反応 #706399

反応方程式

2,4-Diamino-6-chloro-5-nitropyrimidine

sodium

benzyl alcohol

→

2,4-Diamino-6-benzyloxy-5-nitropyrimidine

反応条件

後処理

1. 1
   その他the solvent was evaporated under reduced pressure
2. 2
   その他to provide a yellow solid
3. 3
   洗浄This solid was washed with water, and air
4. 4
   その他dried
5. 5
   その他Crystallization from benzene/ether
6. 6
   その他gave a pale yellow filamentous solid
7. 7
   その他yield
8. 8
   その他mp 194-195° C. (171° C.; Kosary et. al., Acta. Phazm. Hung., 49, 241-247 (1989))

実験手順

2,4-Diamino-6-chloro-5-nitropyrimidine (O'Brien et. al., J. Med. Chem., 9, 573-575 (1966)) (1.0 g, 5.28 mmol) was added to a solution of sodium (0.14 g, 6.08 mmol) in benzyl alcohol (9 mL). The solution was heated in a 160° C. oil bath for 3.5 h and the solvent was evaporated under reduced pressure to provide a yellow solid. This solid was washed with water, and air dried. Crystallization from benzene/ether gave a pale yellow filamentous solid: yield, 0.69 g (50%); mp 194-195° C. (171° C.; Kosary et. al., Acta. Phazm. Hung., 49, 241-247 (1989)); UV (pH 1) lmax 236 nm (sh) (e=1.452×104), 264 (0.522×104), 321 (1.294×104); (pH 6.9) 242 (sh) (0.965×104), 337 (1.493×104); (pH 13) 242 (sh) (0.952×104), 338 (1.479×104); 1H NMR d 5.43 (s, 2 H, ArCH2), 7.26 (br s, 2 H, NH2, exchange with D2O), 7.33-7.51 (m, 5 H, ArH), 7.93 (br s, 2 H, NH2, exchange with D2O); MS (EI) calcd. m/z for C11H11N5O3 261.0861, found 261.0866; Anal. (C11H11N5O3).

出典