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【结 构 式】

【分子编号】50026

【品名】2-[dimethyl(phenyl)silyl]ethyl (2S)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-[2-(3-methyl-2-butenyl)-1H-indol-3-yl]propanoate

【CA登记号】

【 分 子 式 】C34H36N2O4Si

【 分 子 量 】564.75642

【元素组成】C 72.31% H 6.43% N 4.96% O 11.33% Si 4.97%

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:(III)

The esterification of the silylated resin (II) with the prenyltryptophan derivative (I) by means of HATU, OBT and DIEA in DMF gives the resin-bonded ester (III), which is treated with hydrazine in methanol/dichloromethane to eliminate the protecting phthalimido group and yield the resin-bonded tryptophan ester derivative (IV). The condensation of (IV) with N-(Fmoc)-L-proline (V) by means of HATU, HOBT and DIEA in DMF affords the dipeptide (VI), which is treated with piperidine in N-methylpyrrolidine to eliminate the Fmoc protecting group and yield dipeptide ester (VII). Finally, this compound is submitted to an acid-induced cyclization by means of HOAc in refluxing methanol to afford the target bicyclic diketopiperazine.

1 Wang, B.B.; et al.; Preparation of novel 2-(trialkylsilyl)ethyl linkers and first synthesis of Tryprostatin B on solid phase. Tetrahedron Lett 2001, 42, 8, 1463.
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) 50024 (2S)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-[2-(3-methyl-2-butenyl)-1H-indol-3-yl]propionic acid C24H22N2O4 详情 详情
(II) 50025 2-[dimethyl(phenyl)silyl]-1-ethanol C10H16OSi 详情 详情
(III) 50026 2-[dimethyl(phenyl)silyl]ethyl (2S)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-[2-(3-methyl-2-butenyl)-1H-indol-3-yl]propanoate C34H36N2O4Si 详情 详情
(IV) 50027 2-[dimethyl(phenyl)silyl]ethyl (2S)-2-amino-3-[2-(3-methyl-2-butenyl)-1H-indol-3-yl]propanoate C26H34N2O2Si 详情 详情
(V) 34762 (2S)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-pyrrolidinecarboxylic acid 71989-31-6 C20H19NO4 详情 详情
(VI) 50028 9H-fluoren-9-ylmethyl (2S)-2-[[((1S)-2-[2-[dimethyl(phenyl)silyl]ethoxy]-1-[[2-(3-methyl-2-butenyl)-1H-indol-3-yl]methyl]-2-oxoethyl)amino]carbonyl]-1-pyrrolidinecarboxylate C46H51N3O5Si 详情 详情
(VII) 50029 2-[dimethyl(phenyl)silyl]ethyl (2S)-3-[2-(3-methyl-2-butenyl)-1H-indol-3-yl]-2-[[(2S)pyrrolidinylcarbonyl]amino]propanoate C31H41N3O3Si 详情 详情
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