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【结 构 式】

【分子编号】41871

【品名】benzhydryl (E)-3-(3-methyl-3-[(2R)-2-methyl-6-[(2R,3R)-4-oxo-3-vinyloxetanyl]hexyl]-2-oxiranyl)-2-butenoate

【CA登记号】

【 分 子 式 】C32H38O5

【 分 子 量 】502.65072

【元素组成】C 76.47% H 7.62% O 15.92%

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 Wittig condensation of aldehyde (XIX) with phosphonium salt (XX) by means of KHMDS in THF/toluene gives the vinyloxirane (XXI), which is treated with diiron nonacarbonyl (XXII) in THF to yield the complex (XXIII). Oxidative decomplexation of (XXIII) with CAN in CH3CN gives the vinyl-beta-lactone (XXIV), which is treated with MCPBA and K2CO3 in CH2Cl2 to yield the epoxide (XXV). The ozonolysis of (XXV), followed by reduction with NaBH4 affords the hydroxymethyl-beta-lactone (XXVI), which is deepoxidated with SmI2 in tert-butanol/THF to provide the protected final intermediate (XXVII). Finally this compound is deprotected with TFA/CH2Cl2.

1 Bates, R.W.; et al.; Total synthesis of the cholesterol biosynthesis inhibitor 1233A via a (Pi-allyl)tricarbonyliron lactone complex. J Chem Soc - Perkins Trans I 1999, 14, 1917.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XIX) 41866 benzhydryl (2E,4E,7R)-11-[(2R,3R)-3-formyloxiranyl]-3,5,7-trimethyl-2,4-undecadienoate C30H36O4 详情 详情
(XX) 41867 (bromomethyl)(triphenyl)phosphorane 1779-49-3 C19H18BrP 详情 详情
(XXI) 41868 benzhydryl (2E,4E,7R)-3,5,7-trimethyl-11-[(2R,3S)-3-vinyloxiranyl]-2,4-undecadienoate C31H38O3 详情 详情
(XXIII) 41869   C33H42O4 详情 详情
(XXIV) 41870 benzhydryl (2E,4E,7R)-3,5,7-trimethyl-11-[(2R,3R)-4-oxo-3-vinyloxetanyl]-2,4-undecadienoate C32H38O4 详情 详情
(XXV) 41871 benzhydryl (E)-3-(3-methyl-3-[(2R)-2-methyl-6-[(2R,3R)-4-oxo-3-vinyloxetanyl]hexyl]-2-oxiranyl)-2-butenoate C32H38O5 详情 详情
(XXVI) 41872 benzhydryl (E)-3-(3-[(2R)-6-[(2R,3R)-3-(hydroxymethyl)-4-oxooxetanyl]-2-methylhexyl]-3-methyl-2-oxiranyl)-2-butenoate C31H38O6 详情 详情
(XXVII) 41873 benzhydryl (2E,4E,7R)-11-[(2R,3R)-3-(hydroxymethyl)-4-oxooxetanyl]-3,5,7-trimethyl-2,4-undecadienoate C31H38O5 详情 详情
Extended Information