反应详情

温度

120 °C

To methyl 6-bromo-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylate (1.3 g, 4.19 mmol) and copper(I) iodide (1.0 g, 5.25 mmol) was added NMP (8 mL). To the mixture was added dropwise a solution of sodium methoxide 25 wt % in methanol (4.0 mL, 17.49 mmol) with stirring. The reaction was heated to 120° C. and stirred for 1.5 hr. The reaction was allowed to cool and when the temperature reached 80° C., water (200 uL) was added. The reaction was allowed to continue to cool to RT and stirred overnight. The reaction was acidified with 1N HCl (17 mL) and diluted with water and EtOAc. The mixture was filtered through Celite and washed with EtOAc. The filtrate was poured into a separatory funnel and the organic phase was separated, washed with brine, dried (MgSO4), filtered, and concentrated under vacuum. Purification by silica gel chromatography (Analogix, SF25-60g, 20 to 50% EtOAc in hexanes) gave after concentration, trituration with hexanes, filtration and drying under vacuum 3-methyl-1-(1-methylethyl)-6-(methyloxy)-1H-indole-4-carboxylic acid (825 mg, 3.34 mmol, 80% yield) as an light yellow solid. MS(ES)+ m/e 248.3 [M+H]+.

1. stirringstirred for 1.5 hr
2. temperatureto cool
3. customreached 80° C.
4. temperatureto cool to RT
5. stirringstirred overnight
6. filtrationThe mixture was filtered through Celite
7. washwashed with EtOAc
8. additionThe filtrate was poured into a separatory funnel
9. customthe organic phase was separated
10. washwashed with brine
11. dry with materialdried (MgSO4)
12. filtrationfiltered
13. concentrationconcentrated under vacuum
14. customPurification by silica gel chromatography (Analogix, SF25-60g, 20 to 50% EtOAc in hexanes)
15. customgave
16. concentrationafter concentration, trituration
17. filtrationwith hexanes, filtration