Trapped in Misbelief for Almost 40 Years: Selective Synthesis of the Four Stereoisomers of Mefloquine

被引:13
作者
Schuetzenmeister, Nina [1 ]
Mueller, Michael [1 ]
Reinscheid, Uwe M. [1 ]
Griesinger, Christian [1 ]
Leonov, Andrei [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept NMR Based Struct Biol, D-37077 Gottingen, Germany
关键词
domino reactions; drug design; mefloquine; structure elucidation; total synthesis; ABSOLUTE-CONFIGURATION; ANTIMALARIAL ACTIVITY; ASYMMETRIC-SYNTHESIS; HYDROCHLORIDE; INHIBITION; ENANTIOMER; ALKALOIDS; ALCOHOLS; EFFICACY;
D O I
10.1002/chem.201303403
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here we report the synthesis of all four stereoisomers of mefloquine. Mefloquine (Lariam) is an important anti-malaria drug that is applied as a racemate of the erythro form. However, the (-)-isomer induces psychosis, while the (+)-enantiomer does not have this undesired side effect. There are six syntheses of which five lead to the wrong enantiomer without the authors of these syntheses noting that they had synthesized the wrong compound. At the same time physical chemistry investigations had assigned the absolute configuration correctly and the last enantioselective synthesis that took these results into account delivered the correct absolute configuration. Since various synthetic approaches failed to provide the correct stereoisomers in previous syntheses, we submit here a synthetic approach with a domino Sonogashira-6-electrocyclisation as key step that confirmed synthetically the correct absolute configuration of all four isomers.
引用
收藏
页码:17584 / 17588
页数:5
相关论文
共 45 条
[1]   A new general access to either type of Securinega alkaloids:: Synthesis of securinine and (-)-allonorsecurinine [J].
Alibés, R ;
Ballbé, M ;
Busqué, F ;
de March, P ;
Elias, L ;
Figueredo, M ;
Font, J .
ORGANIC LETTERS, 2004, 6 (11) :1813-1816
[2]  
[Anonymous], ANGEW CHEM
[3]  
[Anonymous], ANGEW CHEM
[4]   Identification of (+)-Erythro-Mefloquine as an Active Enantiomer with Greater Efficacy than Mefloquine against Mycobacterium avium Infection in Mice [J].
Bermudez, Luiz E. ;
Inderlied, Clark B. ;
Kolonoski, Peter ;
Chee, Christopher B. ;
Aralar, Priscilla ;
Petrofsky, Mary ;
Parman, Toufan ;
Green, Carol E. ;
Lewin, Anita H. ;
Ellis, William Y. ;
Young, Lowell S. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (08) :4202-4206
[5]   Stereoselective three-carbon and two-carbon elongation of the carbon chain in N-boc-protected α-aminoacylsilanes:: An entry to functionalized β-amino alcohols and to statine analogues [J].
Bonini, BF ;
Comes-Franchini, M ;
Fochi, M ;
Laboroi, F ;
Mazzanti, G ;
Ricci, A ;
Varchi, G .
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (21) :8008-8013
[6]   OPTICAL ISOMERS OF ARYL-2-PIPERIDYLMETHANOL ANTIMALARIAL AGENTS - PREPARATION, OPTICAL PURITY, AND ABSOLUTE STEREOCHEMISTRY [J].
CARROLL, FI ;
BLACKWELL, JT .
JOURNAL OF MEDICINAL CHEMISTRY, 1974, 17 (02) :210-219
[7]   Absolute Configuration and Antimalarial Activity of erythro-Mefloquine Enantiomers [J].
Dassonville-Klimpt, Alexandra ;
Cezard, Christine ;
Mullie, Catherine ;
Agnamey, Patrice ;
Jonet, Alexia ;
Da Nascimento, Sophie ;
Marchivie, Mathieu ;
Guillon, Jean ;
Sonnet, Pascal .
CHEMPLUSCHEM, 2013, 78 (07) :642-646
[8]  
Devant R. M., 1996, STEREOSELECTIVE SYNT, V2, P1151
[9]   Concise Synthesis and Antimalarial Activity of All Four Mefloquine Stereoisomers Using a Highly Enantioselective Catalytic Borylative Alkene Isomerization [J].
Ding, Jinyue ;
Hall, Dennis G. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (31) :8069-8073
[10]   Artemisinin combination therapy for vivax malaria [J].
Douglas, Nicholas M. ;
Anstey, Nicholas M. ;
Angus, Brian J. ;
Nosten, Francois ;
Price, Ric N. .
LANCET INFECTIOUS DISEASES, 2010, 10 (06) :405-416