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【结 构 式】

【药物名称】Sanazole, AK-2123

【化学名称】2-(3-Nitro-1,2,4-triazol-1-yl)-N-(2-methoxyethyl)acetamide
      N-(2-Methoxyethyl)-2-(3-nitro-1,2,4-triazol-1-yl)acetamide

【CA登记号】104958-90-9

【 分 子 式 】C7H11N5O4

【 分 子 量 】229.19682

【开发单位】Adeka Fine Chem. (Originator), Kyoto University (Originator)

【药理作用】ONCOLYTIC DRUGS, Radiation Therapy, Radiosensitizers

合成路线1

Condensation of aminoguanidine carbonate (I) with formic acid gives 3-aminotriazole (II), which by treatment with concentrated nitric acid in a sodium nitrite solution gives 3-nitrotriazole (III). N-Alkylation of (III) with bromoacetic acid ethyl ester affords 2-(3-nitro-1,2,4-triazol-1-yl)acetic acid ethyl ester (IV). Reaction of (IV) with 2-methoxyethylamine in dioxane yields AK-2123.

1 Horning, E.C.; Organic Syntheses, Vol. 3, 1st Ed. University of Missouri 1995, 95.
2 Sugita, T.; Masuoka, M.; Nishikawa, Y.; Nishimoto, S.; Zhuo, L.; Sasai, K.; Kagiya, T.; Nitrotriazoles bearing sulfur-substituted side chains: Preparation and characterization as hypoxic cell radiosensitizers. Anti-Cancer Drug Des 1992, 7, 277-84.
3 Huan, L.C.; Rong, S.; AK-2123. Drugs Fut 1995, 20, 7, 659.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
16640 Ethyl 2-bromoacetate; Ethyl bromoacetate 105-36-2 C4H7BrO2 详情 详情
34675 2-methoxyethylamine; 2-methoxy-1-ethanamine 109-85-3 C3H9NO 详情 详情
(I) 10015 1-Hydrazinecarboximidamide; Hydrazinecarboximidamide 79-17-4 CH6N4 详情 详情
(II) 12475 1H-1,2,4-Triazol-3-amine; 1H-1,2,4-Triazol-3-ylamine 61-82-5 C2H4N4 详情 详情
(III) 12476 3-Nitro-1H-1,2,4-triazole; 3-Nitro-1,2,4-triazole 24807-55-4 C2H2N4O2 详情 详情
(IV) 12477 ethyl 2-(3-nitro-1H-1,2,4-triazol-1-yl)acetate C6H8N4O4 详情 详情
Extended Information