【结 构 式】 |
【分子编号】40947 【品名】[4-(4-nitrobenzoyl)-1-piperazinyl](4-nitrophenyl)methanone 【CA登记号】 |
【 分 子 式 】C18H16N4O6 【 分 子 量 】384.3484 【元素组成】C 56.25% H 4.2% N 14.58% O 24.98% |
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)The acylation of piperazine (II) with 4-nitrobenzoyl chloride (I) afforded a mixture of monoacylated (III) and diacylated (IV) products, which were separated by chromatography. Subsequent alkylation of monosubstituted piperazine (III) with 4-nitrophenethyl bromide (V) in the presence of K2CO3 and NaI yielded the title compound.
【1】 Kanojia, R.M.; Kauffman, J.; Salata, J.J.; Synthesis and class III type antiarrhythmic activity of 4-aroyl (and aryl)-1-aralkylpiperazines. Bioorg Med Chem Lett 2000, 10, 24, 2819. |
【2】 Kanojia, R.M.; et al.; Synthesis and selective class III type antiarrhythmic activity of 4-aroyl (and aryl)-1-aralkylpiperazines. 219th ACS Natl Meet (March 26 2000, San Francisco) 2000, Abst MEDI 204. |
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) | 18941 | p-nitrobenzoyl chloride; 4-nitrobenzoyl chloride | 122-04-3 | C7H4ClNO3 | 详情 | 详情 |
(II) | 10355 | Diethylenediamine; Piperazine | 110-85-0 | C4H10N2 | 详情 | 详情 |
(III) | 20011 | (4-nitrophenyl)(1-piperazinyl)methanone | C11H13N3O3 | 详情 | 详情 | |
(IV) | 40947 | [4-(4-nitrobenzoyl)-1-piperazinyl](4-nitrophenyl)methanone | C18H16N4O6 | 详情 | 详情 | |
(V) | 19191 | 1-(2-bromoethyl)-4-nitrobenzene | 5339-26-4 | C8H8BrNO2 | 详情 | 详情 |
Extended Information