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【结 构 式】

【分子编号】66794

【品名】2-(((tert-butyldiphenylsilyl)oxy)methyl)-5-methoxytetrahydrofuran-3-ol

【CA登记号】 

【 分 子 式 】C22H30O4Si

【 分 子 量 】386.5633

【元素组成】C 68.36% H 7.82% O 16.56% Si 7.27%

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:(VII)

 

1 Storer R. Moussa A. Wang JY. et al. 2005. Synthesis of β-L-2-deoxy-nucleosides from furanoses and pyranoses via a chloro-sugar and anhydro-l-furanosyl-nucleobase intennediatcs as potential antiviral and antineoplastic agents. W0 2005003374
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(X) 12204 5-Methyl-2,4(1H,3H)-pyrimidinedione; Thymine 65-71-4 C5H6N2O2 详情 详情
(I) 17901 Ethyl 3,3-diethoxypropanoate 10601-80-6 C9H18O4 详情 详情
(II) 66789 3,3-diethoxypropanal   C7H14O3 详情 详情
(III) 66790 (E)-5,5-diethoxypent-2-en-1-ol   C9H18O3 详情 详情
(IV) 66791 (3-(2,2-diethoxyethyl)oxiran-2-yl)methanol   C9H18O4 详情 详情
(V) 66792 tert-butyl((3-(2,2-diethoxyethyl)oxiran-2-yl)methoxy)diphenylsilane   C25H36O4Si 详情 详情
(VI) 66793 5-((tert-butyldiphenylsilyl)oxy)-3,4-dihydroxypentanal   C21H28O4Si 详情 详情
(VII) 66794 2-(((tert-butyldiphenylsilyl)oxy)methyl)-5-methoxytetrahydrofuran-3-ol   C22H30O4Si 详情 详情
(VIII) 62915 {(2S,3R)-5-methoxy-3-[(4-methylbenzoyl)oxy]tetrahydro-2-furanyl}methyl 4-methylbenzoate C22H24O6 详情 详情
(IX) 37194 (2R,3S)-5-Chloro-2-[[(4-methylbenzoyl)oxy]methyl]tetrahydro-3-furanyl 4-methylbenzoate 4330-21-6 C21H21ClO5 详情 详情
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