【结 构 式】 |
【分子编号】10354 【品名】2-Amino-9-([2-[(trimethylsilyl)oxy]ethoxy]methyl)-1,9-dihydro-6H-purin-6-one 【CA登记号】 |
【 分 子 式 】C11H19N5O3Si 【 分 子 量 】297.38926 【元素组成】C 44.43% H 6.44% N 23.55% O 16.14% Si 9.44% |
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:(IV)An efficient and selective process for the synthesis of acyclovir has been published: The reaction of guanine (I) with refluxing hexamethyldisilazane (HMDS) (II) by means of trifluoromethanesulfonic acid, elimination of the HMDS in excess and condensation of the resulting product with refluxing 1,3-dioxolane (III) gives 9-[2-(trimethylsilyloxy)ethoxymethyl]guanine (IV), which is finally hydrolyzed with refluxing acetic acid/water.
【1】 Han, Y.-K.; Harrington, P.J.; Schloemer, G.C. (F. Hoffmann-La Roche AG); Preparation of acyclovir. EP 0709385; JP 1996053451 . |
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