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【结 构 式】

【分子编号】58152

【品名】 

【CA登记号】

【 分 子 式 】C86H144O46

【 分 子 量 】1914.06176

【元素组成】C 53.97% H 7.58% O 38.45%

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:(XXI)

The nonasaccharide (XX) is transformed into (XXI) by the sequence of benzoate esters hydrolysis, O-methylation, acetal hydrolysis, and selective mono-benzoylation, following the same methods as above. The free hydroxyl group of (XXI) is subsequently protected by esterification with levulinic acid (XXII) to give levulinate ester (XXIII). Opening of the 1,6-anhydroglucose unit of (XXIII) is then accomplished by treatment with acetic anhydride in the presence of acetic acid and trifluoroacetic acid, producing (XXIV).

1 Petitou, M.; Herbert, J.-M.; Duchaussoy, P.; Basten, J.; Dreef-Tromp, C.; Driguez, P.-A.; Van Boeckel, C. (Akzo Nobel N.V.; Sanofi-Synthélabo); Synthetic polysaccharides, their method of production and pharmaceutical compsns. containing same. EP 1049721; FR 2773804; US 6528497; WO 9936443 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XX) 58151   C122H156O51 详情 详情
(XXI) 58152   C86H144O46 详情 详情
(XXII) 36170 4-oxopentanoic acid 123-76-2 C5H8O3 详情 详情
(XXIII) 58153   C91H150O48 详情 详情
(XXIV) 58154   C95H156O51 详情 详情
Extended Information