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目的研究二甲磺酸赖右苯丙胺的合成工艺。方法以1-苯基-2-丙酮、S-苯乙胺为原料,在三乙酰氧基硼氢化钠作用下进行不对称还原胺化得到(S)-1-苯基-N-((S)-1-苯乙基)丙烷-2-胺(2),2在Pd/C作用下脱苄基得到(1S)-1-甲基-2-苯乙基胺(3);以L-赖氨酸盐酸盐为原料,经二碳酸二叔丁酯保护得到(S)-2,6-双((叔丁氧基羰基)氨基)己酸(4);中间体3和4在1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐和1-羟基苯并三唑作用下经缩合反应得到(2S)-2,6-二-N-Boc-氨基-N-[(1S)-1-甲基-2-苯乙基]己酸胺(5),5在甲磺酸中脱Boc保护基并成盐制得目标物(2S)-2,6-二氨基-N-[(1S)-1-甲基-2-苯乙基]己酸胺二甲磺酸盐。结果与结论目标产物的结构经1H-NM R、13C-NM R、DEPT和HRM S谱确证,总收率为50.5%(以S-苯乙胺计)。本文采用的合成路线具有原料成本低、操作简单高效、立体选择性好、收率高等优点,更适宜工业化生产。
Objective To study the synthesis of levamisole dimethanesulfonate. Methods Asymmetric reductive amination of 1-phenyl-2-propanone and S-phenylethylamine in the presence of sodium triacetoxyborohydride gave (S) -1-phenyl- (2), 2 was debenzylated with Pd / C to give (1S) -1-methyl-2-phenylethylamine (3) (S) -2,6-bis ((tert-butoxycarbonyl) amino) hexanoic acid (4) was obtained by using lysine hydrochloride as a starting material and di (tert- (2S) -2,6-di-N-Boc-N-methyloctanoic acid under the action of ethyl- (3-dimethylaminopropyl) carbodiimide hydrochloride and 1-hydroxybenzotriazole. (5), 5) deprotection of Boc in methanesulfonic acid and salt formation to obtain the target (2S) -2, 6-Diamino-N - [(1S) -1-methyl-2-phenylethyl] hexanoic acid amine dimethanesulfonate. Results and Conclusions The structure of the target product was confirmed by 1H-NM R, 13C-NM R, DEPT and HRM S spectra. The overall yield was 50.5% (as S-phenylethylamine). The synthesis route used in this paper has the advantages of low cost of raw materials, simple and efficient operation, good stereoselectivity and high yield, and is more suitable for industrialized production.