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【结 构 式】

【分子编号】25717

【品名】(2S,3R)-3-[[tert-butyl(dimethyl)silyl]oxy]-2-methyldecanoic acid

【CA登记号】

【 分 子 式 】C17H36O3Si

【 分 子 量 】316.55654

【元素组成】C 64.5% H 11.46% O 15.16% Si 8.87%

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:(V)

Boron enolate obtained from chiral propionyloxazolidinone (I) and dibutylboron triflate (Bu2BOTf) was condensed with n-octanal (II) to produce the syn aldol compound (III), which was protected as the silyl ether (IV) with tert-butyldimethylsilyl triflate. Then, removal of the chiral auxiliary by hydrolysis with lithium peroxide afforded the (2S,3R)-beta-(silyloxy)acid (V). After activation as the mixed anhydride (VII) with 2,4,6-trichlorobenzoyl chloride (VI), esterification with benzyl (S)-2-hydroxy-3-methylbutyrate (VIII) gave diester (IX). Subsequent removal of the silyl group using HF in acetonitrile provided intermediate (X).

1 Wagner, B.; et al.; Total synthesis and conformational studies of hapalosin, N-desmethylhapalosin and 8-deoxyhapalosin. Bioorg Med Chem 1999, 7, 5, 737.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
40666 tert-butyl(dimethyl)silyl trifluoromethanesulfonoperoxoate C7H15F3O4SSi 详情 详情
(I) 25713 (4S)-4-benzyl-3-propionyl-1,3-oxazolidin-2-one C13H15NO3 详情 详情
(II) 25714 octanal 124-13-0 C8H16O 详情 详情
(III) 25715 (4S)-4-benzyl-3-[(2S,3R)-3-hydroxy-2-methyldecanoyl]-1,3-oxazolidin-2-one C21H31NO4 详情 详情
(IV) 25716 (4S)-4-benzyl-3-((2S,3R)-3-[[tert-butyl(dimethyl)silyl]oxy]-2-methyldecanoyl)-1,3-oxazolidin-2-one C27H45NO4Si 详情 详情
(V) 25717 (2S,3R)-3-[[tert-butyl(dimethyl)silyl]oxy]-2-methyldecanoic acid C17H36O3Si 详情 详情
(VI) 25718 2,4,6-trichlorobenzoyl chloride 4136-95-2 C7H2Cl4O 详情 详情
(VII) 25719 (2S,3R)-2-[[tert-butyl(dimethyl)silyl]oxy]-1-methyldecanoic 2,4,6-trichloro-1-benzenecarboxylic anhydride C24H37Cl3O4Si 详情 详情
(VIII) 25720 benzyl (2S)-2-hydroxy-3-methylbutanoate C12H16O3 详情 详情
(IX) 25721 (1S)-1-[(benzyloxy)carbonyl]-2-methylpropyl (2S,3R)-3-[[tert-butyl(dimethyl)silyl]oxy]-2-methyldecanoate C29H50O5Si 详情 详情
(X) 25722 (1S)-1-[(benzyloxy)carbonyl]-2-methylpropyl (2S,3R)-3-hydroxy-2-methyldecanoate C23H36O5 详情 详情
Extended Information