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【结 构 式】

【分子编号】42779

【品名】methyl (2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-hydroxytetrahydro-2H-pyran-2-carboxylate

【CA登记号】

【 分 子 式 】C13H18O10

【 分 子 量 】334.27992

【元素组成】C 46.71% H 5.43% O 47.86%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(I)

By condensation of D-glucopyranuronic acid methyl ester (I) with (3R,4S)-3-[3-acetoxy-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-(4-hydroxyphenyl)azetidin-2-one (III) by means of Tms-OTf.

1 Taraporewala, I.B.; Kauffman, J.M.; Synthesis and structure activity relationships of anti-inflammatory 9,10-dihydro-9-oxo-2-acridine-alkanoic acids and 4-(2-carboxyphenyl)aminobenzenealkanoic acids. J Pharm Sci 1990, 79, 2, 173.
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) 42779 methyl (2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-hydroxytetrahydro-2H-pyran-2-carboxylate C13H18O10 详情 详情
(II) 42780 (trimethylsilyl)[(2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl]oxonium trifluoromethanesulfonate C17H27F3O13SSi 详情 详情
(III) 42152 (1S)-1-(4-fluorophenyl)-3-[(2S,3R)-1-(4-fluorophenyl)-2-(4-hydroxyphenyl)-4-oxoazetidinyl]propyl acetate C26H23F2NO4 详情 详情

合成路线2

该中间体在本合成路线中的序号:(I)

By condensation of D-glucopyranuronic acid methyl ester (I) with 3-butyl-3-ethyl-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-ol S,S-dioxide (III) by means of Tms-OTf.

1 Walker, E.H.; Palomino, E.; Blumenthal, S.L.; Carbohydrate prodrugs: potential use for in situ activation and drug delivery. Drugs Fut 1991, 16, 11, 1029.
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) 42779 methyl (2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-hydroxytetrahydro-2H-pyran-2-carboxylate C13H18O10 详情 详情
(II) 42780 (trimethylsilyl)[(2S,3R,4S,5R,6S)-3,4,5-tris(acetoxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl]oxonium trifluoromethanesulfonate C17H27F3O13SSi 详情 详情
(III) 42781 3-butyl-3-ethyl-8-hydroxy-5-phenyl-2,3,4,5-tetrahydro-1H-1lambda(6),4-benzothiazepine-1,1-dione C21H27NO3S 详情 详情
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