1′-Methyl-5′-phenyl-2′',3′',5′',6′′-tetrahydroindoline-3-spiro-3′-pyrrolidine-4′-spiro-2′'-imidazo[2,1-b]thiazole-2,3′'-dione

Autor:	Gang Li, Ya-Qing Feng, Xiao-Fang Li, Da-Xin Shi
Rok vydání:	2003
Předmět:	Sarcosine biology Chemistry Stereochemistry Hydrogen bond Dimer Isatin General Chemistry Condensed Matter Physics Ring (chemistry) biology.organism_classification Pyrrolidine chemistry.chemical_compound Indoline Tetra General Materials Science
Zdroj:	Acta Crystallographica Section E Structure Reports Online. 59:o1288-o1289
ISSN:	1600-5368
Popis:	The title compound, C22H20N4O2S, was synthesized by the intermolecular [3 + 2]-cyclo­addition of azomethine yl­ide, derived from isatin and sarcosine by a de­carboxyl­ative route, and 2-benzyl­idene-5,6-di­hydro-imidazo­[2,1-b]­thia­zol-3-one. In the mol­ecule, the two spiro junctions link a planar 2-oxoindoline ring, a pyrrolidine ring in an envelope conformation, and a 5,6-di­hydro­imidazo­[2,1-b]­thia­zol-3(2H)-one ring. Two mol­ecules are connected into a dimer by two N—H⋯N hydrogen bonds.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::79f8a6f2f20a54be315a16898c0f6f0e https://doi.org/10.1107/s160053680301746x Zobrazit plný text záznamu Plný text