関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | P-Cresol | HCID 2879 | — |
| 反応物 | 2-(3-(Di(propan-2-yl)amino)-1-phenylpropyl)-4-methylphenol | HCID 5512 | — |
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | N,N-diisopropyl-3-phenylprop-2-en-1-amine | HCID 67084639 | — |
| 生成物 | Tolterodine | HCID 443879 | 85% |
反応手順
10.2 g of N,N-diisopropyl-3-phenylprop-2-en-1-amine, is added 20.5 g p-cresol and 15.8 g methanesulfonic acid and heated to 130° C. for 6 hours. Chromatography shows disappearance of the peak corresponding N,N-diisopropyl-3-phenylprop-2-en-1-amine, and a fine peak at the retention time of 3-(2-hydroxy-5-methylphenyl)-N,N-diisopropyl-3-phenylpropylamine. From the reaction mixture the (+)-(R)-3-(2-hydroxy-5-methylphenyl)-N,N-diisopropyl-3-phenylpropylamine is isolated as follows: Water and toluene (200 ml each) are added to the reaction mixture and pH adjusted to 9.5. The toluene layer is isolated and washed with water. Distilling off the toluene leaves an oily mass. This is taken up in 300 ml 2-propanol, added 0.55 eq tartaric acid and 0.55 eq formic acid, After stirring overnight, the suspension is filtered. The wet filter cake is approximately 97% pure. The wet filter cake is taken up in 300 ml 2-propanol and heated to reflux, cooled to 5° C., filtered and dried (yield 85%). Purity on HPLC (achiral) 99.5%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08193391B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-144a71ec5a4c4639ba85d8a41b334eed |
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| 出典メモ | uspto-grants-2012_06 |
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