Cargando…

5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide

The title compound, C(23)H(19)N(3)O(2), was synthesized by the 1,3-dipolar cyclo­addition reaction of N-phenyl-α-diazo­acetamide and chalcone. In the mol­ecule, the pyrazoline ring assumes an envelope conformation. Weak inter­molecular C—H⋯O hydrogen bonding is present in the crystal structure....

Descripción completa

Detalles Bibliográficos
Autor principal: He, Long
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970102/
https://www.ncbi.nlm.nih.gov/pubmed/21577674
http://dx.doi.org/10.1107/S1600536809034035
_version_ 1782190347141513216
author He, Long
author_facet He, Long
author_sort He, Long
collection PubMed
description The title compound, C(23)H(19)N(3)O(2), was synthesized by the 1,3-dipolar cyclo­addition reaction of N-phenyl-α-diazo­acetamide and chalcone. In the mol­ecule, the pyrazoline ring assumes an envelope conformation. Weak inter­molecular C—H⋯O hydrogen bonding is present in the crystal structure.
format Text
id pubmed-2970102
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29701022010-12-30 5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide He, Long Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(23)H(19)N(3)O(2), was synthesized by the 1,3-dipolar cyclo­addition reaction of N-phenyl-α-diazo­acetamide and chalcone. In the mol­ecule, the pyrazoline ring assumes an envelope conformation. Weak inter­molecular C—H⋯O hydrogen bonding is present in the crystal structure. International Union of Crystallography 2009-08-29 /pmc/articles/PMC2970102/ /pubmed/21577674 http://dx.doi.org/10.1107/S1600536809034035 Text en © Long He 2009 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
He, Long
5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide
title 5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide
title_full 5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide
title_fullStr 5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide
title_full_unstemmed 5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide
title_short 5-Benzoyl-N,4-diphenyl-4,5-dihydro-1H-pyrazole-3-carboxamide
title_sort 5-benzoyl-n,4-diphenyl-4,5-dihydro-1h-pyrazole-3-carboxamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970102/
https://www.ncbi.nlm.nih.gov/pubmed/21577674
http://dx.doi.org/10.1107/S1600536809034035
work_keys_str_mv AT helong 5benzoyln4diphenyl45dihydro1hpyrazole3carboxamide