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. Author manuscript; available in PMC: 2012 Oct 24.
Published in final edited form as: J Med Chem. 1989 Aug;32(8):1873–1879. doi: 10.1021/jm00128a031

Table III.

Synthesis and Characterization of Xanthine Derivatives

compd % yield mp, °C formula anal.
13 91 278 C12H16N4OS C, H, N
14 89 217 C16H24N4OS C, H, N
15a 80 347 C11HI0N4O3 C, H, N
15b 88 252 C15H18N4O3 C, H, N
15c 85 >350 C11H10N4O2S C, H, N
15d 88 269 C15H18N4O2S C, H, N
17 82 >300 C11H10N4O2S C, H, N
18 92 >300 C11H10N4O2S C, H, N
19 85 259 C15H18N4O2S C, H, N
20 87 267 C15H18N4O2S C, H, N
21 71 >340 C11H10N4O2S2 C, H, N
22 92 298 C15H18N4OS2 C, H, N
26a 91 >350 C13H12N4OS C, H, N
26b 80 253 C17H20N4OS C, H, N
33 95 206–208 C22H30N6O3S·¼H2O C, H, N
35 93 238–240 C23H32N6O3S·¾H2O C, H, N
37 52 172–174 C24H34N6O3S·½H2O C, H, N
39 92 210–212 C40H54N8O8S C, H, N
41 84 182–187 C37H47F3N8O8S·½CF3COOH·½H2O C, H, N
43 97 238–242 dec C27H40N8O4S·3HBr·3/2H2O C, H, N
45 68 160–168 C33H43N7O8S C, H, Nb
48 85 240 dec C27H31N6O5SI·2.5H2O C, H, N
52 85 236 C12H16N4S2 C, H, N
53 84 135 C16H24N4S2 C, H, N
54 79 241 C12H16N4OS C, H, N
55 81 153 C10H24N4OS C, H, N
56 84 256 C13H12N4OS C, H, N
57 72 223 C15H16N4OS H, C, Na
60b 84 230 C11H9NO3SHg C, H, N
61a 43  71–73 C6H5O2SI·0.5H2O C, H
a

C: calcd, 59.32; found, 58.52. N: calcd, 18.65; found, 18.12.

b

N: calcd, 14.05; found, 15.42.