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项目整合精选>>>Mometasone furoate, S-2640, Sch-32088, Asmanex Twisthaler, Asmanex, Nasonex, Altosone, Fulmeta, Ecotone, Ecural, Elocon
Mometasone furoate, S-2640, Sch-32088, Asmanex Twisthaler, Asmanex, Nasonex, Altosone, Fulmeta, Ecotone, Ecural, Elocon
糠酸莫米松Chemical Name: 9,21-Dichloro-11beta,17-dihydroxy-16alpha-methylpregna-1,4-diene-3,20-dione 17-furoate
CAS No. 83919-23-7
项目整合开发状态: Launched-1987
项目研究机构: Essex (Originator), Schering-Plough (Originator), Shionogi (Licensee)
合成路线:The reaction of 9beta,11beta-epoxy-17alpha,21-dihydroxy-16alpha-methyl-1,4-pregnadiene-3,20-dione (I) with MsCl in pyridine gives the corresponding 21-mesylate (II),which is treated with LiCl in the same solvent to yield 21-chloro-9beta,11beta-epoxy-17alpha-hydroxy-16alpha-methyl-1,4-pregnadiene-3,20-dione (III).The esterification of (III) with 2-furoyl chloride (IV) and TEA affords the expected ester (IV),which is finally treated with anhydrous HCl in acetic acid in order to open the epoxide ring to provide the target mometasone furoate.A similar reaction sequence can be performed using p-toluenesulfonyl chloride instead of mesyl chloride in the first step of the sequence.
合成路线:The esterification of 21-chloro-17alpha-hydroxy-16alpha-methyl-1,4,9(11)-pregnatriene-3,20-dione (I) with 2-furoyl chloride (II) by means of TEA gives the corresponding ester (III),which is then treated with HClO4 and 1,3-dichloro-5,5-dimethylhydantoin (DDH) in THF/water in order to add Cl-OH to the 9(11)-double bond of ester (III).
📌 参考资料/链接:
参考文献标题:3,20-Dioxo-1,4-pregnanediene-17alpha-ol 17-aromatic heterocycle carboxylates
文献作者:Shapiro,E.L.(Schering Corp.)
参考来源:EP 0057401; US 4472393
📄 详细内容
合成路线:By esterification of mometasone (I) with 2-furoyl chloride (II) by means of TEA in dichloromethane.
参考文献标题:Process for the preparation of mometasone furoate
文献作者:Heggie,W.; Bandarra,J.(Hovione Sociedade Quimica SA)
参考来源:EP 1074558; JP 2001048897
合成路线:The reaction of 9beta,11beta-epoxy-17alpha,21-dihydroxy-16alpha-methyl-1,4-pregnadiene-3,20-dione (I) with MsCl in pyridine gives the corresponding 21-mesylate (II),which is treated with LiCl in the same solvent to yield 21-chloro-9beta,11beta-epoxy-17alpha-hydroxy-16alpha-methyl-1,4-pregnadiene-3,20-dione (III).The esterification of (III) with 2-furoyl chloride (IV) and TEA affords the expected ester (IV),which is finally treated with anhydrous HCl in acetic acid in order to open the epoxide ring to provide the target mometasone furoate.A similar reaction sequence can be performed using p-toluenesulfonyl chloride instead of mesyl chloride in the first step of the sequence.
参考文献标题:Process for the preparation of 17-esters of 9alpha,21-dihalo-pregnane-11beta,17alpha-diol-20-ones
文献作者:Tann,C.-H.; Tsai,D.J.S.; Kwok,D.-I.; Fu,X.(Schering Corp.)
参考来源:WO 9800437
产品链接: CAS No. 83919-23-7››