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137898-68-1

1-methyl-2-(piperazin-1-yl)-1H-benzo[d]imidazole synthesis

3synthesis methods
-

Yield:137898-68-1 69%

Reaction Conditions:

at 150; for 0.5 h;

Steps:

3.2

Step 2 0.43 g (5.0 mmol) of piperazine and 0.24 g (1.0 mmol) of the compound obtained in Step 1 were placed in a dried round flask provided with nitrogen gas, followed by reacting the mixture at 150°C for 30 mins. After cooling to room temperature, the reaction mixture was acidified with IN-HCl solution and washed with dichloromethane. The water layer was treated with IN-NaOH solution and extracted with dichloromethane. The formed organic layer was dried over anhydrous magnesium sulfate and concentrated under a reduced pressure, and the resulting residue was subjected to silica gel column chromatography (dichloromethaneimethanol^il) to obtain 0.15 g of l-methyl-2-(piperazin-l-yl)-benzoimidazole (yield: 69%).

References:

WO2008/153325,2008,A1 Location in patent:Page/Page column 27