Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate
In the title compound, C17H22N2O5 the pyrrolidine ring is almost planar and subtends a dihedral angle of 85.77 (7) with the pendant phenyl ring. An intramolecular N—H O hydrogen bond generates an S(6) loop. In the crystal, the compound forms inversion dimers through O—H O hydrogen bonds from the dis...
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International Union of Crystallography
2024
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2-s2.0-85214395902 Abdul Rashid F.N.A.; Mohammat M.F.; Abdul Manan M.A.F.; Bakhtiar Afendy A.A.A.; Cordes D.B.; McKay A.P. Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate 2024 IUCrData 9 Pt 12 10.1107/S2414314624012227 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85214395902&doi=10.1107%2fS2414314624012227&partnerID=40&md5=7120a377d9ab6c288bba168fc3771f6a In the title compound, C17H22N2O5 the pyrrolidine ring is almost planar and subtends a dihedral angle of 85.77 (7) with the pendant phenyl ring. An intramolecular N—H O hydrogen bond generates an S(6) loop. In the crystal, the compound forms inversion dimers through O—H O hydrogen bonds from the disordered hydroxyl group to either the hydroxyl or ester carbonyl O atom of the adjacent molecule. © 2024 International Union of Crystallography. All rights reserved. International Union of Crystallography 24143146 English Data paper |
author |
Abdul Rashid F.N.A.; Mohammat M.F.; Abdul Manan M.A.F.; Bakhtiar Afendy A.A.A.; Cordes D.B.; McKay A.P. |
spellingShingle |
Abdul Rashid F.N.A.; Mohammat M.F.; Abdul Manan M.A.F.; Bakhtiar Afendy A.A.A.; Cordes D.B.; McKay A.P. Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate |
author_facet |
Abdul Rashid F.N.A.; Mohammat M.F.; Abdul Manan M.A.F.; Bakhtiar Afendy A.A.A.; Cordes D.B.; McKay A.P. |
author_sort |
Abdul Rashid F.N.A.; Mohammat M.F.; Abdul Manan M.A.F.; Bakhtiar Afendy A.A.A.; Cordes D.B.; McKay A.P. |
title |
Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate |
title_short |
Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate |
title_full |
Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate |
title_fullStr |
Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate |
title_full_unstemmed |
Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate |
title_sort |
Ethyl 4-[(2-hydroxyethyl)amino]-2-(4-methoxy-phenyl)-1-methyl-5-oxo-2,5-dihydro-1H-pyrrole-3-carboxylate |
publishDate |
2024 |
container_title |
IUCrData |
container_volume |
9 |
container_issue |
Pt 12 |
doi_str_mv |
10.1107/S2414314624012227 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85214395902&doi=10.1107%2fS2414314624012227&partnerID=40&md5=7120a377d9ab6c288bba168fc3771f6a |
description |
In the title compound, C17H22N2O5 the pyrrolidine ring is almost planar and subtends a dihedral angle of 85.77 (7) with the pendant phenyl ring. An intramolecular N—H O hydrogen bond generates an S(6) loop. In the crystal, the compound forms inversion dimers through O—H O hydrogen bonds from the disordered hydroxyl group to either the hydroxyl or ester carbonyl O atom of the adjacent molecule. © 2024 International Union of Crystallography. All rights reserved. |
publisher |
International Union of Crystallography |
issn |
24143146 |
language |
English |
format |
Data paper |
accesstype |
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record_format |
scopus |
collection |
Scopus |
_version_ |
1823296152457445376 |