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【结 构 式】

【分子编号】59213

【品名】 

【CA登记号】

【 分 子 式 】C25H51Cl2O3PS

【 分 子 量 】533.623302

【元素组成】C 56.27% H 9.63% Cl 13.29% O 8.99% P 5.8% S 6.01%

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)

Treatment of 2-decyloxy-3-(dodecylmercapto)-1-propanol (I) with phosphorus oxychloride in the presence of Et3N gave the intermediate dichlorophosphate ester (II). This was subsequently condensed with 3'-deoxy-3'-azidothymidine (AZT) (III) to produce, after aqueous hydrolysis, the target phosphate diester. The title diester was alternatively obtained by the phospholipase D-catalyzed condensation of AZT (III) with the choline monophosphate ester (IV).

1 Zilch, H.; Leinert, H.; Mertens, A.; Herrmann, D. (Roche Diagnostics GmbH); New phospholipid derivs. of nucleosides, their preparation and their use as antiviral drugs. DE 4026265; EP 0545966; JP 1994500546; WO 9203462 .
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) 59212 2-(decyloxy)-3-(dodecylsulfanyl)-1-propanol C25H52O2S 详情 详情
(II) 59213   C25H51Cl2O3PS 详情 详情
(III) 25317 1-[(2R,4S,5S)-4-azido-5-(hydroxymethyl)tetrahydro-2-furanyl]-5-methyl-2,4(1H,3H)-pyrimidinedione 101703-35-9 C10H13N5O4 详情 详情
(IV) 59214 9-(decyloxy)-2,2-dimethyl-6-oxo-5,7-dioxa-11-thia-2-azonia-6lambda~5~-phosphatricosan-6-olate C30H64NO5PS 详情 详情
Extended Information