【结 构 式】 |
【分子编号】64638 【品名】(2R,3S,4S)-4-(1,3-dithian-2-yl)-2-methyl-1,3-pentanediol 【CA登记号】 |
【 分 子 式 】C10H20O2S2 【 分 子 量 】236.3996 【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:(LI)Dithiane intermediate (LII). The ozonolysis of the allylic diol (XLVIII) with O3 and PPh3 in dichloromethane/methanol gives the aldehyde (XLIX), which is condensed with propane-1,3-dithiol (L) by means of BF3/OEt2 in dichloromethane to yield the dihydroxylated 1,3-dithiane derivative (LI). Finally, this compound is protected with 3,4-Dmp-CHO (A) and PPTS to afford the desired dithiane intermediate (LII).
【1】 Smith, A.B.; et al.; The spongistatins: Architecturally complex natural products - Part one: A formal synthesis of (+)-spongistatin 1 by construction of an advanced ABCD fragment. Angew Chem. Int Ed 2001, 40, 1, 191. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(A) | 46036 | 3,4-dimethylbenzaldehyde | 5973-71-7 | C9H10O | 详情 | 详情 |
(XVIII) | 64636 | (2R,3R,4R)-1-{[tert-butyl(dimethyl)silyl]oxy}-2,4-dimethyl-5-hexen-3-ol | C14H30O2Si | 详情 | 详情 | |
(XLIX) | 64637 | (2S,3S,4R)-5-{[tert-butyl(dimethyl)silyl]oxy}-3-hydroxy-2,4-dimethylpentanal | C13H28O3Si | 详情 | 详情 | |
(L) | 29729 | 1,3-propanedithiol; 3-sulfanylpropylhydrosulfide | 109-80-8 | C3H8S2 | 详情 | 详情 |
(LI) | 64638 | (2R,3S,4S)-4-(1,3-dithian-2-yl)-2-methyl-1,3-pentanediol | C10H20O2S2 | 详情 | 详情 | |
(LII) | 64639 | (4S,5R)-2-(3,4-dimethylphenyl)-4-[(1S)-1-(1,3-dithian-2-yl)ethyl]-5-methyl-1,3-dioxane | C19H28O2S2 | 详情 | 详情 |
Extended Information