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【结 构 式】

【分子编号】31171

【品名】5-amino-1H,3H-benzo[de]isochromene-1,3-dione

【CA登记号】

【 分 子 式 】C12H7NO3

【 分 子 量 】213.19252

【元素组成】C 67.61% H 3.31% N 6.57% O 22.51%

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:(II)

This compound can be obtained by two related ways: 1) The reduction of 3-nitronaphthalene-1,8-dicarboxylic acid anhydride (I) with H2 over Pd/C in DMF gives the corresponding 3-amino-anhydride (II), which is then treated with N,N-dimethylethylenediamine in refluxing toluene or ethanol. (2,3) 2) The reaction of anhydride (I) with N,N-dimethylethylenediamine as before gives 2-[2-(dimethylamino)ethyl]-5-nitro-1H-benz[d,e]isoquinoline-1,3 (2H)-dione (III), which is reduced with H2 or HCOONH4 (4) over Pd/C , or with Sn-HCl at 90-100 C. (1)

1 Brana, M.F.; Martinez Sanz, A.; Perez Alvarez-Ossorio, R.; Martinez Roldan, C.; Rodan Fernandez de Gamboa, C. (Made Labs.); Naphthalimides, process for their preparation and pharmaceutical compositions containing them. DE 2823987 .
2 Nishimura, N.; Askew, B.; Patel, V.F.; Elbaum, D.; Habgood, G.; Kim, J.L.; Handley, M.; Booker, S.; Germain, J.; Kim, T.-S.; Yuan, C.C. (Amgen Inc.); Substd. benzylamine derivs. and methods of use. US 2003134836; WO 0407457 .
3 Castaner, J.; Castaner, R.M.; Eastland, G.; Amonafide. Drugs Fut 1990, 15, 9, 879.
4 Zee-Cheng, R.K.Y.; Cheng, C.C.; N-(Aminoalkyl)imide antineoplastic agents. Synthesis and biological activity. J Med Chem 1985, 28, 9, 1216-22.
5 Fernández Braña, M.; Martínez Sanz, A.; Castellano, J.M.; Martínez Roldan, C.; Roldan Fernández de Gamboa, C.; Synthesis and cytostatic activity of benz(de)isoquinolin-1,3-diones. Structure-activity relationships. Eur J Med Chem - Chim Ther 1981, 16, 3, 207-212.
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) 15864 5-nitro-1H,3H-benzo[de]isochromene-1,3-dione; 3-Nitro-1,8-naphthalic anhydride 3027-38-1 C12H5NO5 详情 详情
(II) 31171 5-amino-1H,3H-benzo[de]isochromene-1,3-dione C12H7NO3 详情 详情
(III) 31172 2-[2-(dimethylamino)ethyl]-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione C16H15N3O4 详情 详情
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