تفاعل #42449

ord-a947873d89804a60ae57d2f24f7a0ae0

المذيبات

ظروف التفاعل

درجة الحرارة
70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe mixture was partitioned between water and ethyl acetate
  2. 2
    أخرىthe layers were separated
  3. 3
    غسيلthe organic layer washed three times with water
  4. 4
    تجفيفThe organic layer was dried over anhydrous sodium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated
  7. 7
    workup.DISSOLUTIONThe residue was dissolved in methanol (5 mL) to which
  8. 8
    workup.ADDITIONwas added 1N NaOH (2 mL)
  9. 9
    درجة الحرارةthe mixture heated to 50° C. for 1 h
  10. 10
    درجة الحرارةThe mixture was cooled to room temperature
  11. 11
    workup.ADDITIONpoured into water
  12. 12
    غسيلwashed with ether
  13. 13
    استخلاصthe product extracted into ethyl acetate which
  14. 14
    تجفيفwas dried over anhydrous sodium sulfate
  15. 15
    ترشيحfiltered
  16. 16
    تركيزconcentrated to dryness

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07727997B2uspto-grants-2010_06