【结 构 式】 |
【分子编号】24788 【品名】1,6-bis(aminooxy)hexane 【CA登记号】 |
【 分 子 式 】C6H16N2O2 【 分 子 量 】148.20532 【元素组成】C 48.63% H 10.88% N 18.9% O 21.59% |
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:(XII)The reaction of benzohydroxamic acid (I) with 1,6-dibromohexane (X) by means of NaOH in methanol gives the bis benzohydroxamic ester (XI), which is treated with HCl to afford the subituted bis hydroxylamine (XII). The reaction of (XII) with dicyandiamide (V) in ethanol yields the bis biguanide (XIII), which is finally cyclized with cyclopentanone (VII) and HCl as before.
【1】 Zhang, X.P.; Shen, J.; Xin, Z.M.; Qiu, Q.P.; Zhou, W.C.; Synthesis and antiprotozoal activities of some new triazine derivatives including a new antitrypanosomal agent: SIPI-1029. Acta Pharm Sin 1996, 31, 11, 823. |
【2】 Zhou, W.; Zhang, X.; Trybizine Hydrochloride. Drugs Fut 1999, 24, 10, 1084. |
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) | 24777 | N-hydroxybenzamide | 495-18-1 | C7H7NO2 | 详情 | 详情 |
(V) | 23611 | N-cyanoguanidine | 461-58-5 | C2H4N4 | 详情 | 详情 |
(VII) | 15113 | cyclopentanone | 120-92-3 | C5H8O | 详情 | 详情 |
(X) | 24786 | 1,6-dibromohexane | 629-03-8 | C6H12Br2 | 详情 | 详情 |
(XI) | 24787 | N-([6-[(benzoylamino)oxy]hexyl]oxy)benzamide | C20H24N2O4 | 详情 | 详情 | |
(XII) | 24788 | 1,6-bis(aminooxy)hexane | C6H16N2O2 | 详情 | 详情 | |
(XIII) | 24789 | 1,6-bis([[[[amino(imino)methyl]amino](imino)methyl]amino]oxy)hexane | C10H24N10O2 | 详情 | 详情 |
Extended Information