氘代丁苯那嗪合成工艺优化  被引量:2

Improved Synthesis of Deutetrabenazine

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作  者:李国靖 马潇[1,2] 贾萌 李建其 刘育[1,2] LI Guojing;MA Xiao;JIA Meng;LI Jianqi;LIU Yu(Novel Technology Center of Pharmaceutical Chemistry,Shanghai Institute of Pharmaceutical Industry,China State Institute of Pharmaceutical Industry,Shanghai 201203;Shanghai Engineering Research Center of Pharmaceutical Process,Shanghai 201203)

机构地区:[1]中国医药工业研究总院上海医药工业研究院,化学制药新技术中心,上海201203 [2]上海药物合成工艺过程工程技术研究中心,上海201203

出  处:《中国医药工业杂志》2021年第12期1595-1598,共4页Chinese Journal of Pharmaceuticals

摘  要:盐酸多巴胺、三乙胺和甲酸乙酯反应得N-[2-(3,4-二羟基苯基)乙基]甲酰胺(9)。9和三氯氧磷在乙酸乙酯中脱水形成6,7-二羟基-3,4-二氢异喹啉(11)。11和三苯基膦、氘代甲醇、偶氮二甲酸二异丙酯在四氢呋喃中反应得6,7-二(甲氧基-d_(3))-3,4-二氢异喹啉(6),此步骤通过采用氯化锌和调节后处理时反应体系的pH值可革除柱色谱纯化。6和(2-乙酰基-4-甲基戊基)三甲基碘化铵(7)在碳酸钾作用下反应得氘代丁苯那嗪(1)粗品,再经甲醇重结晶即可得纯品,总收率约49%,纯度99.6%。优化后的工艺简便,无需柱色谱纯化。Dopamine hydrochloride(8) reacted with triethylamine and ethyl formate to get N-[2-(3,4-dihydroxyphenyl)ethyl]formamide(9).The dehydration reaction occurred between compound 9 and phosphorus oxychloride in ethyl acetate to obtain 6,7-dihydroxy-3,4-dihydroisoquinoline(11).Compound 11 reacted with triphenylphosphine,deuterated methanol and diisopropyl azodicarboxylate in tetrahydrofuran to obtain 6,7-bis(methoxy-d_(3))-3,4-dihydroisoquinoline(6),in which column chromatography can be eliminated by using zinc chloride and adjusting pH value of the reaction solution in the work-up.Compound 6 reacted with (2-acetyl-4-methylpentyl)trimethyl-1-aminium iodide(7) in the presence of potassium carbonate to obtain crude deuterated tetrabenazine(1).After recrystallization from methanol,the purity of deutetrabenazine reached to 99.6%.In this route,experimental operations were simplified and the column chromatography was avoided.

关 键 词:氘代丁苯那嗪 亨廷顿病 迟发性运动障碍 抽动秽语综合征 合成 

分 类 号:R971[医药卫生—药品]

 

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