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【结 构 式】

【分子编号】45070

【品名】4-[((1S)-1-[(1S,3aS,7aS)-4-[(E)-2-((3S,5R)-3,5-bis[[tert-butyl(dimethyl)silyl]oxy]-2-methylenecyclohexylidene)ethylidene]-7a-methyloctahydro-1H-inden-1-yl]ethyl)oxy]-2-methyl-2-butanol

【CA登记号】

【 分 子 式 】C38H70O4Si2

【 分 子 量 】647.1424

【元素组成】C 70.53% H 10.9% O 9.89% Si 8.68%

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:(XXV)

The synthesis of 22-oxacalcitriol labeled with tritium at the 26-methyl group has been performed as follows: The starting compound is the previously obtained 3-oxobutoxy derivative (X), which is submitted to a Grignard alkylation with 3CH3MgI giving the labeled 3-hydroxy-3-methylbutoxy derivative (XXIV). The deprotection of (XXIV) with tetrabutylammonium fluoride affords the triol derivative (XXV), which is finally irradiated with a 400 W high-pressure mercury lamp with a Vycor filter.

1 Leeson, P.A.; Martel, A.M.; Castaner, J.; 22-Oxacalcitriol. Drugs Fut 1996, 21, 12, 1229.
2 Watanabe, H.; Akiyama, M.; Kawanishi, T.; Kubodera, N.; Synthesis of tritiated 1alpha,25-dihydroxy-22-oxavitamin D3. J Label Compd Radiopharm 1995, 36, 7, 645-54.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(X) 11722 4-[[(1S)-1-((1S,3R,9S,10R,13S,14S,17S)-1,3-Bis[[tert-butyl(dimethyl)silyl]oxy]-10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethyl]oxy]-2-butanone C37H66O4Si2 详情 详情
(XXIV) 11723 4-[[(1S)-1-((1S,3R,9S,10R,13S,14S,17S)-1,3-Bis[[tert-butyl(dimethyl)silyl]oxy]-10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethyl]oxy]-2-methyl-2-butanol C38H70O4Si2 详情 详情
(XXIV) 45069 4-[[(1S)-1-((1S,3R,9S,10R,13S,14S,17S)-1,3-bis[[tert-butyl(dimethyl)silyl]oxy]-10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethyl]oxy]-2-methyl-2-butanol C38H70O4Si2 详情 详情
(XXV) 11733 (1S,3R,9S,10R,13S,14S,17S)-17-[(1S)-1-(3-Hydroxy-3-methylbutoxy)ethyl]-10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-1,3-diol C26H42O4 详情 详情
(XXV) 45070 4-[((1S)-1-[(1S,3aS,7aS)-4-[(E)-2-((3S,5R)-3,5-bis[[tert-butyl(dimethyl)silyl]oxy]-2-methylenecyclohexylidene)ethylidene]-7a-methyloctahydro-1H-inden-1-yl]ethyl)oxy]-2-methyl-2-butanol C38H70O4Si2 详情 详情
Extended Information