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3‐(4‐Chloro­phen­yl)‐5‐methyl‐2‐propyl­amino‐8,9,10,11‐tetra­hydro‐2‐benzothieno­[2′,3′;2,3]­pyrido[4,5‐d]pyrimidin‐4(3H)‐one

TLDR
The asymmetric unit of the title compound, C23H23ClN4OS, contains two crystallographically independent molcules in which the orientations of the propylamine group and chloro-phenyl rings with respect to the fused ring system are different as mentioned in this paper.
Abstract
The asymmetric unit of the title compound, C23H23ClN4OS, contains two crystallographically independent mol­ecules in which the orientations of the propyl­amine group and chloro­phenyl rings with respect to the fused ring system are different. The terminal cyclo­hexene ring adopts a half-chair conformation. The crystal packing is stabilized by N—H⋯O, N—H⋯N and C—H⋯O hydrogen bonds and π–π inter­actions.

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Journal ArticleDOI

Tin (IV) Chloride-promoted Synthesis of 4-Aminopyridines and 4-Aminoquinolines

TL;DR: Ortho-aminobenzonitriles as discussed by the authors react with β-ketoesters and alkyl malonates, in the presence of stoichiometric amounts of tin(IV) chloride, to give 4-aminoquinolines 2 and 4amino-2-quinolones 3 respectively.
Journal ArticleDOI

A new, general approach for the synthesis of heteroannulated 3,1-oxazin-4-ones

TL;DR: In this article, the β-(N-Triphenylphosphoranyliden)-enamino esters afford the synthetically useful heteroannulated 3,1-oxazin-4-ones with aroyl chlorides in different solvents.
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