【结 构 式】 |
【药物名称】Elmustine, NSC-29485, HECNU 【化学名称】1-(2-Chloroethyl)-3-(2-hydroxyethyl)nitrosourea 【CA登记号】60784-46-5 【 分 子 式 】C5H10ClN3O3 【 分 子 量 】195.60675 |
【开发单位】Asta Medica (Originator), Degussa (Licensee) 【药理作用】ONCOLYTIC DRUGS, DNA-Damaging Drugs |
合成路线1
HECNU can be prepared as follows (2): The reaction of 2-chloroethylisocyanate (I) with activated sodium azide yields 2-chloroethylcarbamoylazide (II). The preparation of N-(2-chloroethyl)-N-nitrosocarbamoylazide (III) was performed by adding 2-chloroethylcarbamoyiazide (III) to a suspension of anhydrous sodium acetate and nitrogen tetroxide in carbon tetrachloride. Reaction of N-(2-chloroethyl)-N-nitrosocarbamoylazide (III) with ethanolamine (IV) in isopropanol yields elmustine. The described synthetic approach offers a useful means to get the nitroso group attached to the required position.
【1】 Eisenbrand, G.; et al.; Some new congeners of the anticancer 1,2-bis(2-chloroethyl)-1-nitrosourea (BCNU). Synthesis of bifunctional analogs and water soluble derivatives and preliminary evaluation of their chemotherapeutic potential. Z Krebsforsch 1976, 86, 279. |
【2】 Hansch, C.; et al.; Quantitative structure activity relationships of antineoplastic drugs: Nitrosoureas and triazenoimidazoles. Cancer Chemother Rep 1972, 56, 443. |
【3】 Castaner, J.; Serradell, M.N.; Elmustine. Drugs Fut 1984, 9, 1, 18. |
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) | 11237 | 1-Chloro-2-isocyanatoethane; 2-Chloroethyl isocyanate | 1943-83-5 | C3H4ClNO | 详情 | 详情 |
(II) | 29946 | 1-[(azidocarbonyl)amino]-2-chloroethane | C3H5ClN4O | 详情 | 详情 | |
(III) | 24460 | 1-(2-chloroethyl)-2-oxo-1-hydrazinecarbonyl azide | C3H4ClN5O2 | 详情 | 详情 | |
(IV) | 10259 | Ethanol amine;Ethanolamine;2-Aminoethanol; 2-Amino-1-ethanol;2-Aminoethyl alcohol | 141-43-5 | C2H7NO | 详情 | 详情 |