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【结 构 式】

【分子编号】54153

【品名】vmethyl (2S,3S,4S,5R,6R)-6-({(2R,3S,4R,5R,6S)-4,5-bis(benzyloxy)-2-[(benzyloxy)methyl]-6-methoxytetrahydro-2H-pyran-3-yl}oxy)-3-hydroxy-4,5-dimethoxytetrahydro-2H-pyran-2-carboxylate

【CA登记号】n/a

【 分 子 式 】C37H46O12

【 分 子 量 】682.76504

【元素组成】C 65.09% H 6.79% O 28.12%

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:(XIII)

The L-ioduronic acid methyl ester derivative (XII) is then converted into its D-glucuronic acid methyl ester counterpart (XIII) by epimerization with NaOMe in refluxing MeOH, followed by esterification with MeI and KHCO3 in DMF. Protection of the ester (XIII) with levulinic acid (IX) by means of DCC and DMAP in dioxane, followed by acetolysis of the anomeric center with sulfuric acid in acetic anhydride furnishes the disaccharide (XIV), which is then saponified with piperidine and subjected to reaction with trichloroacetonitrile and Cs2CO3 in THF to yield the imidate (XV). Glycosylation of the disaccharide (XII) with the imidate (XV) by means of trimethylsilyl triflate in CH2Cl2, followed by removal of the levulinoyl group by means of hydrazine acetate, furnishes the tetrasaccharide (XVI), which is coupled with the glucosyl trichloroacetimidate (XVIII) by means of trimethylsilyl trifluoromethanesulfonate in CH2Cl2 providing the pentasaccharide (XVII). Glucosyl imidate (XVIII) is prepared by methylation of 1,6-anhydroglucose (XIX) with MeI and NaH in DMF, followed by acetolysis with Ac2O/TFA to give compound (XX), which is treated with piperidine in THF and finally with trichloroacetonitrile in dichloromethane in the presence of Cs2CO3. The pentasaccharide (XVII) is deprotected by saponification with LiOH in THF/H2O2, and then hydrogenated over Pd/C in tert-butanol/water to provide a fully deprotected pentamer, which is finally subjected to sulfation with triethylamine sulfur trioxide complex in DMF and converted into the corresponding sodium salt by elution in a Dowex 50 XW4-Na+ or a Mono-Q anion-exchange column.

1 del Fresno, M.; Diaz-Ricart, M.; Idraparinux Sodium. Drugs Fut 2002, 27, 7, 639.
2 Basten, J.E.M.; van Boeckel, C.A.A.; Westerduin, P.; et al.; Feasible synthesis and biological properties of six "non-glycosamino" glycan analogues of the antithrombin III binding heparin pentasaccharide. Bioorg Med Chem 1994, 2, 11, 1267.
3 van Boeckel, C.A.A.; Petitou, M. (Akzo Nobel N.V.; Sanofi-Synthelabo); Carbohydrate derivs. comprising a trisaccharide unit. EP 0454220; JP 1992225994; US 5378829; US 5382570; US 5529985; US 5773605 .
4 Petitou, M.; van Boeckel, C.A.A. (Akzo Nobel N.V.; Sanofi-Synthelabo); Sulfated glycosaminoglycanoid derivs.. EP 0529715 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 36170 4-oxopentanoic acid 123-76-2 C5H8O3 详情 详情
(XII) 54152 methyl (2R,3S,4S,5R,6R)-6-({(2R,3S,4R,5R,6S)-4,5-bis(benzyloxy)-2-[(benzyloxy)methyl]-6-methoxytetrahydro-2H-pyran-3-yl}oxy)-3-hydroxy-4,5-dimethoxytetrahydro-2H-pyran-2-carboxylate n/a C37H46O12 详情 详情
(XIII) 54153 vmethyl (2S,3S,4S,5R,6R)-6-({(2R,3S,4R,5R,6S)-4,5-bis(benzyloxy)-2-[(benzyloxy)methyl]-6-methoxytetrahydro-2H-pyran-3-yl}oxy)-3-hydroxy-4,5-dimethoxytetrahydro-2H-pyran-2-carboxylate n/a C37H46O12 详情 详情
(XIV) 54154 methyl (2S,3S,4R,5R,6R)-6-{[(2R,3R,4R,5R)-4,6-bis(acetyloxy)-2-[(acetyloxy)methyl]-5-(benzyloxy)tetrahydro-2H-pyran-3-yl]oxy}-4,5-dimethoxy-3-[(4-oxopentanoyl)oxy]tetrahydro-2H-pyran-2-carboxylate n/a C33H44O17 详情 详情
(XV) 54155 methyl (2S,3S,4R,5R,6R)-6-({(2R,3R,4R,5R)-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(benzyloxy)-6-[(2,2,2-trichloroethanimidoyl)oxy]tetrahydro-2H-pyran-3-yl}oxy)-4,5-dimethoxy-3-[(4-oxopentanoyl)oxy]tetrahydro-2H-pyran-2-carboxylate n/a C33H42Cl3NO16 详情 详情
(XVI) 54156 methyl (2S,3S,4S,5R,6R)-6-[((2R,3R,4R,5R,6S)-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(benzyloxy)-6-{[(2R,3S,4R,5R,6R)-6-({(2R,3S,4R,5R,6S)-4,5-bis(benzyloxy)-2-[(benzyloxy)methyl]-6-methoxytetrahydro-2H-pyran-3-yl}oxy)-4,5-dimethoxy-2-(methoxycarbonyl n/a C63H80O25 详情 详情
(XVII) 54158   n/a C74H98O31 详情 详情
(XVIII) 54157 {(2R,3S,4S,5R,6R)-3,4,5-trimethoxy-6-[(2,2,2-trichloroethanimidoyl)oxy]tetrahydro-2H-pyran-2-yl}methyl acetate n/a C13H20Cl3NO7 详情 详情
(XIX) 54159 (1R,2S,3S,4R,5R)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol n/a C6H10O5 详情 详情
(XX) 54160 (3R,4S,5S,6R)-6-[(acetyloxy)methyl]-3,4,5-trimethoxytetrahydro-2H-pyran-2-yl acetate n/a C13H22O8 详情 详情
Extended Information