合成路线:Naratriptan can be obtained by several related ways:1) The reaction of 5-bromoindole (I) with 1-methylpiperidin-4-one (II) by means of KOH in methylated spirit (or methanol) at room temperature gives 5-bromo-3-(4-(hydroxy-1-methylpiperidin-4-yl)-1H-indole (III) (1,2),which is condensed with N-methylvinylsulfonamide (IV) by means of palladium acetate and tri-p-tolyl phosphine in hot (110 C) DMF to afford (E)-N-methyl-2-[3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl]vinylsulfonamide (V).Finally,this compound is hydrogenated with H2 over Pd/C in DMF/water/HCl,DMF/water/methanol/HCl,or water/methanesulfonic acid.2) The reaction of indole (I) with piperidone (II) or with 4-hydroxy-1-methylpiperidine (VI) by means of KOH in refluxing methylated spirit or 1-propanol gives 5-bromo-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (VII),which is then condensed with N-methylvinylsufonamide (IV) as before,yielding the substituted sulfonamide (V),already obtained.3) The hydrogenation of the tetrahydropyridine (VII) with H2 over PtO2 in methanol/HCl gives 5-bromo-3-(1-methylpiperidin-4-yl)-1H-indole (VIII),which is finally condensed with N-methylvinylsulfonamide (IV) as before yielding N-methyl-2-[3-(1-methylpiperidin-4-yl)-1H-indol-5-yl]vinylsulfonamide (XI).Finally,this compound is hydrogenated with H2 over Pd/C in ethanol/DMF/HCl.4) The reaction of 5-bromoindole (I) with sulfonamide (IV) by means of palladium acetate as before gives 2-(1H-indol-3-yl)-N-methylvinylsulfonamide (IX),which is condensed with piperidone (II) by means of refluxing KOH as before,yielding the substituted tetrahydropyridine (V),already obtained.5) The condensation of sulfonamide (IX) with piperidone (II),by means of KOH at room temperature as before gives N-methyl-2-[3-(4-hydroxy-1-methylpiperidin-4-yl)-1H-indol-3-yl] vinylsulfonamide (X),which is dehydrated to tetrahydropyridine (V) with KOH in refluxing methylated spirit.6) The cyclization of 2-(4-hydrazinophenyl)-N-methylethanesulfonamide (XII) with 2-(1-methylpiperidin-4-yl)acetaldehyde (XIII) by means of HCl in water.7) The reaction of 2-(1H-indol-5-yl)-N-methylethanesulfonamide (XIV) with piperidone (II) by means of KOH in refluxing methanol,yielding N-methyl-2-[3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl] ethylsulfonamide (XV),which is finally hydrogenated with H2 over Pd/C in ethanol/DMF.
参考文献标题:Process for the preparation of N-methyl-3-(1-methyl-4-piperidinyl)-1H-indole-5-ethanesulfonamide
文献作者:Blatcher,P.; Carter,M.; Hornby,R.; Owen,M.R.(Glaxo Wellcome plc)
参考来源:WO 9509166
合成路线:Naratriptan can be obtained by several related ways:1) The reaction of 5-bromoindole (I) with 1-methylpiperidin-4-one (II) by means of KOH in methylated spirit (or methanol) at room temperature gives 5-bromo-3-(4-(hydroxy-1-methylpiperidin-4-yl)-1H-indole (III) (1,2),which is condensed with N-methylvinylsulfonamide (IV) by means of palladium acetate and tri-p-tolyl phosphine in hot (110 C) DMF to afford (E)-N-methyl-2-[3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl]vinylsulfonamide (V).Finally,this compound is hydrogenated with H2 over Pd/C in DMF/water/HCl,DMF/water/methanol/HCl,or water/methanesulfonic acid.2) The reaction of indole (I) with piperidone (II) or with 4-hydroxy-1-methylpiperidine (VI) by means of KOH in refluxing methylated spirit or 1-propanol gives 5-bromo-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (VII),which is then condensed with N-methylvinylsufonamide (IV) as before,yielding the substituted sulfonamide (V),already obtained.3) The hydrogenation of the tetrahydropyridine (VII) with H2 over PtO2 in methanol/HCl gives 5-bromo-3-(1-methylpiperidin-4-yl)-1H-indole (VIII),which is finally condensed with N-methylvinylsulfonamide (IV) as before yielding N-methyl-2-[3-(1-methylpiperidin-4-yl)-1H-indol-5-yl]vinylsulfonamide (XI).Finally,this compound is hydrogenated with H2 over Pd/C in ethanol/DMF/HCl.4) The reaction of 5-bromoindole (I) with sulfonamide (IV) by means of palladium acetate as before gives 2-(1H-indol-3-yl)-N-methylvinylsulfonamide (IX),which is condensed with piperidone (II) by means of refluxing KOH as before,yielding the substituted tetrahydropyridine (V),already obtained.5) The condensation of sulfonamide (IX) with piperidone (II),by means of KOH at room temperature as before gives N-methyl-2-[3-(4-hydroxy-1-methylpiperidin-4-yl)-1H-indol-3-yl] vinylsulfonamide (X),which is dehydrated to tetrahydropyridine (V) with KOH in refluxing methylated spirit.6) The cyclization of 2-(4-hydrazinophenyl)-N-methylethanesulfonamide (XII) with 2-(1-methylpiperidin-4-yl)acetaldehyde (XIII) by means of HCl in water.7) The reaction of 2-(1H-indol-5-yl)-N-methylethanesulfonamide (XIV) with piperidone (II) by means of KOH in refluxing methanol,yielding N-methyl-2-[3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl] ethylsulfonamide (XV),which is finally hydrogenated with H2 over Pd/C in ethanol/DMF.
参考文献标题:Naratriptan
文献作者:Mealy,N.; Castar,J.
参考来源:Drugs Fut 1996,21(5),476
产品链接: CAS No. 143388-64-1›› 产品链接: CAS No.121679-13-8››