“…According to 1 H NMR stereoisomer ratio is 1.66:1. [ 36 ] - Major isomer 1 H NMR (400.13 MHz, DMSO- d 6 , ppm): 3.89 (s, 6H, CH 3 ), 3.95 (s, 3H, CH 3 ), 6.86–6.95 (m, 2H, H ind ), 7.24 (t, J = 7.6 Hz, 1H, H ind ), 7.27 (s, 2H, H 2′ ,H 6′ ), 7.79–7.83 (m, 2H, H ind ,CH=), 8.13 (br.s, 1H, NH).
- Selected peaks of minor isomer 1 H NMR (400.13 MHz, DMSO- d 6 , ppm): 3.98 (s, 9H, CH 3 ), 6.88 (d, J = 7.7 Hz, 1H, H 7 ) 7.06 (t, J = 7.4 Hz, 1H, H ind ), 7.49 (s, 1H, CH=), 7.54 (d, J = 7.5 Hz, 1H, H 4 ), 8.02 (br.s, 1H, NH)
- ( E , Z )-3-(3,5-Dimethoxy-4-hydroxybenzylidene)-5-benzoylamino-2-oxindole 26
- From 0.100 g (0.4 mmol) of 5-benzoylamino-oxindole, 0.089 g (0.4 mmol) of 3,5-dimethoxy-4-hydroxybenzaldehyde and 30 µL (0.35 mmol) of piperidine with ethanol as solvent the black powder (0.133 g, 79%) was obtained as a mixture of two isomers.
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