Réaction #72846
ord-c64fce19c9ae4dd1ae929f7848b99444
Équation de réaction
2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid
tromethamine
tromethamine
→
2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid 2-amino-2-(hydroxymethyl)-1,3-propanediol salt
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Température
6°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températurecooled (1 C/min) to 20 C
- 2workup.STIRRINGstirred at 20 C for 8 hours
- 3AutreThe solids were isolated by vacuum filtration
- 4Autredried at 60 C under vacuum for 5 hours
Mode opératoire
To the 2-methyl-1-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid (353.0 mg), methanol (14.0 mL) was added. The slurry was heated to 6° C. and tromethamine (3.0 M solution in water, 1.0 equivalent) was added in four aliquots over 15 minutes followed by the addition of crystalline seeds of crystalline tromethamine salt from batch 1. The slurry was stirred at 60 C for 3 hours, cooled (1 C/min) to 20 C, and stirred at 20 C for 8 hours. The solids were isolated by vacuum filtration, dried at 60 C under vacuum for 5 hours. The yield of the tromethamine salt was 401.5 mg (˜88.9% yield).