【结 构 式】 |
【分子编号】52988 【品名】(2R)-2-[(2-(acetylamino)-6-{[(diphenylamino)carbonyl]oxy}-9H-purin-9-yl)methyl]-4,4-diethoxybutyl acetate 【CA登记号】n/a |
【 分 子 式 】C31H36N6O7 【 分 子 量 】604.66308 【元素组成】C 61.58% H 6% N 13.9% O 18.52% |
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:(XLIII)Yet another method was based on the alkylation of 2-N-acetyl-6-O-diphenylcarbamoylguanine (XLII) with tosylate (XXII) to give (XLIII). This was hydrolyzed to the precursor (XXV) by treatment with KOH.
【1】 Synthesis of acyclic nucleoside derivs.. WO 0008025 . |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(XXII) | 52971 | (2S)-4,4-diethoxy-2-({[(4-methylphenyl)sulfonyl]oxy}methyl)butyl acetate | C18H28O7S | 详情 | 详情 | |
(XXV) | 52974 | 2-amino-9-[(2R)-4,4-diethoxy-2-(hydroxymethyl)butyl]-1,9-dihydro-6H-purin-6-one | C14H23N5O4 | 详情 | 详情 | |
(XLII) | 37775 | 2-(acetamido)-9H-purin-6-yl diphenylcarbamate | C20H16N6O3 | 详情 | 详情 | |
(XLIII) | 52988 | (2R)-2-[(2-(acetylamino)-6-{[(diphenylamino)carbonyl]oxy}-9H-purin-9-yl)methyl]-4,4-diethoxybutyl acetate | n/a | C31H36N6O7 | 详情 | 详情 |
Extended Information