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【结 构 式】 
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【分子编号】38214 【品名】 【CA登记号】 |
【 分 子 式 】C69H116N3O15P 【 分 子 量 】1258.665022 【元素组成】C 65.84% H 9.29% N 3.34% O 19.07% P 2.46% |
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)The reaction of the glucopyranosyl bromide (I) (or its chloride analogue) with the N-acyl-L-serinamide (II) by means of Ag-OTf in dichloroethane gives the glucoside (III), which is deprotected at the amino group with Zn and AcOH yielding the 2-aminoglucoside (IV). The condensation of (IV) with the tetradecanoic acid (V) by means of EDDQ in dichloromethane affords the amide (VI), which is finally deprotected by hydrogenation with H2 over PtO2 in THF/AcOH.
| 【1】 Ulrich, J.T.; Keegan, D.S.; Rhodes, M.J.; Johnson, D.A.; Johnson, G.L.; Ward, J.R.; Cantrell, J.L.; Sowell, C.G.; Brookshire, V.G.; Livesay, M.T.; Synthesis and biological evaluation of a new class of vaccine adjuvants: Aminoalkyl glucosaminide 4-phosphates. Bioorg Med Chem Lett 1999, 9, 15, 2273. |
| 【2】 Johnson, D.A.; Sowell, C.G. (Corixa Corp.); Aminoalkyl glucosamine phosphate cpds. and their use as adjuvants and immunoeffectors. EP 0983286; US 6113918; WO 9850399 . |
| 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) | 38211 | (2R,3R,4R,5S,6R)-2-bromo-5-[(diphenoxyphosphoryl)oxy]-6-([[(2,2,2-trichloro-1,1-dimethylethoxy)carbonyl]oxy]methyl)-3-[[(2,2,2-trichloroethoxy)carbonyl]amino]tetrahydro-2H-pyran-4-yl (3R)-3-(decanoyloxy)tetradecanoate | C50H71BrCl6NO14P | 详情 | 详情 | |
| (II) | 38212 | (1R)-1-(2-[[(1S)-2-amino-1-(hydroxymethyl)-2-oxoethyl]amino]-2-oxoethyl)dodecyl decanoate | C27H52N2O5 | 详情 | 详情 | |
| (III) | 38213 | C77H122Cl6N3O19P | 详情 | 详情 | ||
| (IV) | 38214 | C69H116N3O15P | 详情 | 详情 | ||
| (V) | 38215 | (3R)-3-(decanoyloxy)tetradecanoic acid | C24H46O4 | 详情 | 详情 | |
| (VI) | 38216 | C93H160N3O18P | 详情 | 详情 |
Extended Information