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【结 构 式】

【分子编号】59476

【品名】tert-butyl(dimethyl)silyl [4-(2-propynyl)cyclohexyl]methyl ether; tert-butyl(dimethyl){[4-(2-propynyl)cyclohexyl]methoxy}silane

【CA登记号】

【 分 子 式 】C16H30OSi

【 分 子 量 】266.4991

【元素组成】C 72.11% H 11.35% O 6% Si 10.54%

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:(XIV)

1,4-Cyclohexanedimethanol (X) was converted to the mono-tosylate (XI), which was then condensed with lithium acetylide ethylenediamine complex to furnish (4-propargylcyclohexyl)methanol (XII). This procedure was further improved with the protection of diol (X) as the mono-silyl ether (XIII). Tosylation of (XIII) and subsequent reaction with lithium acetylide afforded (XIV), which was then desilylated to (XII) by means of tetrabutylammonium fluoride. Alcohol (XII) was oxidized by Jones reagent to the corresponding carboxylic acid (XV). This was converted into the methyl ester (XVI) by treatment with trimethylsilyl diazomethane. Finally, palladium-catalyzed coupling of the iodopurine (IX) with acetylene (XVI) gave rise to the title compound.

1 Sullivan, G.W.; Rieger, J.M.; Brown, M.L.; Macdonald, T.L.; Linden, J.; Design, synthesis, and evaluation of novel A2A adenosine receptor agonists. J Med Chem 2001, 44, 4, 531.
2 Linden, J.M.; MacDonald, T.; Glover, D.K.; Beller, G.A. (University of Virginia); Induction of pharmacological stress with adenosine receptor agonists. JP 2003502433; WO 0078774 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 22401 (2S,3S,4R,5R)-5-(6-amino-2-iodo-9H-purin-9-yl)-N-ethyl-3,4-dihydroxytetrahydro-2-furancarboxamide C12H15IN6O4 详情 详情
(X) 59472 [4-(hydroxymethyl)cyclohexyl]methanol C8H16O2 详情 详情
(XI) 59473 [4-(hydroxymethyl)cyclohexyl]methyl 4-methylbenzenesulfonate C15H22O4S 详情 详情
(XII) 59474 [4-(2-propynyl)cyclohexyl]methanol C10H16O 详情 详情
(XIII) 59475 [4-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclohexyl]methanol C14H30O2Si 详情 详情
(XIV) 59476 tert-butyl(dimethyl)silyl [4-(2-propynyl)cyclohexyl]methyl ether; tert-butyl(dimethyl){[4-(2-propynyl)cyclohexyl]methoxy}silane C16H30OSi 详情 详情
(XV) 59477 4-(2-propynyl)cyclohexanecarboxylic acid C10H14O2 详情 详情
(XVI) 59478 methyl 4-(2-propynyl)cyclohexanecarboxylate C11H16O2 详情 详情
Extended Information