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【结 构 式】

【分子编号】29071

【品名】(2R,3S,4R)-3-[(E)-4-methyl-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-1-octenyl]-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-2-[8-(tetrahydro-2H-pyran-2-yloxy)octyl]cyclopentanone

【CA登记号】

【 分 子 式 】C39H68O7

【 分 子 量 】648.96472

【元素组成】C 72.18% H 10.56% O 17.26%

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:(IX)

The Grignard reaction of propargylmagnesium bromide (I) with 2-hexanone (II) in ether gives 4-methyloct-1-in-4-ol (III), which by reaction with diisobutylaluminum hydride and I2 is converted to 1-iodo-4-methyloct-1-en-4-ol (IV). The reaction of (IV) with dihydropyran and p-toluenesulfonic acid yields the corresponding tetrahydropyranyloxy derivative (V), which by reaction with tert-butyllithium and copper pentyne (VI) affords the corresponding organolithiocuprate (VII). The condensation of (VII) with 4R-(tetrahydropyranyloxy)-2-[7-(tetrahydropyranyloxyl)heptyl]cyclopent-2-en-1-one (VIII) in ether gives 1,11,16-tris(tetrahydropyranyloxy)-16-methylprost-13-en-9-one (IX), which is finally deprotected by a treatment with acetic acid in water THF.

1 Woessner, W.D.; Biddlecom, W.G.; Kluender, H.C. (Bayer Corp.); Preparation of 15-deoxy-16-hydroxyprostaglandins. US 4132738 .
2 Castaner, J.; Serradell, M.N.; Rioprostil. Drugs Fut 1985, 10, 3, 207.
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) 29064 bromo(2-propynyl)magnesium C3H3BrMg 详情 详情
(II) 29065 2-hexanone 591-78-6 C6H12O 详情 详情
(III) 29066 4-methyl-1-octyn-4-ol C9H16O 详情 详情
(IV) 29067 (E)-1-iodo-4-methyl-1-octen-4-ol C9H17IO 详情 详情
(V) 29068 (E)-2-butyl-5-iodo-2-methyl-4-pentenyl tetrahydro-2H-pyran-2-yl ether C15H27IO2 详情 详情
(VI) 29069 1-pentynylcopper C5H7Cu 详情 详情
(VIII) 29070 (4R)-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-2-[8-(tetrahydro-2H-pyran-2-yloxy)octyl]-2-cyclopenten-1-one C24H40O5 详情 详情
(IX) 29071 (2R,3S,4R)-3-[(E)-4-methyl-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-1-octenyl]-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-2-[8-(tetrahydro-2H-pyran-2-yloxy)octyl]cyclopentanone C39H68O7 详情 详情
Extended Information