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HRID 217309作成日:2026年10月26日

P-Cresol → Tolterodine

https://huagongshe.com/reaction/217309

反応式

関与物質

役割名称HCID仕込み量
反応物P-CresolHCID 2879—
反応物2-(3-(Di(propan-2-yl)amino)-1-phenylpropyl)-4-methylphenolHCID 5512—
反応物Methanesulfonic AcidHCID 6395—
反応物N,N-diisopropyl-3-phenylprop-2-en-1-amineHCID 67084639—
生成物TolterodineHCID 44387985%

反応条件

温度130 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193391B2
出典データセットuspto-grants-2012_06
ORD IDord-144a71ec5a4c4639ba85d8a41b334eed
出典メモuspto-grants-2012_06