Triethylamine → (S)-1-(2-azido-propyl)-7-methyl-1,4-dihydro-indeno[1,2-b]pyrrole

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Reaction Steps

1.8 ml of methanesulfonyl chloride were added dropwise while stirring to a solution, cooled to 0°, of 2.7 g of (R)-1-(7-methyl-1,4-dihydro-indeno[1,2-b]pyrrol-1-yl)-propan-2-ol and 6.7 ml of triethyl-amine in 75 ml of dichloromethane and the mixture was stirred at this temperature for an additional 1.5 hours. The reaction mixture was subsequently diluted with 200 ml of dichloromethane, washed twice with 90 ml of saturated sodium hydrogen carbonate solution each time and the combined aqueous phases were extracted once with 90 ml of dichloromethane. The combined organic phases were washed with 100 ml of saturated sodium chloride solution, dried over magnesium sulfate and evaporated in a vacuum. The brown oil obtained was dissolved in 70 ml of anhydrous dimethylformamide, treated with 1.55 g of sodium azide and the reaction mixture was heated to 60° for 15 hours while stirring. After cooling, the solution was poured into 150 ml of water and extracted twice with 150 ml of ethyl acetate each time. The combined organic phases were washed once with 120 ml of water and once with 120 ml of saturated sodium chloride solution, dried over magnesium sulfate and the solution was concentrated in a vacuum. The brown oil obtained was purified by column chromatography on silica gel (toluene). 1.5 g (50%) of (S)-1-(2-azido-propyl)-7-methyl-1,4-dihydro-indeno[1,2-b]pyrrole were obtained as a light yellow oil.

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