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【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