【结 构 式】 |
【药物名称】CAM 【化学名称】Ethyl O-[N-(p-carboxyphenyl)carbamoyl]mycophenolate 【CA登记号】40449-96-5 ((E)-isomer) 【 分 子 式 】C27H29NO9 【 分 子 量 】511.53348 |
【开发单位】Ajinomoto (Originator), Chugai (Originator) 【药理作用】IMMUNOMODULATING AGENTS, Immunosuppressants, Oncolytic Drugs |
合成路线1
The reaction of ethyl mycophenolate (I) with phosgene in benzene gives ethyl 5-(4'-chloroformyloxy-6'-methoxy-7'-methyl-3'-oxo-5'-phthalanyl)-3-methyl-3-penten-1-carboxylate (II), which is then condensed with p-aminobenzoic acid (III) in THF.
【1】 Mori, T.; et al.; DE 2237549 . |
【2】 Serradell, M.N.; Castaner, J.; Blancafort, P.; Hillier, K.; CAM. Drugs Fut 1981, 6, 5, 272. |
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) | 37445 | ethyl (E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-2-benzofuran-5-yl)-4-methyl-4-hexenoate | C19H24O6 | 详情 | 详情 | |
(II) | 37446 | ethyl (E)-6-[4-[(chlorocarbonyl)oxy]-6-methoxy-7-methyl-3-oxo-1,3-dihydro-2-benzofuran-5-yl]-4-methyl-4-hexenoate | C20H23ClO7 | 详情 | 详情 | |
(III) | 20004 | p-aminobenzoic acid; 4-aminobenzoic acid | 150-13-0 | C7H7NO2 | 详情 | 详情 |