Skip to main content
. 2022 Nov 24;12(52):33772–33779. doi: 10.1039/d2ra06469c

Compounds 4a–e and 6a–ca.

Entry Diamine Product Time (min) Yield (%) Mp (°C)
1 graphic file with name d2ra06469c-u2.jpg graphic file with name d2ra06469c-u3.jpg 10 98 227–229
2 graphic file with name d2ra06469c-u4.jpg graphic file with name d2ra06469c-u5.jpg 25 76 240–242
3 graphic file with name d2ra06469c-u6.jpg graphic file with name d2ra06469c-u7.jpg 30 85 280–282
4 graphic file with name d2ra06469c-u8.jpg graphic file with name d2ra06469c-u9.jpg 15 80 231–233
5 graphic file with name d2ra06469c-u10.jpg graphic file with name d2ra06469c-u11.jpg 20 73 278–280
6 graphic file with name d2ra06469c-u12.jpg graphic file with name d2ra06469c-u13.jpg 120 84 314–317
7 graphic file with name d2ra06469c-u14.jpg graphic file with name d2ra06469c-u15.jpg 90 82 241–243
8 graphic file with name d2ra06469c-u16.jpg graphic file with name d2ra06469c-u17.jpg 100 78 185–188
a

The reactions were performed using ninhydrin (1 mmol), malononitrile (1 mmol), diamine (1 mmol), H2O (10 ml).