反应详情

A solution of 4-(1,2,4-triazol-4yl)phenylhydrazine (25 g, 143 mmol) in dioxan (250 ml) was treated with dihydropyran (24 g, 286 mmol) followed by 1M hydrochloric acid (150 ml) and heated at reflux for 18 h. The reaction mixture was evaporated, treated with toluene the re-evaporated. Inorganic solids were removed by treating the residue with a mixture of methanol and acetonitrile. The mother liquors were purified by column chromatography on silica using dichloromethane/methanol (9:1→4:1) as the eluant. The compound was recrystallised from acetonitrile to afford the title compound as a colourless solid (10.24 g, 30%); mp 205-207° C. (Found: C, 64.37; H, 5.76; N, 22.83. C13H14N4O requires: C, 64.45; H, 5.82; N, 23.13%.) δH (360 MHz, DMSO-d6) 1.81 (2H, q, J=7 Hz, CH2), 2.75 (2H, t, J=8 Hz, CH2), 3.46 (2H, dt, J1 =6, J2 =5 Hz, CH2), 4.43 (1H, t, J=5 Hz, OH), 7.26 (1H, d, J=2 Hz, Ar-H), 7.29 (1H, dd, J1 =9, J2 =2 Hz, Ar-H), 7.47 (1H, d, J=9 Hz, Ar-H), 7.77 (1H, d, J=2 Hz, Ar-H), 9.01 (2H, s, triazole-H), 11.05 (1H, br s, indole NH); m/z (CI) 243 (M+ +1)

1. temperatureheated
2. temperatureat reflux for 18 h
3. customThe reaction mixture was evaporated
4. additiontreated with toluene the re-evaporated
5. customInorganic solids were removed
6. additionby treating the residue
7. additionwith a mixture of methanol and acetonitrile
8. customThe mother liquors were purified by column chromatography on silica
9. customThe compound was recrystallised from acetonitrile