An Improved Synthesis of Amantadine Hydrochloride

被引:15
|
作者
Duong Binh Vu [1 ]
Thinh Van Nguyen [1 ]
Son Trung Le [1 ]
Chau Dinh Phan [2 ]
机构
[1] Vietnam Mil Med Univ, Phuc La Ward, 160 Phung Hung Str, Hanoi, Vietnam
[2] Hanoi Univ Sci & Technol, Sch Chem Engn, Bach Khoa Ward, Bach Khoa Ward, 1 Dai Co Viet Str, Hanoi, Vietnam
关键词
GRIGNARD-REAGENTS; PRIMARY AMINES; ELECTROPHILIC AMINATION; O-SULFONYLOXIME;
D O I
10.1021/acs.oprd.7b00242
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Amantadine hydrochloride 1 is an antiviral drug used in the prevention and treatment of influenza A infections. It has also been used for alleviating early symptoms of Parkinson's disease. Several methods for the preparation of 1 have been reported. These procedures started with adamantane 2 using as many as four reaction steps to produce amantadine hydrochloride with overall yields ranging from 45% to 58%. In this article, we describe a two-step procedure for the synthesis of 1 from 2 via N-(1-adamantyl)acetamide 4 with an improved overall yield of 67%. The procedure was also optimized to reduce the use of toxic solvents and reagents, rendering it more environment-friendly. The procedure can be considered as suitable for largescale production of amantadine hydrochloride. The structure of amantadine hydrochloride was confirmed by H-1 NMR, C-13 NMR, IR, and MS.
引用
收藏
页码:1758 / 1760
页数:3
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