational simplicity are the main features of the presented synthetic procedure. Additionally, this result extends our previous observations on the cyclization reactions of similarly functionalized enamines, by revealing the preferred cyclization pathway under Boc-deprotection conditions.
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spelling doaj.art-63eb3b4a3f7f41cfb1d246ec716910b72024-03-27T13:56:38ZengMDPI AGMolbank1422-85992024-02-0120241M177810.3390/M17782-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid PhenylamidePlamen Angelov0Pavel Yanev1Department of Organic Chemistry, University of Plovdiv Paisii Hilendarski, 24 Tsar Asen Str., 4000 Plovdiv, BulgariaDepartment of Organic Chemistry, University of Plovdiv Paisii Hilendarski, 24 Tsar Asen Str., 4000 Plovdiv, Bulgaria2-Methyl-4-oxo-4,5-dihydro-1<i>H</i>-pyrrole-3-carboxylic acid phenylamide was obtained as a single product in an experiment on the cyclization modes of a glycine-derived enamino amide. High yield and operational simplicity are the main features of the presented synthetic procedure. Additionally, this result extends our previous observations on the cyclization reactions of similarly functionalized enamines, by revealing the preferred cyclization pathway under Boc-deprotection conditions.https://www.mdpi.com/1422-8599/2024/1/M1778pyrrole-3-carboxylic acidpyrrolin-4-oneβ-enaminoneamide
spellingShingle Plamen Angelov
Pavel Yanev
2-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid Phenylamide
Molbank
pyrrole-3-carboxylic acid
pyrrolin-4-one
β-enaminone
amide
title 2-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid Phenylamide
title_full 2-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid Phenylamide
title_fullStr 2-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid Phenylamide
title_full_unstemmed 2-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid Phenylamide
title_short 2-Methyl-4-Oxo-4,5-Dihydro-1<i>H</i>-Pyrrole-3-Carboxylic Acid Phenylamide
title_sort 2 methyl 4 oxo 4 5 dihydro 1 i h i pyrrole 3 carboxylic acid phenylamide
topic pyrrole-3-carboxylic acid
pyrrolin-4-one
β-enaminone
amide
url https://www.mdpi.com/1422-8599/2024/1/M1778
work_keys_str_mv AT plamenangelov 2methyl4oxo45dihydro1ihipyrrole3carboxylicacidphenylamide
AT pavelyanev 2methyl4oxo45dihydro1ihipyrrole3carboxylicacidphenylamide