Reaction #65494
ord-0ce4a9a0b859482abf544ddf922c98a5
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1Temperatureat reflux temperature
- 2OtherAfter evaporation
- 3Otherto dry
- 4ExtractionThe product was extracted three times with 120 parts of trichloromethane
- 5OtherThe combined extracts were dried
- 6Filtrationfiltered
- 7Otherevaporated
- 8OtherThe residue was purified by column chromatography over silica gel using
- 9workup.ADDITIONa mixture of trichloromethane and methanol (95:5 by volume) as eluent
- 10OtherThe pure fractions were collected
- 11Otherthe eluent was evaporated
- 12workup.ADDITIONThe residue was convened into the hydrochloride salt in a mixture of 2-propanone and ethanol
- 13FiltrationThe salt was filtered off
- 14Othercrystallized from a mixture of ethanol and 2-propanone
- 15FiltrationThe product was filtered off
- 16Otherdried
Procedure
A mixture of 6.2 parts of 4-[1-(1H-imidazol-1-yl)-2-methylpropyl]-1,2-benzenediamine, 6.5 parts of ethyl ethanimidate hydrochloride and 80 parts of ethanol was stirred for 3 hours at reflux temperature. After evaporation to dry, the residue was taken up in water and sodium carbonate. The product was extracted three times with 120 parts of trichloromethane. The combined extracts were dried, filtered and evaporated. The 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 convened into the hydrochloride salt in a mixture of 2-propanone and ethanol. The salt was filtered off and crystallized from a mixture of ethanol and 2-propanone. The product was filtered off and dried, yielding 4 parts (44% ) of 5-[1-(1H-imidazol-1yl)-2-methylpropyl]-2-methyl-1H-benzimidazole dihydrochloride.monohydrate; mp. 214.8° C. (comp. 22).