関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Diisopropylamine | HCID 7912 | — |
| 反応物 | 6-Methyl-4-phenyl-2-chromanol | HCID 11230196 | — |
| 反応物 | 2H-Chromen-2-ol | HCID 13613709 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Palladium hydroxide | HCID 9942167 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Tolterodine hydrochloride | HCID 46911937 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08067594B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-c8d3d19b4c2749f48064780a06ee9f86 |
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| 出典メモ | uspto-grants-2011_11 |
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