Reaction #1449

Reaction equation

sodium hydride

water

6-(4-nitrobenzoyl)-2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine

methyl iodide

→

6-(4-nitrobenzoyl)-2,3-dimethyl-3,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine

Solvents

N,N-dimethylformamide

chloroform

N,N-dimethylformamide

Conditions

Workup

1. 1
   Temperaturewith cooling on an ice bath
2. 2
   workup.ADDITIONwas then added dropwise a solution
3. 3
   Otherprepared
4. 4
   workup.STIRRINGstirred for 24 hours at room temperature
5. 5
   Otherthe resulting organic layer was separated
6. 6
   Washwashed with a saturated sodium chloride aqueous solution
7. 7
   Dryingdried over anhydrous magnesium sulfate
8. 8
   OtherAfter removing the solvent
9. 9
   workup.DISTILLATIONby distillation under a reduced pressure

Procedure

In a stream of argon, 144 mg of 60% sodium hydride was suspended in a small volume of N,N-dimethylformamide to which, with cooling on an ice bath, was then added dropwise a solution prepared by dissolving 500 mg of 6-(4-nitrobenzoyl)-2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine in 20 ml of N,N-dimethylformamide. After 1 hour of stirring at room temperature, the reaction solution was mixed with 0.11 ml of methyl iodide and stirred for 24 hours at room temperature. The reaction solution was mixed with water and chloroform, and the resulting organic layer was separated, washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After removing the solvent by distillation under a reduced pressure, the thus obtained residue was subjected to silica gel column chromatography to obtain 351 mg of 6-(4-nitrobenzoyl)-2,3-dimethyl-3,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepine from the chloroform-methyl alcohol (30:1) eluate.

Source