【结 构 式】 |
【分子编号】42495 【品名】4-[[chloro(octadecyloxy)phosphoryl]oxy]-1-methylpiperidinium chloride 【CA登记号】 |
【 分 子 式 】C24H50Cl2NO3P 【 分 子 量 】502.545102 【元素组成】C 57.36% H 10.03% Cl 14.11% N 2.79% O 9.55% P 6.16% |
合成路线1
该中间体在本合成路线中的序号:(IV)Perifosine was synthesized via a two-step process. In the first step, phosphorus oxytrichloride (I) was reacted with 4-hydroxy-1-methylpiperidine hydrochloride (II) in dichloromethane at room temperature using pyridine as auxiliary base. The resulting intermediate, without isolation, was reacted with octadecanol (III) to yield desmethyl perifosine (IV). Desmethyl perifosine was purified by recrystallization prior to methylation. The second step consisted of the methylation of desmethyl perifosine (IV), which was carried out with p-toluenesulfonic acid methyl ester in boiling ethanol using potassium carbonate as base. The crude perifosine solution that was obtained after filtration of the cooled reaction mixture was treated with ion exchange resin in order to remove remaining salts and ionic by-products. Pure perifosine was obtained after evaporation and crystallization.
【1】 Eibl, H.; Engel, J.; Synthesis of hexadecylphosphocholine (miltefosine). Alkylphophocholines: New drugs in cancer therapy. Prog Exp Tumor Res 1992, 34, 1-5. |
【2】 Engel, J.; Hilgard, P.; Nossner, G.; Voss, V.; Traiser, M.; Klenner, T.; Kutscher, B.; Perifosine. Drugs Fut 2000, 25, 12, 1257. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(A) | 23403 | Methyl p-toluenesulfonate; Methyl 4-methylbenzenesulfonate; Methyl 4-toluenesulfonate | 80-48-8 | C8H10O3S | 详情 | 详情 |
(I) | 42493 | Phosphoryl chloride; Phosphorus Oxychloride; Phosphorus (V) trichloride oxide | 10025-87-3 | Cl3OP | 详情 | 详情 |
(II) | 42494 | 4-hydroxy-1-methylpiperidinium chloride | C6H14ClNO | 详情 | 详情 | |
(III) | 21494 | 1-octadecanol | 112-92-5 | C18H38O | 详情 | 详情 |
(IV) | 42495 | 4-[[chloro(octadecyloxy)phosphoryl]oxy]-1-methylpiperidinium chloride | C24H50Cl2NO3P | 详情 | 详情 |