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【结 构 式】

【分子编号】25345

【品名】(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4-(acetoxy)-12-[[(E)-3-(3-benzoylphenyl)-2-propenoyl]oxy]-1,15-dihydroxy-10,14,17,17-tetramethyl-11-oxo-9-[(triethylsilyl)oxy]-6-oxatetracyclo[11.3.1.0(3,10).0(4,7)]heptadec-13-en-2-yl benzoate

【CA登记号】

【 分 子 式 】C51H60O12Si

【 分 子 量 】893.1157

【元素组成】C 68.59% H 6.77% O 21.5% Si 3.14%

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:(IV)

Selective protection of the 7-hydroxyl group of deacetylbaccatin (I) with triethylsilyl chloride provided silyl ether (II), which was acylated at position 10 with the activated ester (III) in the presence of lithium hexamethyldisilazide to give the benzoylcinnamic ester (IV). Further coupling of (IV) with beta-lactam (V) gave (VI), which by removal of the silyl groups with HF in pyridine-acetonitrile afforded (VII). The Boc group of (VII) was then removed with trifluoroacetic acid to give amine (VIII).

1 Ahern, D.G.; Ojima, I.; Bounaud, P.-Y.; New photoaffinity analogs of paclitaxel. Bioorg Med Chem Lett 1999, 9, 8, 1189.
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) 25331 3-hydroxyacetophenone; 1-(3-hydroxyphenyl)-1-ethanone 121-71-1 C8H8O2 详情 详情
(II) 25341 3-(3,4-dimethoxyphenyl)-1-(3-hydroxyphenyl)-1-propanone C17H18O4 详情 详情
(III) 25344 2-[[(E)-3-(3-benzoylphenyl)-2-propenoyl]oxy]-1H-isoindole-1,3(2H)-dione C24H15NO5 详情 详情
(IV) 25345 (1S,2S,3R,4S,7R,9S,10S,12R,15S)-4-(acetoxy)-12-[[(E)-3-(3-benzoylphenyl)-2-propenoyl]oxy]-1,15-dihydroxy-10,14,17,17-tetramethyl-11-oxo-9-[(triethylsilyl)oxy]-6-oxatetracyclo[11.3.1.0(3,10).0(4,7)]heptadec-13-en-2-yl benzoate C51H60O12Si 详情 详情
(V) 25333 tert-butyl (3R,4S)-2-oxo-4-phenyl-3-[(triisopropylsilyl)oxy]-1-azetidinecarboxylate C23H37NO4Si 详情 详情
(VI) 25346 (1S,2S,3R,4S,7R,9S,10S,12R,15S)-4-(acetoxy)-12-[[(E)-3-(3-benzoylphenyl)-2-propenoyl]oxy]-15-([(2R,3S)-3-[(tert-butoxycarbonyl)amino]-3-phenyl-2-[(triisopropylsilyl)oxy]propanoyl]oxy)-1-hydroxy-10,14,17,17-tetramethyl-11-oxo-9-[(triethylsilyl)oxy] C74H97NO16Si2 详情 详情
(VII) 25347 (1S,2S,3R,4S,7R,9S,10S,12R,15S)-4-(acetoxy)-12-[[(E)-3-(3-benzoylphenyl)-2-propenoyl]oxy]-15-([(2R,3S)-3-[(tert-butoxycarbonyl)amino]-2-hydroxy-3-phenylpropanoyl]oxy)-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.0(3,10).0(4, C59H63NO16 详情 详情
(VIII) 25382 (1S,2S,3R,4S,7R,9S,10S,12R,15S)-4-(acetoxy)-15-[[(2R,3S)-3-amino-2-hydroxy-3-phenylpropanoyl]oxy]-12-[[(E)-3-(3-benzoylphenyl)-2-propenoyl]oxy]-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.0(3,10).0(4,7)]heptadec-13-en-2-yl C54H55NO14 详情 详情
Extended Information