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【结 构 式】

【分子编号】42818

【品名】 

【CA登记号】

【 分 子 式 】C9H12Cl2N3O5PS

【 分 子 量 】376.156662

【元素组成】C 28.74% H 3.22% Cl 18.85% N 11.17% O 21.27% P 8.23% S 8.52%

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:(II)

The condensation of 1-(beta-D-arabinofuranosyl)-2-thiocytosine (I) with phosphoryl chloride gave intermediate (II). Acid chloride (II) was then condensed with myristyl alcohol (III) to furnish the desired phosphate ester, which was finally converted to the title sodium salt by treatment with aqueous NaOH.

1 Kawaguchi, T.; et al.; Enzymatic reactivity and anti-tumor activity of 1-(beta-D-arabinofuranosyl)-2-thiocytosine derivatives. Chem Pharm Bull 2000, 48, 4, 454.
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) 42817 4-amino-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-2(1H)-pyrimidinethione 13239-97-9 C9H13N3O4S 详情 详情
(II) 42818   C9H12Cl2N3O5PS 详情 详情
(III) 42819 1-tetradecanol 112-72-1 C14H30O 详情 详情
Extended Information