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HRID 563873作成日:2026年10月26日

Hydrochloric Acid → Tolterodine hydrochloride

https://huagongshe.com/reaction/563873

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DiisopropylamineHCID 7912—
反応物6-Methyl-4-phenyl-2-chromanolHCID 11230196—
反応物2H-Chromen-2-olHCID 13613709—
反応物HCID 178418361HCID 178418361—
触媒Palladium hydroxideHCID 9942167—
溶媒MethanolHCID 887—
生成物Tolterodine hydrochlorideHCID 46911937—

反応条件

温度55 °C

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067594B2
出典データセットuspto-grants-2011_11
ORD IDord-c8d3d19b4c2749f48064780a06ee9f86
出典メモuspto-grants-2011_11