Réaction #674303
ord-af896080e51a4cd89c4cdaee491ea0dd
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1AutreThe solution was sonicated at room temperature for 90 min (
- 2Autrethe temperature of sonication bath
- 3Concentrationconcentrated by rotavapor
- 4Autreto give the residue which
- 5AutreThe layers were separated
- 6ExtractionThe aqueous phase was extracted with DCM (3×30 mL)
- 7LavageThe combined organic phase was washed with brine (30 mL)
- 8Séchagedried over anhydrous Na2SO4
- 9Concentrationconcentrated
- 10Autreto give pale yellow solid which
- 11Autrewas purified by CombiFlash [12 g silica gel column; (MeOH/NH4OH=10/1)/DCM: 0-20%]
Mode opératoire
(R)-tert-butyl 2-(4-(6-amino-5-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)pyridin-3-yl)-1H-pyrazol-1-yl)-7-azaspiro[3.5]nonane-7-carboxylate (105 mg, 0.178 mmol, 1.0 equiv) was dissolved in formic acid (6 mL). The solution was sonicated at room temperature for 90 min (the temperature of sonication bath reached about 40° C. after 90 min). The solution was cooled to room temperature and concentrated by rotavapor to give the residue which was dissolved in EtOAc (20 mL). A solution of Na2CO3 (2.0 M, 20 mL) was added. The mixture was stirred at room temperature for 30 min. H2O (10 mL) was added. The layers were separated. The aqueous phase was extracted with DCM (3×30 mL). The combined organic phase was washed with brine (30 mL), dried over anhydrous Na2SO4, concentrated to give pale yellow solid which was purified by CombiFlash [12 g silica gel column; (MeOH/NH4OH=10/1)/DCM: 0-20%] to afford 77 mg (yield 88%) of (R)-5-(1-(7-azaspiro[3.5]nonan-2-yl)-1H-pyrazol-4-yl)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)pyridin-2-amine as a off-white foam solid.