Butyl iodide → 1-Butyl-4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylic acid

温度

70 °C

To a mixture of methyl 4-[methyl(methylsulfonyl)amino]-1H-indole-6-carboxylate (0.437 g) in DMF (15 mL) was added potassium hydroxide (0.087 g) and iodobutane (0.34 mL). The mixture was heated to 70° C. for 6 h. then stirred at room temperature for 72 h. The mixture was partitioned between water and ethyl acetate, the layers were separated and the organic layer washed three times with water. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was dissolved in methanol (5 mL) to which was added 1N NaOH (2 mL) and the mixture heated to 50° C. for 1 h. The mixture was cooled to room temperature and poured into water and washed with ether. The aqueous layer was acidified to pH 4 with 1N HCl and the product extracted into ethyl acetate which was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to give 0.377 g of the title compound: 1H NMR (CDCl3) δ 0.973, 1.38, 1.87, 3.01, 3.45, 4.21, 6.71, 7.36, 7.82, 8.18.

1. customThe mixture was partitioned between water and ethyl acetate
2. customthe layers were separated
3. washthe organic layer washed three times with water
4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
5. filtrationfiltered
6. concentrationconcentrated
7. dissolutionThe residue was dissolved in methanol (5 mL) to which
8. additionwas added 1N NaOH (2 mL)
9. temperaturethe mixture heated to 50° C. for 1 h
10. temperatureThe mixture was cooled to room temperature
11. additionpoured into water
12. washwashed with ether
13. extractionthe product extracted into ethyl acetate which
14. dry with materialwas dried over anhydrous sodium sulfate
15. filtrationfiltered
16. concentrationconcentrated to dryness

ORDレコード

ord-a947873d89804a60ae57d2f24f7a0ae0

出典データセット

uspto-grants-2010_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07727997B2