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【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