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【结 构 式】 
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【分子编号】23914 【品名】4-methyl-3-nitrobenzoyl chloride 【CA登记号】10397-30-5 |
【 分 子 式 】C8H6ClNO3 【 分 子 量 】199.59328 【元素组成】C 48.14% H 3.03% Cl 17.76% N 7.02% O 24.05% |
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)Several procedures for obtaining titte compound have been reported: In one method the acylation of 1 naphthylamine 4,6,8-trisulfonic acid trisodium salt (I) with 4 methyl-3-nitrobenzoyt chloride (II) yields the correspond ing amide (III), which is reduced with Fe in acetic acid to the amine (IV). Acylation of (IV) with 3-nitrobenzoyl chloride (V) affords the nitro diamide (VI), which is reduced with Fe and acetic acid before to the amine (VII). Finally, this compound is condensed with phosgene.
| 【1】 Heymann; Angew Chem 1924, 37, 585. |
| 【2】 Freres, P.; Foruneau, E.; Trefouel, J.; The manufacture of a symmetrical urea of m-aminobenzoyl-m-aminomethylbenzoyl-1-napthylamino-4,6,8-trisulphonate of sodium. GB 224849 . |
| 【3】 Fourneau; et al.; Compt Rend Acad Sci 1924, 178, 675. |
| 【4】 Castaner, J.; Serradell, M.N.; Suramin Sodium. Drugs Fut 1986, 11, 10, 860. |
| 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) | 23913 | 8-Aminonaphthalene-1,3,5-trisulfonic acid trisodium salt | C10H6NNa3O9S3 | 详情 | 详情 | |
| (II) | 23914 | 4-methyl-3-nitrobenzoyl chloride | 10397-30-5 | C8H6ClNO3 | 详情 | 详情 |
| (III) | 23915 | 4-Methyl-3-nitro-N-(4,6,8-trisulfonaphthalen-1-yl)benzamide trisodium salt | C18H11N2Na3O12S3 | 详情 | 详情 | |
| (IV) | 23916 | 3-Amino-4-methyl-N-(4,6,8-trisulfonaphthalen-1-yl)benzamide trisodium salt | C18H13N2Na3O10S3 | 详情 | 详情 | |
| (V) | 15293 | 3-nitrobenzoyl chloride; m-nitrobenzoyl chloride | 121-90-4 | C7H4ClNO3 | 详情 | 详情 |
| (VI) | 23918 | 4-Methyl-3-(3-nitrobenzamido)-N-(4,6,8-trisulfonaphthalen-1-yl)benzamide trisodium salt | C25H16N3Na3O13S3 | 详情 | 详情 | |
| (VII) | 23919 | 3-(3-Aminobenzamido)-4-methyl-N-(4,6,8-trisulfonaphthalen-1-yl)benzamide trisodium salt | C25H18N3Na3O11S3 | 详情 | 详情 |
Extended Information