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【结 构 式】

【分子编号】24460

【品名】1-(2-chloroethyl)-2-oxo-1-hydrazinecarbonyl azide

【CA登记号】

【 分 子 式 】C3H4ClN5O2

【 分 子 量 】177.54996

【元素组成】C 20.29% H 2.27% Cl 19.97% N 39.44% O 18.02%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(III)

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

合成路线2

该中间体在本合成路线中的序号:(IV)

2) By condensation of (I) with N-(2-chloroethyl)-N-nitrosocarbamoyl hydrazide (IV) in ethanol with triethylamine as catalyst.

1 Carlsson, J.-I.; Jensen, P.H.G.; Stamvik, A.R. (Leo Pharma AB); N-nitroso compounds and compositions containing such compounds. EP 0106123; JP 59073562; US 4613695 .
2 Prous, J.; Castaner, J.; Tauromustine. Drugs Fut 1986, 11, 7, 585.
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) 24457 3-amino-N,N-dimethyl-1-propanesulfonamide C5H14N2O2S 详情 详情
(IV) 24460 1-(2-chloroethyl)-2-oxo-1-hydrazinecarbonyl azide C3H4ClN5O2 详情 详情
Extended Information