تفاعل #992762

معادلة التفاعل

N-(4-amino-2,6-diisopropyl-phenyl)-4-methyl-benzenesulfonamide

N,N-diisopropyl-ethylamine

N-methylpyrrolidine

bis-(2-bromoethyl)ether

→

title compound

المردود 99.0%

2,6-Diisopropyl-4-morpholin-4-yl-phenylamine

المردود 99.0%

المذيبات

ethyl acetate

ظروف التفاعل

المعالجة

1. 1
   غسيلwashed with brine (30 mL) and saturated aqueous potassium carbonate (30 mL)
2. 2
   تجفيفdried over sodium sulfate
3. 3
   تركيزThe organic phase was concentrated in vacuo
4. 4
   workup.DISSOLUTIONredissolved in a mixture of sulfuric acid (1.9 mL) and water (0.1 mL)
5. 5
   workup.ADDITIONIce (30 mL) and water (30 mL) were added
6. 6
   استخلاصThe mixture was extracted with ethyl acetate (3×20 mL)
7. 7
   تجفيفthe combined organic phases were dried over sodium sulfate
8. 8
   تركيزconcentrated in vacuo

الإجراء التجريبي

A mixture of N-(4-amino-2,6-diisopropyl-phenyl)-4-methyl-benzenesulfonamide (346 mg), bis-(2-bromoethyl)ether (151 μL), N,N-diisopropyl-ethylamine (0.53 mL) and N-methylpyrrolidine (1.0 mL) was heated to 180° C. for 20 minutes in a sealed microwave process vial. The mixture was diluted with ethyl acetate (20 mL), washed with brine (30 mL) and saturated aqueous potassium carbonate (30 mL) and dried over sodium sulfate. The organic phase was concentrated in vacuo and redissolved in a mixture of sulfuric acid (1.9 mL) and water (0.1 mL) and stirred at 40° C. for 3 hours. Ice (30 mL) and water (30 mL) were added and the mixture was basified with solid potassium carbonate. The mixture was extracted with ethyl acetate (3×20 mL) and the combined organic phases were dried over sodium sulfate and concentrated in vacuo to furnish 260 mg (99%) of the title compound as a white solid. NMR (500 MHz, CDCl3): 1.26 (d, 12H), 2.95 (m, 2H), 3.06 (m, 4H), 3.49 (b, 2H), 3.87 (m, 4H), 6.69 (s, 2H).

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