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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563873Erstellt: 25. Oktober 2026

Hydrochloric Acid → Tolterodine hydrochloride

https://huagongshe.com/reaction/563873

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiisopropylamineHCID 7912—
Edukt6-Methyl-4-phenyl-2-chromanolHCID 11230196—
Edukt2H-Chromen-2-olHCID 13613709—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladium hydroxideHCID 9942167—
LösungsmittelMethanolHCID 887—
ProduktTolterodine hydrochlorideHCID 46911937—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To the crude solution from Step A was added methanol (125 ml, 5 ml/g cresol) and diisopropylamine (92 ml, 0.693 mol, 3 equiv). The mixture was then hydrogenated over 20 wt % Pd(OH)2/C wet (5.6 g, 10 wt % theory of the benzopyran-2-ol) at 110° C. under 586×103 Nm−2 (85 psi) hydrogen pressure. Reaction progress was monitored by HPLC (completion usually occurs between 16 and 24 h). Upon completion, the mixture was cooled, purged with nitrogen, filtered and washed with toluene (2×25 ml). The filtrate was then azeotroped with toluene to remove all methanol and diisopropylamine to end at a final volume corresponding to 10 ml/g cresol. The solution was then stirred at 50-60° C. and 37% HCl (19.3 ml, 0.231 mol, 1.0 equiv c.f cresol) was added resulting in the precipitation of racemic tolterodine hydrochloride. The suspension was cooled to 25° C. and stirred for 2 h, then filtered and washed with toluene (2×50 ml). Racemic tolterodine hydrochloride was then dried under vacuum at 50° C. Yield was 52.7 g, 63% from p-cresol with achiral purity of 97%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08067594B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-c8d3d19b4c2749f48064780a06ee9f86
Quellennotizuspto-grants-2011_11