Reaktion #1982176

Reaktionsgleichung

3-(methoxy-methyl-carbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

tert-Butyllithium

5-bromo-1-triisopropylsilanyl-1H-indole

→

3-(1-triisopropylsilanyl-1H-indole-5-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

Ausbeute 56.2%

Lösungsmittel

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe resulting mixture was stirred at −78° C. for 30 minutes
2. 2
   Temperaturto warm to room temperature over a period of 1 hour
3. 3
   SonstigeThe reaction was quenched by addition of a saturated aqueous solution of NH4Cl
4. 4
   Sonstigewas partitioned between water and EtOAc
5. 5
   TrocknenThe organic layer was dried over MgSO4
6. 6
   Filtrationfiltered
7. 7
   Sonstigeevaporated under reduced pressure
8. 8
   SonstigeThe crude residue was purified by flash chromatography (10% to 25% of EtOAc in hexane)

Vorschrift

tert-Butyllithium (1.7 M in pentane, 13 mL, 22.13 mmol) was added to a solution of 5-bromo-1-triisopropylsilanyl-1H-indole (3.54 g, 10.06 mmol) in THF (35 mL) at −78° C. under nitrogen atmosphere. The pale yellow reaction mixture was stirred at −78° C. for 15 minutes, then a solution of 3-(methoxy-methyl-carbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (2.60 g, 10.06 mmol) in THF (5 mL) was slowly added. The resulting mixture was stirred at −78° C. for 30 minutes, then allowed to warm to room temperature over a period of 1 hour. The reaction was quenched by addition of a saturated aqueous solution of NH4Cl and was partitioned between water and EtOAc. The organic layer was dried over MgSO4, filtered and evaporated under reduced pressure. The crude residue was purified by flash chromatography (10% to 25% of EtOAc in hexane) to give 2.66 g (56% yield) of 3-(1-triisopropylsilanyl-1H-indole-5-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester as colorless oil.

Quelle