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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217309생성일: 2026년 10월 25일

P-Cresol → Tolterodine

https://huagongshe.com/reaction/217309

반응식

참여 물질

역할이름HCID투입량
반응물P-CresolHCID 2879—
반응물2-(3-(Di(propan-2-yl)amino)-1-phenylpropyl)-4-methylphenolHCID 5512—
반응물Methanesulfonic AcidHCID 6395—
반응물N,N-diisopropyl-3-phenylprop-2-en-1-amineHCID 67084639—
생성물TolterodineHCID 44387985%

반응 조건

온도130 °C

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193391B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-144a71ec5a4c4639ba85d8a41b334eed
출처 메모uspto-grants-2012_06