Synthesis and Characterization of Impurities of a Common and Advanced Intermediate of Candesartan and Azilsartan Antihypertensive Drugs

References (13)

1. 1 Angiotensin Receptors and Their Antagonists [DOI]
2. 2 Nonpeptide angiotensin II receptor antagonists. Synthesis and biological activity of benzimidazolecarboxylic acids [DOI]
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4. 4 Nonpeptide angiotensin II receptor antagonists. Synthesis and biological activity of benzimidazoles [DOI]
5. 5 One-Pot Synthesis of 1H-Benzimidazole Derivatives Using Thiamine Hydrochloride as a Reusable Organocatalyst [DOI]
6. 6 LC and LC–MS/TOF studies on stress degradation behaviour of candesartan cilexetil [DOI]
7. 7 Hydrolysis and transesterification reactions of candesartan cilexetil observed during the solid phase extraction procedure [DOI]
8. 8 Improved Process for Azilsartan Medoxomil: A New Angiotensin Receptor Blocker [DOI]
9. 9 A novel and practical synthesis of substituted 2-ethoxy benzimidazole: candesartan cilexetil [DOI]
10. 10 Pharmacological profile of a highly potent and long-acting angiotensin II receptor antagonist, 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4- yl]methyl]-1H-benzimidazole-7-carboxylic acid (CV-11974), and its prodrug, (+/-)-1-(cyclohexyloxycarbonyloxy)-ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5- yl)biphenyl-4-yl]methyl]-1H-benzimidazole-7-carboxylate (TCV-116). [DOI]
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12. 12 Synthesis of Azilsartan and Its Selected Potential Impurities [DOI]
13. 13 Identification, synthesis and structural determination of some impurities of candesartan cilexetil [DOI]

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