【结 构 式】 |
【分子编号】38257 【品名】2,2-dimethylpropanethioic S-acid 【CA登记号】 |
【 分 子 式 】C5H10OS 【 分 子 量 】118.1998 【元素组成】C 50.81% H 8.53% O 13.54% S 27.13% |
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:(I)The esterification of 2,2-dimethyl-thiopropionic acid (I) with 2-iodoethanol (II) and DBU in toluene gives the corresponding thioester (III), which is condensed with diisopropylamidophosphoryl dichloride (IV) by means of TEA in THF to afford the phosphoramidite (V). Finally, this compound is condensed with AZT (VI) by means of 1H-tetrazole and MCPBA or 1H-tetrazole and tert-butyl peroxide, both cases in THF.
【1】 Lefebvre, I.; et al.; Mononucleoside phosphotriester derivatives with S-acyl-2-thioethyl bioreversible phosphate-protecting groups: Intracellular delivery of 3'-azido-2',3'-dideoxythymidine 5'-monophosphate. J Med Chem 1995, 38, 20, 3941. |
【2】 Lannuzel, M.; et al.; Synthesis of the tBuSATE pronucleotide of AZT by two different synthetic approaches. Nucleosides Nucleotides 1999, 18, 4-5, 1001. |
【3】 Lefebvre, I.; et al.; Synthesis, descomposition pathways and "in vitro" evaluation of bioreversible phosphotriesters of AZT. Nucleosides Nucleotides 1995, 14, 3-5, 763. |
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) | 38257 | 2,2-dimethylpropanethioic S-acid | C5H10OS | 详情 | 详情 | |
(II) | 38258 | 2-iodo-1-ethanol | 624-76-0 | C2H5IO | 详情 | 详情 |
(III) | 38259 | S-(2-hydroxyethyl) 2,2-dimethylpropanethioate | C7H14O2S | 详情 | 详情 | |
(IV) | 38260 | C6H14Cl2NOP | 详情 | 详情 | ||
(V) | 38261 | S-[4-(diisopropylamino)-10,10-dimethyl-4,9-dioxo-3,5-dioxa-8-thia-4lambda(5)-phosphaundec-1-yl] 2,2-dimethylpropanethioate | C20H40NO5PS2 | 详情 | 详情 | |
(VI) | 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 |
Extended Information