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Darifenacin, (S)-2-[1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]-3-pyrrolidinyl]-2,2-diphenyl ace tamide, is an M3-selective receptor antagonist that has been reported to be clinically effective for the treatment of overactive bladder. Darifenacin is generally synthesized by the key reaction of 3-(S)-(+)-(1-cyano-1,1-diphenylmethyl)-pyrrolidine (Imp-2) with 5-halo ethyl-2,3-dihydrobenzofuran (Imp-8) in presence of an organic base to afford 3-(S)-(cyano diphenylmethyl)-1-[2-(2,3-dihydrobenzofuran-5-yl)ethyl]pyrrolidine (Imp-12).