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【结 构 式】

【分子编号】65193

【品名】(3aR,4R,5R,6aS)-4-(4,4-difluoro-3-hydroxyoctyl)-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-ol

【CA登记号】

【 分 子 式 】C20H34F2O5

【 分 子 量 】392.4837664

【元素组成】C 61.21% H 8.73% F 9.68% O 20.38%

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:(VIII)

Desilylation of commercial Corey's lactone (I) with TBAF in THF gives carbinol (II), which is oxidized by means of (COCl)2 and DMSO in dichloromethane to yield the carbaldehyde (III). Condensation of compound (III) with phosphonate (IV) by means of thallium ethoxide in dichloromethane affords the unsaturated difluoroketone (V), which is reduced with H2 over Pd/C in ethyl acetate to afford the saturated ketone (VI). Reduction of ketone (VI) with NaBH4 in methanol provides the secondary alcohol (VII), which is further reduced with diisobutylaluminum hydride in toluene to give the lactol (VIII). Condensation of lactol (VIII) with 4-carboxybutyl triphenylphosphonium bromide (IX) by means of t-BuOK in THF yields the prostaglandin F2a derivative (X), which is esterified by means of benzyl bromide and DBU in dichloromethane to afford the benzyl ester (XI). Oxidation of ester (XI) with CrO3 and pyridine in dichloromethane provides the THP-protected prostaglandin E2 derivative (XII), which is treated with AcOH in THF/water to give the prostaglandin E2 benzyl ester derivative (XIII). Finally, this compound is submitted to simultaneous benzyl ester group cleavage and double bond reduction by means of H2 over Pd/C in ethyl acetate.

1 Ueno, R. (R-Tech Ueno, Ltd.); Promotion of wound-healing with 15-keto-prostaglandin cpds.. EP 0503887; US 5252605 .
2 Ueno, R. (R-Tech Ueno, Ltd.); Endothelin antagonist. EP 0978284; US 6197821; WO 9927934 .
3 Sorbera, L.A., Castaner, J., Mealy, N.E.; Lubiprostone. Drugs Fut 2004, 29 (4): 336.
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) 65188 (3aR,4S,5R,6aS)-5-(tetrahydro-2H-pyran-2-yloxy)-4-{[(trimethylsilyl)oxy]methyl}hexahydro-2H-cyclopenta[b]furan-2-one C16H28O5Si 详情 详情
(II) 56988 (3aR,4S,5R,6aS)-4-(hydroxymethyl)-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-one C13H20O5 详情 详情
(III) 56989 (3aR,4R,5R,6aS)-2-oxo-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-4-carbaldehyde C13H18O5 详情 详情
(IV) 65189 dimethyl 3,3-difluoro-2-oxoheptylphosphonate C9H17F2O4P 详情 详情
(V) 65190 (3aR,4R,5R,6aS)-4-[(E)-4,4-difluoro-3-oxo-1-octenyl]-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-one C20H28F2O5 详情 详情
(VI) 65191 (3aR,4R,5R,6aS)-4-(4,4-difluoro-3-oxooctyl)-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-one C20H30F2O5 详情 详情
(VII) 65192 (3aR,4R,5R,6aS)-4-(4,4-difluoro-3-hydroxyoctyl)-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-one C20H32F2O5 详情 详情
(VIII) 65193 (3aR,4R,5R,6aS)-4-(4,4-difluoro-3-hydroxyoctyl)-5-(tetrahydro-2H-pyran-2-yloxy)hexahydro-2H-cyclopenta[b]furan-2-ol C20H34F2O5 详情 详情
(IX) 13616 (4-Carboxybutyl)triphenylphosphonium bromide 17814-85-6 C23H24BrO2P 详情 详情
(X) 65194 (Z)-7-[(1R,2R,3R,5S)-2-(4,4-difluoro-3-hydroxyoctyl)-5-hydroxy-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentyl]-5-heptenoic acid C25H42F2O6 详情 详情
(XI) 65195 benzyl (Z)-7-[(1R,2R,3R,5S)-2-(4,4-difluoro-3-hydroxyoctyl)-5-hydroxy-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentyl]-5-heptenoate C32H48F2O6 详情 详情
(XII) 65196 benzyl (Z)-7-[(1R,2R,3R)-2-(4,4-difluoro-3-oxooctyl)-5-oxo-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentyl]-5-heptenoate C32H44F2O6 详情 详情
(XIII) 65197 benzyl (Z)-7-[(1R,2R,3R)-2-(4,4-difluoro-3-oxooctyl)-3-hydroxy-5-oxocyclopentyl]-5-heptenoate C27H36F2O5 详情 详情
Extended Information