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【结 构 式】

【药物名称】

【化学名称】[1R-(1alpha,3abeta,4beta,5alpha,7aalpha)]-2-[5-[5-Cyano-1-methylene-4(Z)-pentenyl]-1-[1(R),5-dimethylhexyl]-7a-methylperhydroinden-4-yl]acetic acid

【CA登记号】219579-70-1

【 分 子 式 】C27H43NO2

【 分 子 量 】413.64926

【开发单位】Georgia Institute of Technology (Originator), Mayo Clinic (Originator), University of Arizona (Originator)

【药理作用】Oncolytic Drugs, Inhibitors of Signal Transduction Pathways

合成路线1

Ozonolysis of chloesteryl acetate (I) produced keto acid (II), which was converted to the B-homo-6-oxacholestenone (III) upon treatment with SOCl2. Subsequent displacement of the 3beta-acetate group of (III) by NaN3 afforded azide (IV). Pyrolysis of (IV) over silica gel at 180 C yielded a mixture of cleavage products, from which the title nitrile was isolated by column chromatography.

1 Peng, H.; Zalkow, L.H.; Abraham, R.T.; Powis, G.; Novel CDC25A phosphatase inhibitors from pyrolysis of 3-alpha-azido-B-homo-6-oxa-4-cholesten-7-one on silica gel. J Med Chem 1998, 41, 24, 4677.
2 Peng, H.; Zalkow, L.H. (Georgia Technology Research Corp.); Seco-cholestane derivs. and methods of making the same. US 6011058 .
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) 16813 (3S,8S,9S,10R,13R,14S,17R)-17-[(1R)-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate 604-35-3 C29H48O2 详情 详情
(II) 29439 2-[(1R,3aS,4S,5S,7aR)-5-[(1R,4S)-4-(acetoxy)-1-methyl-2-oxocyclohexyl]-1-[(1R)-1,5-dimethylhexyl]-7a-methyloctahydro-1H-inden-4-yl]acetic acid C29H48O5 详情 详情
(III) 29440 (1R,3aS,3bS,8S,10aR,10bS,12aR)-1-[(1R)-1,5-dimethylhexyl]-10a,12a-dimethyl-5-oxo-2,3,3a,3b,4,5,8,9,10,10a,10b,11,12,12a-tetradecahydro-1H-indeno[4,5-d][1]benzoxepin-8-yl acetate C29H46O4 详情 详情
(IV) 29441 (1R,3aS,3bS,8R,10aR,10bS,12aR)-8-azido-1-[(1R)-1,5-dimethylhexyl]-10a,12a-dimethyl-1,2,3,3a,3b,4,8,9,10,10a,10b,11,12,12a-tetradecahydro-5H-indeno[4,5-d][1]benzoxepin-5-one C27H43N3O2 详情 详情
Extended Information