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【结 构 式】

【分子编号】24141

【品名】N-(10,11-dithia-7,14,21-triazadocos-1-yl)-N-methylamine

【CA登记号】

【 分 子 式 】C18H42N4S2

【 分 子 量 】378.69044

【元素组成】C 57.09% H 11.18% N 14.79% S 16.94%

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)

N1,N1'-Dithiobis(ethane-2,1-diyl)bis(hexane-1,6-diamine) (II) is prepared starting from 6-aminohexylcyste amine (I) by potassium ferricyanide oxidation. The condensation of (II) with pyrrol 2-carboxaldehyde and subsequent reduction with NaHB4 of the resulting Schitf base gives (III), which is crvstallized as tetraoxatate.

1 Angeli, P.; et al.; Structure-activity relationships among benextramine-related tetraamine disulfides at peripheral alpha-adrenoreceptors. J Med Chem 1985, 28, 11, 1643.
2 Brasili, L.; Pyrextramine. Drugs Fut 1986, 11, 1, 32.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
21081 Pyrrole-2-carbaldehyde; 1H-pyrrole-2-carbaldehyde 1003-29-8 C5H5NO 详情 详情
(I) 24140 2-[[6-(methylamino)hexyl]amino]-1-ethanethiol C9H22N2S 详情 详情
(II) 24141 N-(10,11-dithia-7,14,21-triazadocos-1-yl)-N-methylamine C18H42N4S2 详情 详情
Extended Information