“…The structures of the new compounds were characterized by a combination of elemental analysis and 1 H NMR, 13 C NMR, IR, and MS spectral data. The reaction of 27,28-dibromo-6,7,9,10,12,13,16,17,23,24,31,32-dodecahydro-5H,15H-tribenzo[b,h,w] [1,4,7,13,16,19,25,10,22]dioxapentathiadiazacycloheptacosine 1 with 3 equivalents of chloroacetic anhydride in dichloromethane at 0-5 • C under argon atmosphere afforded 1,1'- (27,28-dibromo-6,7,9,10,12,13,15,16,23,24,31,32-dodecahydrotribenzo[b,h,w] [1,4,7,13,16,19,25,10,22]dioxapentathiadiazacycloheptacosine-5,17-diyl)bis(2-chloroethanone) 2 in 90% yield. A free -NH stretching vibration at 3346 cm −1 in the IR spectrum of precursor compound 1 24 disappeared after the introduction of chloroacetic anhydride as amide function.…”