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10,13‐Bis( p ‐tolylsulfonyl)‐1,4,7‐trithia‐10,13‐diazacyclopentadecane
Author(s) -
Blake Alexander J.,
Lippolis Vito,
Schröder Martin
Publication year - 2004
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536804009201
Subject(s) - tosyl , chemistry , decane , sulfonyl , amide , amine gas treating , molecule , ring (chemistry) , sulfide , medicinal chemistry , tetra , stereochemistry , organic chemistry , alkyl
The title compound, C 24 H 34 N 2 O 4 S 5 , is the ditosylated precursor to the mixed aza–thia macrocycle 1,4,7‐trithia‐10,13‐diazacyclopentadecane ([15]aneN 2 S 3 ) and is prepared by reacting bis(2‐mercaptoethyl) sulfide with O,O ′, N,N ′‐tetratosyl‐ N,N ′‐bis(2‐oxyethyl)ethylendiamine in dimethylformamide in the presence of Cs 2 CO 3 . Molecules lie across crystallographic twofold axes. The macrocyclic framework adopts a [] conformation and the two tolylsulfonyl groups are directed away from the ring cavity. There is extensive disorder of the methylene groups of the macrocyclic backbone.

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