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【结 构 式】

【分子编号】30520

【品名】[6-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-2-(4-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]phenyl)-1-benzothiophen-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone

【CA登记号】

【 分 子 式 】C34H39NO4S3

【 分 子 量 】621.886

【元素组成】C 65.67% H 6.32% N 2.25% O 10.29% S 15.47%

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)

Keoxifene has been synthesized using the following process: A portion of 6-methanesulfonyloxy-2-(4-methanesulfonyloxyphenyl)-3-[4-(2-pipendinoethoxy)benzoyl]benzo[b]thiophene hydrochloride (I) was combined with denatured alcohol and 5N sodium hydroxide, and stirred under a nitrogen atmosphere. The reaction mixture was evaporated to dryness under vacuum, and the residue dissolved in water and washed with diethyl ether. The water layer was degassed under vacuum, and then nitrogen was bubbled through it to remove all traces of ether. The mixture was then acidified with 1N hydrochloric acid, and then made basic with excess sodium bicarbonate The precipitate was collected by filtration and washed with cold water to obtain crude product, which was purified on a column of silica gel. The column was eluted first with 700 ml of 5% methanol in chloroform, followed by 1l of 10% methanol in chloroform. The impurities came off first, and the product-containing fractions were combined and evaporated under vacuum to obtain a yellow oil. The oil was dissolved in acetone seeded and chilled in a freezer to obtain the purified product.

1 Peters, M.K.; Jones, C.D.; Benzothiophene compounds and process for preparing them. EP 0062053; GB 2097788 .
2 Pento, J.T.; Keoxifene. Drugs Fut 1984, 9, 7, 516.
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) 30520 [6-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-2-(4-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]phenyl)-1-benzothiophen-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone C34H39NO4S3 详情 详情
(II) 17321 [6-hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl][4-(2-piperidinoethoxy)phenyl]methanone C28H27NO4S 详情 详情
Extended Information