反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 90 °C
PROCEDURE
实验过程
2-{4-[(R)-3-(2,4-Dimethyl-phenoxy)-2-hydroxy-propylamino]-6-oxo-1,6-dihydro-pyrimidin-5-yl}-6-(1-methyl-piperidin-4-yl)-1H-1,3,6-triaza-s-indacene-5,7-dione (60.1 mg, 0.105 mmol) was mixed with zinc dust (300 mg) in AcOH (12 mL) resulting a mixture which was heated at 90° C. for 1 h, then cooled to the room temperature and filtered. The filtrate was evaporated, the residue was basified with NH3 in EtOH (2 M) and purified by chromatography with CH2Cl2/MeOH/28% aqueous NH4OH (60:10:1) to furnish a fluorescent product which was subjected to HPLC purification to afford the title compound in TFA salt form (42 mg, 60%). 1H NMR (DMSO-d6) δ 1.90-2.15 (4H), 2.13 (s, 3H, CH3), 2.20 (s, 3H, CH3), 2.81 (s, 3H, CH3), 3.20 (m, 2H), 3.40-3.60 (4H), 3.97 (m, 2H), 4.13 (m, 1H), 4.31 (m, 1H), 4.40 (s, 2H), 4.46 (s, 2H), 6.83 (d, J=6 Hz, 1H), 6.93 (d, J=6 Hz, 1H), 6.96 (s, 1H), 7.53 (br s, 1H), 7.75 (s, 1H), 9.75 (br s, 1H); ESI-MS m/z 560.5 (MH+).
WORKUP
后处理
- customresulting a mixture which
- temperaturecooled to the room temperature
- filtrationfiltered
- customThe filtrate was evaporated
- custompurified by chromatography with CH2Cl2/MeOH/28% aqueous NH4OH (60:10:1)
- customto furnish a fluorescent product which
- customwas subjected to HPLC purification