<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>51</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>64(Pt 1)</volume><submitter>Song DD</submitter><pubmed_abstract>In the title compound, C(22)H(21)ClN(4)O(2)S, the bicyclic triazolopyrimidine ring system is nearly planar, and oriented at dihedral angles of 89.45?(3)° with respect to the chlorobenzene ring and 87.03?(3)° with respect to the terminal phenyl ring. In the crystal structure, mol-ecules are linked by ?-? stacking inter-actions between the triazolopyrimidine rings [centroid-centroid distances of 3.88?(1) and 3.63?(1)?Å].</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2915002</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ethyl 2-benzyl-sulfanyl-7-(2-chloro-phen-yl)-5-methyl-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxyl-ate.</pubmed_title><pmcid>PMC2915002</pmcid><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Song DD</pubmed_authors><view_count>51</view_count></additional><is_claimable>false</is_claimable><name>Ethyl 2-benzyl-sulfanyl-7-(2-chloro-phen-yl)-5-methyl-4,7-dihydro-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxyl-ate.</name><description>In the title compound, C(22)H(21)ClN(4)O(2)S, the bicyclic triazolopyrimidine ring system is nearly planar, and oriented at dihedral angles of 89.45?(3)° with respect to the chlorobenzene ring and 87.03?(3)° with respect to the terminal phenyl ring. In the crystal structure, mol-ecules are linked by ?-? stacking inter-actions between the triazolopyrimidine rings [centroid-centroid distances of 3.88?(1) and 3.63?(1)?Å].</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Dec</publication><modification>2021-02-20T23:33:21Z</modification><creation>2019-03-27T00:32:56Z</creation></dates><accession>S-EPMC2915002</accession><cross_references><pubmed>21200919</pubmed><doi>10.1107/S1600536807062174</doi></cross_references></HashMap>