【结 构 式】 |
【分子编号】66314 【品名】(allyloxy)(tert-butyl)diphenylsilane 【CA登记号】 |
【 分 子 式 】C19H24OSi 【 分 子 量 】296.484 【元素组成】C 76.97% H 8.16% O 5.40% Si 9.47% |
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:(III)
【1】 Liotta DC, Schinazi RF, et al.1993. The preparation of 2'-deoxy-5-fluoro-3'-thiacytidine and related compounds as anti-HIV nucleosides. US 5210085 |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(I) | 12234 | 2-Propen-1-ol; Allyl alcohol | 107-18-6 | C3H6O | 详情 | 详情 |
(II) | 66313 | tert-Butylchlorodiphenylsilane;tert-Butyldiphenylchlorosilane;tert-Butyldiphenylsilyl chloride | 58479-61-1 | C16H19ClSi | 详情 | 详情 |
(III) | 66314 | (allyloxy)(tert-butyl)diphenylsilane | C19H24OSi | 详情 | 详情 | |
(IV) | 44475 | 2-[[tert-butyl(diphenyl)silyl]oxy]acetaldehyde | C18H22O2Si | 详情 | 详情 | |
(V) | 18524 | 2-sulfanylacetic acid | 68-11-1 | C2H4O2S | 详情 | 详情 |
(VI) | 66315 | 2-(((tert-butyldiphenylsilyl)oxy)methyl)-1,3-oxathiolan-5-one | C20H24O3SSi | 详情 | 详情 | |
(VII) | 55072 | (2R)-2-({[tert-butyl(diphenyl)silyl]oxy}methyl)-1,3-oxathiolan-4-yl acetate | C22H28O4SSi | 详情 | 详情 | |
(VIII) | 36959 | 5-fluoro-N-(trimethylsilyl)-2-[(trimethylsilyl)oxy]-4-pyrimidinamine; N-[5-fluoro-2-[(trimethylsilyl)oxy]-4-pyrimidinyl]-N-(trimethylsilyl)amine | C10H20FN3OSi2 | 详情 | 详情 | |
(IX) | 66316 | 4-amino-1-((2S,5R)-2-(((tert-butyldiphenylsilyl)oxy)methyl)-1,3-oxathiolan-5-yl)-5-fluoropyrimidin-2(1H)-one | C24H28FN3O3SSi | 详情 | 详情 |
Extended Information