Skip to main content
. 2016 Apr 13;84(3):484–496. doi: 10.3390/scipharm84030484

Table 1.

RCO-, melting points (m.p.), and yields of N-acylbenzotriazoles 3a-k′ and N-acylcephalexines 4a-k′.

RCO-a–k′ 3a–k′ Yield % 3a–k′m.p. (°C) m.p. (°C) [Lit.] Time/h 4a–k′ 4a–k′ Yield % 4a–k′ m.p. (°C)
graphic file with name scipharm-84-00484-i001.jpg 94 107–109 (106–108) [24] 10 87 210–212
graphic file with name scipharm-84-00484-i002.jpg 95 150–153 (151–152) [24] 12 86 216–218
graphic file with name scipharm-84-00484-i003.jpg 95 99–101 (100–101) [25] 12 84 168–170
graphic file with name scipharm-84-00484-i004.jpg 94 111–112 (112–113) [14] 9 84 132–134
graphic file with name scipharm-84-00484-i005.jpg 94 101–102 (101–102) [15] 8 82 200–202
graphic file with name scipharm-84-00484-i006.jpg 90 156–157 (155–156) [16] 10 87 226–228
graphic file with name scipharm-84-00484-i007.jpg 96 125–127 (126–128) [17] 6 91 197–199
graphic file with name scipharm-84-00484-i008.jpg 87 175–176 12 86 125–127
graphic file with name scipharm-84-00484-i009.jpg 89 148–150 12 82 137–139
graphic file with name scipharm-84-00484-i010.jpg 82 107–110 20 89 179–181
graphic file with name scipharm-84-00484-i011.jpg 90 142–144 14 93 234–236
graphic file with name scipharm-84-00484-i012.jpg 90 142–144 14 89 224–227