<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>68(Pt 4)</volume><submitter>Fun HK</submitter><pubmed_abstract>In the title compound, C(20)H(21)N(3)O(4), the 1,4-dihydro-pyridine ring adopts a boat conformation. An intra-molecular C-H⋯O hydrogen bond generates an S(6) ring motif. The pyrazole ring makes dihedral angles of 87.81 (7) and 45.09 (7)° with the mean plane of the 1,4-dihydro-pyridine ring and the phenyl ring, respectively. In the crystal, mol-ecules are linked by N-H⋯N, N-H⋯O and C-H⋯O hydrogen bonds into a three-dimensional network.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o922-3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3343908</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Dimethyl 2,6-dimethyl-4-(3-phenyl-1H-pyrazol-4-yl)-1,4-dihydro-pyridine-3,5-dicarboxyl-ate.</pubmed_title><pmcid>PMC3343908</pmcid><pubmed_authors>Fun HK</pubmed_authors><pubmed_authors>Shivananda KN</pubmed_authors><pubmed_authors>Isloor AM</pubmed_authors><pubmed_authors>Arshad S</pubmed_authors><pubmed_authors>Malladi S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dimethyl 2,6-dimethyl-4-(3-phenyl-1H-pyrazol-4-yl)-1,4-dihydro-pyridine-3,5-dicarboxyl-ate.</name><description>In the title compound, C(20)H(21)N(3)O(4), the 1,4-dihydro-pyridine ring adopts a boat conformation. An intra-molecular C-H⋯O hydrogen bond generates an S(6) ring motif. The pyrazole ring makes dihedral angles of 87.81 (7) and 45.09 (7)° with the mean plane of the 1,4-dihydro-pyridine ring and the phenyl ring, respectively. In the crystal, mol-ecules are linked by N-H⋯N, N-H⋯O and C-H⋯O hydrogen bonds into a three-dimensional network.</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Apr</publication><modification>2025-04-04T09:11:50.133Z</modification><creation>2019-03-27T00:53:03Z</creation></dates><accession>S-EPMC3343908</accession><cross_references><pubmed>22589989</pubmed><doi>10.1107/S1600536812008306</doi></cross_references></HashMap>