【结 构 式】 |
【分子编号】12075 【品名】3-(Benzyloxy)-1,2-dimethyl-4(1H)-pyridinone 【CA登记号】 |
【 分 子 式 】C14H15NO2 【 分 子 量 】229.27864 【元素组成】C 73.34% H 6.59% N 6.11% O 13.96% |
与该中间体有关的原料药合成路线共 1 条
合成路线1
该中间体在本合成路线中的序号:(II)A new synthesis of L1 has been reported: The reaction of 3-benzyloxy-2-methyl-4H-pyran-4-one (I) with methylamine and NaOH in refluxing ethanol gives 3-benzyloxy-1,2-dimethylpyridin-4(1H)-one (II), which is deprotected by hydrogenolysis with H2 over Pd/C in ethanol.
【1】 Dobbin, P.S.; Hider, R.C.; Porter, J.B.; Sarpong, P.; Hall, A.D.; Xiao, G.; Taylor, P.D.; Van der Helm, D.; Synthesis, physicochemical properties, and biological evaluation of N-substituted 2-alkyl-3-hydroxy-4(1H)-pyridinones: Orally active iron chelators with clinical potential. J Med Chem 1993, 36, 17, 2448. |
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