An optimized approach in the synthesis of imatinib intermediates and analogues12. Issue 66 (27th June 2016)

• Record Type: Journal Article
• Authors: Kinigopoulou, M.; Filippidou, M.; Gogou, M.; Giannousi, A.; Fouka, P.; Ntemou, N.; Alivertis, D.; Georgis, C.; Brentas, A.; Polychronidou, V.; Voulgari, P.; Theodorou, V.; Skobridis, K.
• Is Part Of: RSC advances. Volume 6:Issue 66(2016)
• Page Start: 61458
• Page End: 61467
• Publication Date: 2016-06-27
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra09812f
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : We revisited the classical synthetic procedure for imatinib synthesis providing an improved and optimized approach in the preparation of a series of new imatinib analogues. Abstract : We revisited the classical synthetic procedure for imatinib synthesis providing an improved and optimized approach in the preparation of a series of new imatinib analogues. The proposed methodology effectively overcomes certain problematic steps, saves time and labor, provides a very high yield and purity and has the potential to be used for the synthesis of many analogues. The formation of the desired guanidine salt4, one of the key steps to the imatinib synthesis, was proceeded almost quantitatively by the reaction of the hydrochloride of the suitable aniline3 with excess of molten cyanamide, without any solvent. Pure arylamine intermediates6a–d were obtained quantitatively in a short reaction time after reduction of the nitro group of the intermediate pyrimidines5a–d with hydrogen over the Adam's catalyst. In addition, the application of this optimized approach can be extended in the synthesis of nilotinib and its analogues intermediates.