Reaction #4112

Reaction equation

9-bromo-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-one

4-methylpiperidine

→

product

Yield 83.0%

9-Bromo-6-(4-methyl-1-piperidinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine

Yield 83.0%

Solvents

toluene

Conditions

Workup

1. 1
   Temperaturewas heated under nitrogen
2. 2
   Otherresulted
3. 3
   TemperatureThe mixture was refluxed for 3 hours
4. 4
   Filtrationfiltered
5. 5
   workup.STIRRINGThe filtrate was stirred with 500 ml of 2N sodium hydroxide solution for 15 minutes
6. 6
   Otherthe layers were separated
7. 7
   ExtractionThe aqueous phase was extracted with 250 ml of toluene
8. 8
   Washwashed once with 2N sodium hydroxide solution, twice with water
9. 9
   Dryingdried over anhydrous sodium sulfate
10. 10
    Filtrationfiltered
11. 11
    Concentrationconcentrated in vacuo to an oil which
12. 12
    OtherThe solid was triturated twice with hexane

Procedure

A mixture of 4.73 g (0.0150 mole) of 9-bromo-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-one and 1000 ml of toluene was heated under nitrogen, with stirring, until a solution resulted. Then there was added 14.9 g (0.150 mole) of 4-methylpiperidine, followed by 8.54 g (0.045 mole) of titanium tetrachloride. The mixture was refluxed for 3 hours, cooled to room temperature and filtered. The filtrate was stirred with 500 ml of 2N sodium hydroxide solution for 15 minutes and the layers were separated. The aqueous phase was extracted with 250 ml of toluene. The toluene layers were combined, washed once with 2N sodium hydroxide solution, twice with water, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to an oil which solidified. The solid was triturated twice with hexane to afford 4.9 g (83%) of product. Recrystallization from ethyl acetate provided the analytical sample, mp 177°-179° C.

Source