反应详情

A mixture of 7.6 parts of N-(dihydro-3,3-diphenyl-2(3H)-furanylidene)-N-methylmethanaminium bromide, 4.7 parts of cis-N-(3-methoxy-4-piperidinyl)benzamide, 3.8 parts of sodium carbonate, 0.1 parts of potassium iodide and 240 parts of 4-methyl-2-pentanone was stirred and refluxed for 18 hours using a water-separator. The reaction mixture was cooled to room temperature and washed with water. The organic phase was separated, dried, filtered and evaporated. The oily residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2-oxybispropane. The product was filtered off and dried, yielding 3.5 parts (35% of cis-4-(benzoylamino)-3-methoxy-N,N-dimethyl-α, α-diphenyl-1-piperidinebutanamide; mp. 146.6° C. (compound 122).

1. temperaturerefluxed for 18 hours
2. washwashed with water
3. customThe organic phase was separated
4. customdried
5. filtrationfiltered
6. customevaporated
7. customThe oily residue was purified by column-chromatography over silica gel using
8. additiona mixture of trichloromethane and methanol (95:5 by volume) as eluent
9. customThe pure fractions were collected
10. customthe eluent was evaporated
11. customThe residue was crystallized from 2,2-oxybispropane
12. filtrationThe product was filtered off
13. customdried