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(S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate
The title chiral compound, C(14)H(16)N(2)O(2), was prepared by esterification of (S)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-1-carboxylic acid in the presence of HCl/EtOH. In the molecule, the quinazoline ring is non-planar and exhibits a distorted half-chair conformation, while the five-memb...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961280/ https://www.ncbi.nlm.nih.gov/pubmed/21202305 http://dx.doi.org/10.1107/S1600536808008908 |
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author | Ma, Chao Du, Gui-Jie Tian, Yu Sha, Yu Cheng, Mao-Sheng |
author_facet | Ma, Chao Du, Gui-Jie Tian, Yu Sha, Yu Cheng, Mao-Sheng |
author_sort | Ma, Chao |
collection | PubMed |
description | The title chiral compound, C(14)H(16)N(2)O(2), was prepared by esterification of (S)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-1-carboxylic acid in the presence of HCl/EtOH. In the molecule, the quinazoline ring is non-planar and exhibits a distorted half-chair conformation, while the five-membered ring shows a typical envelope conformation. Intermolecular C—H⋯N hydrogen bonding helps to stabilize the crystal structure. |
format | Text |
id | pubmed-2961280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29612802010-12-30 (S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate Ma, Chao Du, Gui-Jie Tian, Yu Sha, Yu Cheng, Mao-Sheng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title chiral compound, C(14)H(16)N(2)O(2), was prepared by esterification of (S)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolin-1-carboxylic acid in the presence of HCl/EtOH. In the molecule, the quinazoline ring is non-planar and exhibits a distorted half-chair conformation, while the five-membered ring shows a typical envelope conformation. Intermolecular C—H⋯N hydrogen bonding helps to stabilize the crystal structure. International Union of Crystallography 2008-04-10 /pmc/articles/PMC2961280/ /pubmed/21202305 http://dx.doi.org/10.1107/S1600536808008908 Text en © Ma et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Ma, Chao Du, Gui-Jie Tian, Yu Sha, Yu Cheng, Mao-Sheng (S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate |
title | (S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate |
title_full | (S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate |
title_fullStr | (S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate |
title_full_unstemmed | (S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate |
title_short | (S)-Ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate |
title_sort | (s)-ethyl 1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961280/ https://www.ncbi.nlm.nih.gov/pubmed/21202305 http://dx.doi.org/10.1107/S1600536808008908 |
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