(11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione
The title chiral compound, C13H14N2O4, was prepared by an intracyclization reaction of methyl (S)-1-(4-hydroxy-5-methoxy-2-nitrobenzyl)-5-oxopyrrolidine-2-carboxylate in the presence of ethanol and iron. The five-membered substituted pyrrole ring adopts an approximate envelope conformation, while th...
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International Union of Crystallography
2008-01-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536807066056 |
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doaj-81d6384be5a94e1dbdb74b991140aea22020-11-25T01:50:34ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682008-01-01641o266o26610.1107/S1600536807066056(11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dioneDong-Mei ZhaoChao MaYu ShaJing-Hong LiuMao-Sheng ChengThe title chiral compound, C13H14N2O4, was prepared by an intracyclization reaction of methyl (S)-1-(4-hydroxy-5-methoxy-2-nitrobenzyl)-5-oxopyrrolidine-2-carboxylate in the presence of ethanol and iron. The five-membered substituted pyrrole ring adopts an approximate envelope conformation, while the seven-membered substituted diazepine ring displays a twist-boat conformation. Intermolecular O—H...O and N—H...O hydrogen bonding helps to stabilize the crystal structure.http://scripts.iucr.org/cgi-bin/paper?S1600536807066056 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dong-Mei Zhao Chao Ma Yu Sha Jing-Hong Liu Mao-Sheng Cheng |
spellingShingle |
Dong-Mei Zhao Chao Ma Yu Sha Jing-Hong Liu Mao-Sheng Cheng (11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione Acta Crystallographica Section E |
author_facet |
Dong-Mei Zhao Chao Ma Yu Sha Jing-Hong Liu Mao-Sheng Cheng |
author_sort |
Dong-Mei Zhao |
title |
(11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione |
title_short |
(11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione |
title_full |
(11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione |
title_fullStr |
(11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione |
title_full_unstemmed |
(11aS)-8-Hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1H-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione |
title_sort |
(11as)-8-hydroxy-7-methoxy-2,3,5,10,11,11a-hexahydro-1h-pyrrolo[2,1-c][1,4]benzodiazepine-3,11-dione |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2008-01-01 |
description |
The title chiral compound, C13H14N2O4, was prepared by an intracyclization reaction of methyl (S)-1-(4-hydroxy-5-methoxy-2-nitrobenzyl)-5-oxopyrrolidine-2-carboxylate in the presence of ethanol and iron. The five-membered substituted pyrrole ring adopts an approximate envelope conformation, while the seven-membered substituted diazepine ring displays a twist-boat conformation. Intermolecular O—H...O and N—H...O hydrogen bonding helps to stabilize the crystal structure. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536807066056 |
work_keys_str_mv |
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