Methyl iodide → 1,2-Dimethylindole-3-carboxylic acid

Temperatur

-78 °C

Diisopropylamine (2.83 ml, 20.0 mmol) was dissolved in THF (35 ml). Under stirring at −78° C., n-butyl lithium (12.7 ml, 20.0 mmol, a 1.57M hexane solution) was added to the resulting solution. After stirring at 0° C. for 15 minutes, the reaction mixture was cooled again to −78° C. Under stirring, a solution of 1-methyl-1H-indole-3-carboxylic acid (1.75 g, 10.0 mmol) in THF (5 ml) was added. After the reaction mixture was stirred at the same temperature for 30 minutes, methyl iodide (3.42 ml, 55.0 mmol) was added. The reaction mixture was caused to rise back to room temperature over 30 minutes. The reaction mixture was poured into water and the mixture was stirred for 18 hours at room temperature. The reaction mixture was washed with ether. The water layer was acidified with 1M HCl, followed by extraction with ether. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by silica gel chromatography (middle pressure, linear gradient of chloroform/methanol from 10:0 to 20:1, 20 ml/min, φ 50×300 mm) to give 1,2-dimethyl-1H-indole-3-carboxylic acid (180 mg, 10%) as a colorless solid.

1. stirringAfter stirring at 0° C. for 15 minutes
2. temperaturethe reaction mixture was cooled again to −78° C
3. stirringUnder stirring
4. stirringAfter the reaction mixture was stirred at the same temperature for 30 minutes
5. stirringthe mixture was stirred for 18 hours at room temperature
6. washThe reaction mixture was washed with ether
7. extractionfollowed by extraction with ether
8. washThe extract was washed with saturated brine
9. dry with materialdried over anhydrous sodium sulfate
10. distillationdistilled under reduced pressure
11. customto remove the solvent
12. customThe residue was purified by silica gel chromatography (middle pressure, linear gradient of chloroform/methanol from 10:0 to 20:1, 20 ml/min, φ 50×300 mm)

ORD-Eintrag

ord-4f8cd2c46bde453a90ac695006c7cd31

Quelldatensatz

uspto-grants-2007_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07157487B2