网站主页>>>项目整合精选>>>项目整合精选>>>Eszopiclone, (+)-Zopiclone, (S)-Zopiclone, Estorra

Eszopiclone, (+)-Zopiclone, (S)-Zopiclone, Estorra

右佐匹克隆 (R)-佐匹克隆 Chemical Name: (+)-6-(5-Chloro-2-pyridyl)-7(S)-(4-methylpiperazin-1-ylcarbonyloxy)-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-one; (+)-4-Methylpiperazine-1-carboxylic acid 6-(5-chloro-2-pyridyl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5(S)-yl ester
CAS No. 138729-47-2, 138680-08-7 ((R)-isomer)
项目整合开发状态: Pre-Registered
项目研究机构: Aventis Pharma (Originator), Sepracor (Licensee)
合成路线:The esterification of (rac)-6-(5-chloro-3-pyridyl)-5-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-7-one rac-(I) with vinyl chloroformate (II) in pyridine gives the racemic carbonate rac-(III),which is submitted to an enantioselective hydrolysis with Candida antarctica (SP 435L) lipase in dioxane/benzyl alcohol yielding a mixture of rac-(I),which is recycled,and enantiomerically pure (95% e.e.) (S)-(III).Finally,this compound is condensed with 1-methylpiperazine (IV) in acetone.

合成路线:Eszopiclone can also be obtained by optical resolution of zopiclone by several different methods:i) crystallization of the D-(+)-O,O'-dibenzoyltartaric acid salt in acetonitrile,followed by treatment with NaOH in dichloromethane/water; ii) crystallization of the (+)-malic acid salt in MeOH/acetone followed by treatment with KHCO3 in MeOH water and extraction with dichloromethane/ethyl acetate;iii) chiral chromatography over a Chiralpak AS column; iv) capillary electrophoresis in the presence of octakis-(2,3,6-tri-O-methyl)-g-cyclodextrin.
📌 参考资料/链接:
参考文献标题:Optically active deriv.of 5H-pyrrolo[3,4-b]pyrazine,its preparation and pharmaceutical compsns.containing it
文献作者:Cotrel,C.; Roussel,G.(Aventis Pharma SA)
参考来源:EP 0495717; EP 0609210; FR 2671800; JP 1994504548; WO 9212980

📄 详细内容


合成路线:The esterification of (rac)-6-(5-chloro-3-pyridyl)-5-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-7-one rac-(I) with vinyl chloroformate (II) in pyridine gives the racemic carbonate rac-(III),which is submitted to an enantioselective hydrolysis with Candida antarctica (SP 435L) lipase in dioxane/benzyl alcohol yielding a mixture of rac-(I),which is recycled,and enantiomerically pure (95% e.e.) (S)-(III).Finally,this compound is condensed with 1-methylpiperazine (IV) in acetone.

参考文献标题:(+)-6-(5-Chloropyrid-2-yl)-7-oxo-vinylcarbonyloxy-5,6-dihydropyrrolo[3,4b]pyrazine and their use in a process for the preparation of (+)-6-(5-chloropyrid-2-yl)-5-(4-methylpiperazin-1-yl)-carbonyloxy-7-oxo-5,6-dihydropyrrolo[3,4b]pyrazine
文献作者:Bayod Jasanada,M.S.; Brieva Collado,R.; Linares L髉ez,F.J.; Garc韆 Campos,R.; Gotor Santamar韆,V.(Asturpharma SA)
参考来源:ES 2101653


合成路线:The reaction of pyrazine-2,3-dicarboxylic acid anhydride (I) with 2-amino-5-chloropyridine (II) in refluxing acetonitrile gives 3-(5-chloro-2-pyridyl)carbamoyl pyrazine-2-carboxylic acid (III),which is cyclized by treatment with refluxing SOCl2 affording 6-(5-chloropyrid-2-yl)-5,7-dioxo-5,6-dihydropyrrolo[3,4-b]pyrazine (IV).The partial reduction of (IV) with KBH4 in dioxane-water yields 6-(5-chloro-2-pyridyl)-7-hydroxy-5,6-dihydropyrrolo[3,4-b]pyrazin-5-one (V),which is finally esterified with 4-methylpiperazine-1-carbonyl chloride (VI) by means of NaH in DMF.

合成路线:The esterification of (rac)-6-(5-chloro-3-pyridyl)-5-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-7-one rac-(I) with vinyl chloroformate (II) in pyridine gives the racemic carbonate rac-(III),which is submitted to an enantioselective hydrolysis with Candida antarctica (SP 435L) lipase in dioxane/benzyl alcohol yielding a mixture of rac-(I),which is recycled,and enantiomerically pure (95% e.e.) (S)-(III).Finally,this compound is condensed with 1-methylpiperazine (IV) in acetone.

合成路线:The esterification of (rac)-6-(5-chloro-3-pyridyl)-5-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-7-one rac-(I) with chloromethyl chloroformate (V) in pyridine gives the racemic carbonate rac-(III),which is submitted to an enantioselective hydrolysis with Candida antarctica (SP 435L) lipase in dioxane/benzyl alcohol yielding a mixture of rac-(I),which is recycled,and enantiomerically pure (96% e.e.) (S)-(III).Finally,this compound is condensed with 1-methylpiperazine (IV) in acetone.

参考文献标题:Pyrrolo-[3,4,b]pyrazine derivatives
文献作者:Cotrel,C.; et al.(Aventis Pharma SA)
参考来源:DE 2300491; GB 1358680; JP 52048687; US 3862149


合成路线:The esterification of (rac)-6-(5-chloro-3-pyridyl)-5-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-7-one rac-(I) with vinyl chloroformate (II) in pyridine gives the racemic carbonate rac-(III),which is submitted to an enantioselective hydrolysis with Candida antarctica (SP 435L) lipase in dioxane/benzyl alcohol yielding a mixture of rac-(I),which is recycled,and enantiomerically pure (95% e.e.) (S)-(III).Finally,this compound is condensed with 1-methylpiperazine (IV) in acetone.

合成路线:The esterification of (rac)-6-(5-chloro-3-pyridyl)-5-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-7-one rac-(I) with chloromethyl chloroformate (V) in pyridine gives the racemic carbonate rac-(III),which is submitted to an enantioselective hydrolysis with Candida antarctica (SP 435L) lipase in dioxane/benzyl alcohol yielding a mixture of rac-(I),which is recycled,and enantiomerically pure (96% e.e.) (S)-(III).Finally,this compound is condensed with 1-methylpiperazine (IV) in acetone.

参考文献标题:Enzymic resolution of (?-6-(5-chloropyridin-2-yl)-7-vinyloxycarbonyloxy-6,7-dihydro[5H] pyrrolo[3,4-b]pyrazin-5-one.Synthesis of (+)-zopiclone
文献作者:Gotor,V.; et al.
参考来源:Tetrahedron Asymmetry 1997,8(7),995


合成路线:Eszopiclone can also be obtained by optical resolution of zopiclone by several different methods:i) crystallization of the D-(+)-O,O'-dibenzoyltartaric acid salt in acetonitrile,followed by treatment with NaOH in dichloromethane/water; ii) crystallization of the (+)-malic acid salt in MeOH/acetone followed by treatment with KHCO3 in MeOH water and extraction with dichloromethane/ethyl acetate;iii) chiral chromatography over a Chiralpak AS column; iv) capillary electrophoresis in the presence of octakis-(2,3,6-tri-O-methyl)-g-cyclodextrin.

合成路线:The title compound has been obtained from racemic zopliclone (I) by several related procedures.Demethylation of (I) to afford (II) has been achieved by treatment with diethyl azodicarboxylate (DEAD) in boiling toluene,followed by mild hydrolysis with NH4Cl in refluxing EtOH.In a higher yield demethylation procedure,treatment of (I) with chloroethyl chloroformate produced carbamate (III),which was further hydrolyzed to (II) in boiling MeOH.Resolution of racemic N-demethyl zopiclone (II) has been accomplished via formation of the diastereomeric salts with N-Z-L-phenylalanine or,alternatively,by means of semi-preparative chiral HPLC.In a related strategy,racemic zopiclone (I) was first resolved using D-malic acid to provide the (S)-enantiomer (IV).This was then dealkylated by means of either DEAD or employing the chloroethyl chloroformate method.

参考文献标题:Semi-preparative chiral resolution of zoplicone and N-desmethylzopiclone
文献作者:Mannaert,E.; Daenens,P.
参考来源:J Pharm Biomed Anal 1996,14(8-10),1367


合成路线:The esterification of (rac)-6-(5-chloro-3-pyridyl)-5-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-7-one rac-(I) with chloromethyl chloroformate (V) in pyridine gives the racemic carbonate rac-(III),which is submitted to an enantioselective hydrolysis with Candida antarctica (SP 435L) lipase in dioxane/benzyl alcohol yielding a mixture of rac-(I),which is recycled,and enantiomerically pure (96% e.e.) (S)-(III).Finally,this compound is condensed with 1-methylpiperazine (IV) in acetone.

参考文献标题:Enzymatic resolution of new carbonate intermediates for the synthesis of (S)-(+)-zopiclone
文献作者:Solares,L.F.; D韆z,M.; Brieva,R.; S醤chez,V.M.; Bayod,M.; Gotor,V.
参考来源:Tetrahedron Asymmetry 2002,13(23),2577


合成路线:Eszopiclone can also be obtained by optical resolution of zopiclone by several different methods:i) crystallization of the D-(+)-O,O'-dibenzoyltartaric acid salt in acetonitrile,followed by treatment with NaOH in dichloromethane/water; ii) crystallization of the (+)-malic acid salt in MeOH/acetone followed by treatment with KHCO3 in MeOH water and extraction with dichloromethane/ethyl acetate;iii) chiral chromatography over a Chiralpak AS column; iv) capillary electrophoresis in the presence of octakis-(2,3,6-tri-O-methyl)-g-cyclodextrin.

参考文献标题:Separation of enantiomers of drugs by capillary electrophoresis with permethyl-gamma-cyclodextrin as chiral solvating agent
文献作者:Koppenhoefer,B.; Jakob,A.; Zhu,X.; Lin,B.
参考来源:HRC - J High Resolut Chromatogr 2000,23(6),413


产品链接: CAS No. 138729-47-2››

产品链接: CAS No.138680-08-7››