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【结 构 式】

【药物名称】S-17834

【化学名称】6,8-Diallyl-2-(2-allyl-3-hydroxy-4-methoxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one

【CA登记号】178367-40-3

【 分 子 式 】C25H24O6

【 分 子 量 】420.46643

【开发单位】Servier (Originator)

【药理作用】CARDIOVASCULAR DRUGS, Peripheral Vascular Disease, Treatment of, Cell Adhesion Inhibitors, E-Selectin Inhibitors, P-Selectin Inhibitors, VCAM-1 Antagonists

合成路线1

The alkylation of diosmetin (I) with allyl bromide in the presence of NaH in DMF furnished the triallyl ether (II). Claisen rearrangement of (II) in refluxing trichlorobenzene then gave the title compound.

1 Wierzbicki, M.; Boussard, M.-F.; Verbeuren, T.; Vallez, M.-O.; Canet, E.; Rolland, Y. (ADIR et Cie.); Diosmetin derivs., process for their preparation and pharmaceutical compsns. containing them. CA 2161297; EP 0709383; FR 2726273; JP 1996225563; US 5629339 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
11463 3-Bromo-1-propene; 3-Bromopropene;allyl bromide 106-95-6 C3H5Br 详情 详情
(I) 30012 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-chromen-4-one 520-34-3 C16H12O6 详情 详情
(II) 32941 5,7-bis(allyloxy)-2-[3-(allyloxy)-4-methoxyphenyl]-4H-chromen-4-one C25H24O6 详情 详情
Extended Information