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【结 构 式】

【分子编号】59319

【品名】5-{acetyl[2-(acetyloxy)-3-methoxypropyl]amino}-2,4,6-triiodoisophthalic acid

【CA登记号】

【 分 子 式 】C16H16I3NO8

【 分 子 量 】731.01839

【元素组成】C 26.29% H 2.21% I 52.08% N 1.92% O 17.51%

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)

Alternatively, 5-acetamido-2,4,6-triiodoisophthalic acid (I) is alkylated with 1-chloro-3-methoxy-2-propanol (II) to produce (III). After protection of the alcoholic hydroxyl group as the acetate ester (IV), the carboxyl groups are activated as the corresponding acid chloride (V) with SOCl2. Coupling of (V) with 3-amino-1,2-propanediol (VI) then produces the title amide.

1 Skjoeld, W.; Berg, A.; Preparative liquid chromatography in the field of X-ray contrast agents. J Chromatogr 1986, 366, 299.
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) 59317 5-(acetylamino)-2,4,6-triiodoisophthalic acid C10H6I3NO5 详情 详情
(II) 34214 1-chloro-3-methoxy-2-propanol 4151-97-7 C4H9ClO2 详情 详情
(III) 59318 5-[acetyl(2-hydroxy-3-methoxypropyl)amino]-2,4,6-triiodoisophthalic acid C14H14I3NO7 详情 详情
(IV) 59319 5-{acetyl[2-(acetyloxy)-3-methoxypropyl]amino}-2,4,6-triiodoisophthalic acid C16H16I3NO8 详情 详情
(V) 59320 2-[acetyl-3,5-bis(chlorocarbonyl)-2,4,6-triiodoanilino]-1-(methoxymethyl)ethyl acetate C16H14Cl2I3NO6 详情 详情
(VI) 12979 3-Amino-1,2-propanediol;3-aminopropane-1,2-diol 616-30-8 C3H9NO2 详情 详情
Extended Information