Methyl Methanesulfonate → N-methyl-N-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)trifluoroacetamide

Under nitrogen, 0.21 g (5.25 mM) of 60% sodium hydride-liquid paraffin was added to a solution of 1.51 g (4.87 mM) of N-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)trifluoroacetamide in N,N-dimethylformamide (10 ml) at 0° C. and the mixture was stirred at the prevailing temperature for 40 minutes. To this reaction mixture was added 0.5 ml (5.90 mM) of methyl methanesulfonate and the mixture was stirred at room temperature for 112 hours. The mixture was further stirred at 100° C. for 2.5 hours, at the end of which time the reaction was stopped by adding saturated aqueous solution of sodium hydrogen carbonate. The reaction mixture was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride and dried over MgSO4. The crude product thus obtained was purified by column chromatography (ethyl acetate-hexane 40%) to provide the title compound.

1. stirringthe mixture was stirred at room temperature for 112 hours
2. stirringThe mixture was further stirred at 100° C. for 2.5 hours, at the end of which time the reaction
3. extractionThe reaction mixture was then extracted with ethyl acetate
4. washThe organic layer was washed with saturated aqueous solution of sodium chloride
5. dry with materialdried over MgSO4
6. customThe crude product thus obtained
7. customwas purified by column chromatography (ethyl acetate-hexane 40%)

ORD 기록

ord-26f4ce169ab544a38ec3175e834da75e

출처 데이터셋

uspto-grants-2001_05

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06235731B1