反应详情

Potassium hydroxide (0.773 g) was added to a cold solution of methyl 2-amino-5-[1-(1-methyl-4-piperidyl)pyrazol-4-yl]pyridine-3-carboxylate (2.172 g) in methanol (50 ml) and water (5 ml). The resulting mixture was stirred at room temperature during 48 hours. A 2N aqueous hydrochloric acid solution (6.89 ml) was added. The mixture was evaporated to dryness, dried, diluted with water (50 ml) and purified on OASIS resine (ion exchange resin Oasis, HLB 30 μM, Waters) (150 ml). The salts were eluted with water and the product was eluted with 50% Methanol/water. The solvents were evaporated to dryness. The residue was dried at 50° C. to give 2-amino-5-[1-(1-methyl-4-piperidyl)pyrazol-4-yl]pyridine-3-carboxylic acid (1.600 g). NMR Spectrum: (DMSO-d6) 2.02-2.13 (m, 4H), 2.27-2.38 (m, 2H), 2.35 (s, 3H), 2.97-3.06 (m, 2H), 4.13-4.22 (m, 1H), 7.21 (bs, 2H), 7.80 (s, 1H), 8.18 (s, 1H), 8.19 (d, 1H), 8.39 (d, 1H); Mass spectrum: M+H+ 302

1. customThe mixture was evaporated to dryness
2. customdried
3. additiondiluted with water (50 ml)
4. custompurified on OASIS resine (ion exchange resin Oasis, HLB 30 μM, Waters) (150 ml)
5. washThe salts were eluted with water
6. washthe product was eluted with 50% Methanol/water
7. customThe solvents were evaporated to dryness
8. customThe residue was dried at 50° C.