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【结 构 式】

【分子编号】34698

【品名】isopropyl (Z)-7-[(1R,2R,3R,5R)-2-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-5-formyl-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentyl]-5-heptenoate

【CA登记号】

【 分 子 式 】C35H64O6Si

【 分 子 量 】608.97506

【元素组成】C 69.03% H 10.59% O 15.76% Si 4.61%

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:(X)

The title compound was synthesized starting from the described intermediate (I). Hydrogenation of the olefinic double bond in the presence of PtO2 afforded (II). After protection of the free hydroxyl group of (II) as the corresponding silyl ether (III) with tert-butyldimethylsilyl chloride and imidazole, hydrolysis of the acetate ester of (III) by means of K2CO3 in MeOH furnished alcohol (IV). Further protection of (IV) employing dihydropyran and camphorsulfonic acid gave tetrahydropyranyl ether (V). Reduction of the lactone function of (V) with DIBAL in toluene at -78 C produced lactol (VI), which was submitted to a Wittig reaction with the ylide resulting from phosphonium salt (VII) and t-BuOK to yield the cis olefin (VIII). Esterification of (VIII) with isopropanol in the presence of 2-chloro-1-methylpyridinium iodide gave isopropyl ester (IX). Inversion of the configuration of the 9beta-hydroxyl group of (IX) was then achieved by Mitsunobu coupling with formic acid to give the 9beta-formate ester (X). Subsequent hydrolysis of the formate ester of (X) with K2CO3 in hot isopropanol, followed by acid deprotection of the tetrahydropyranyl and silyl groups yielded the title compound.

1 Miyazaki, T.; Kawakura, M.; Shirasawa, E. (Ono Pharmaceutical Co., Ltd.); 13,14-Dihydro-PGF2BETA and its isopropyl ester. CA 2125804; EP 0628545; JP 1995061965 .
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) 34696 2-chloro-1-methylpyridinium iodide 14338-32-0 C6H7ClIN 详情 详情
(I) 34689 (3aR,4R,5R,6aS)-4-[(E,3S)-3-hydroxy-1-octenyl]-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl acetate C17H26O5 详情 详情
(II) 34690 (3aR,4R,5R,6aS)-4-[(3S)-3-hydroxyoctyl]-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl acetate C17H28O5 详情 详情
(III) 34691 (3aR,4R,5R,6aS)-4-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-2-oxohexahydro-2H-cyclopenta[b]furan-5-yl acetate C23H42O5Si 详情 详情
(IV) 34692 (3aR,4R,5R,6aS)-4-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-5-hydroxyhexahydro-2H-cyclopenta[b]furan-2-one C21H40O4Si 详情 详情
(V) 34693 (3aR,4R,5R,6aS)-4-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-one C26H48O5Si 详情 详情
(VI) 34694 (3aR,4R,5R,6aS)-4-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-ol C26H50O5Si 详情 详情
(VII) 13616 (4-Carboxybutyl)triphenylphosphonium bromide 17814-85-6 C23H24BrO2P 详情 详情
(VIII) 34695 (Z)-7-[(1R,2R,3R,5S)-2-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-5-hydroxy-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentyl]-5-heptenoic acid C31H58O6Si 详情 详情
(IX) 34697 isopropyl (Z)-7-[(1R,2R,3R,5S)-2-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-5-hydroxy-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentyl]-5-heptenoate C34H64O6Si 详情 详情
(X) 34698 isopropyl (Z)-7-[(1R,2R,3R,5R)-2-((3S)-3-[[tert-butyl(dimethyl)silyl]oxy]octyl)-5-formyl-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentyl]-5-heptenoate C35H64O6Si 详情 详情
Extended Information