تفاعل #42449
ord-a947873d89804a60ae57d2f24f7a0ae0
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىThe mixture was partitioned between water and ethyl acetate
- 2أخرىthe layers were separated
- 3غسيلthe organic layer washed three times with water
- 4تجفيفThe organic layer was dried over anhydrous sodium sulfate
- 5ترشيحfiltered
- 6تركيزconcentrated
- 7workup.DISSOLUTIONThe residue was dissolved in methanol (5 mL) to which
- 8workup.ADDITIONwas added 1N NaOH (2 mL)
- 9درجة الحرارةthe mixture heated to 50° C. for 1 h
- 10درجة الحرارةThe mixture was cooled to room temperature
- 11workup.ADDITIONpoured into water
- 12غسيلwashed with ether
- 13استخلاصthe product extracted into ethyl acetate which
- 14تجفيفwas dried over anhydrous sodium sulfate
- 15ترشيحfiltered
- 16تركيزconcentrated 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.