【结 构 式】 |
【分子编号】50898 【品名】Octahydro-1H-1,4,7-triazonine; 1,4,7-Triazacyclononane; Triethylenetriamine 【CA登记号】4730-54-5 |
【 分 子 式 】C6H15N3 【 分 子 量 】129.20532 【元素组成】C 55.78% H 11.7% N 32.52% |
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:(I)Condensation of 1,4,7-triazacyclononane (I) with 4,7-dichloroquinoline (II) produced the disubstituted derivative (III). Then, coupling of glutaric acid (IV) with amine (III) using bromo-tris-pyrrolidinophosphonium hexafluorophosphate gave the corresponding diamide.
【1】 Girault, S.; Grellier, P.; Sergheraert, C.; Lemière, P.; Maes, L.; Davioud-Charvet, E.; Berceibar, A.; Mouray, E.; Antiplasmodial activity and cytotoxicity of bis-, tris-, and tetraquinolines with linear or cyclic amino linkers. J Med Chem 2001, 44, 11, 1658. |
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) | 50898 | Octahydro-1H-1,4,7-triazonine; 1,4,7-Triazacyclononane; Triethylenetriamine | 4730-54-5 | C6H15N3 | 详情 | 详情 |
(II) | 38277 | 4,7-dichloroquinoline | 86-98-6 | C9H5Cl2N | 详情 | 详情 |
(III) | 50899 | 7-chloro-4-[4-(7-chloro-4-quinolinyl)-1,4,7-triazonan-1-yl]quinoline | C24H23Cl2N5 | 详情 | 详情 | |
(IV) | 50900 | Pentanedioic Acid; 1,5-Pentanedioic acid; 1,3-Propanedicarboxylic acid; Glutaric acid | 110-94-1 | C5H8O4 | 详情 | 详情 |
Extended Information