반응 #8195

반응 방정식

Water

2-Chloro-nicotinonitrile

[2-(7-Hydroxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester

sodium hydride

→

{2-[7-(3-cyano-pyridin-2-yloxy)-1H-indol-3-yl]-1,1-dimethyl-ethyl}-carbamic acid tert-butyl ester

수율 96.0%

용매

dimethylformamide

반응 조건

후처리

1. 1
   온도the mixture is heated in an oil bath to eighty degrees Celsius for 15 hours, under nitrogen
2. 2
   기타to quench
3. 3
   기타the reaction
4. 4
   추출the mixture is extracted three times with 50 mL of ethyl acetate
5. 5
   세척washed twice with 50 mL of 1.00 N sodium hydroxide
6. 6
   건조The organic layer is dried with sodium sulfate
7. 7
   여과filtered
8. 8
   기타the solvent evaporated
9. 9
   workup.DISSOLUTIONThe residue is dissolved in dichloromethane
10. 10
    기타purified

실험 절차

To a solution of [2-(7-Hydroxy-1H-indol-3-yl)-1,1-dimethyl-ethyl]-carbamic acid tert-butyl ester (274 mg, 0.900 mmol) in dimethylformamide (15 mL) is added sodium hydride (26 mg, 1.07 mmol). The mixture is stirred at ambient temperature for 25 minutes under nitrogen. 2-Chloro-nicotinonitrile (187 mg, 1.35 mmol) is added and the mixture is heated in an oil bath to eighty degrees Celsius for 15 hours, under nitrogen. Water (50 ml) is added to quench the reaction and the mixture is extracted three times with 50 mL of ethyl acetate. The organic layers are combined and washed twice with 50 mL of 1.00 N sodium hydroxide. The organic layer is dried with sodium sulfate, filtered and the solvent evaporated. The residue is dissolved in dichloromethane and purified using silica gel chromatography (6% 2M ammonia in methanol, 94% dichloromethane used as mobile phase) to give 350 mg (96%) of {2-[7-(3-cyano-pyridin-2-yloxy)-1H-indol-3-yl]-1,1-dimethyl-ethyl}-carbamic acid tert-butyl ester. FDMS m/e=407 (M++1).

출처