Réaction #49052
ord-e1a179c48aa24e148150009a12a9ba8b
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1AutreThen, the reaction vessel was equipped with a reflux condenser
- 2Températurethe mixture was heated at 60° C. for 2 days
- 3AutreAfter completion of the reaction
- 4Extractionthe reaction mixture was extracted with ethyl acetate
- 5Lavagethe organic layer was washed sequentially with water and saturated brine
- 6Séchagedried over anhydrous sodium sulfate
- 7Concentrationconcentrated under reduced pressure
- 8AutreThe resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 4% methanol/methylene chloride as an eluent)
Mode opératoire
Methyl 5-amino-pentanoate hydrochloride {see J. Org. Chem. (1968) 1581} (128 mg, 0.178 mmol) and sodium cyanoborohydride (45 mg, 0.718 mmol) were added to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (115 mg, 0.239 mmol) obtained in Step F of Example 1 in tetrahydrofuran (anhydrous, 4.0 mL). The mixture was stirred at room temperature for 1.5 hours. Then, the reaction vessel was equipped with a reflux condenser, and the mixture was heated at 60° C. for 2 days. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 4% methanol/methylene chloride as an eluent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin-1-ylmethyl)-benzamide (Compound H-4, 42.7 mg, 37%) as a white solid.