Реакция #1987364

Уравнение реакции

2-(4-cyanophenoxy)-1-methylethylamine

N-methylpiperidine

(2S)-2-tert-butoxycarbonylaminobutyric acid

isobutyl chloroformate

→

desired product

Выход 56.2%

2-tert-butoxycarbonylamino-N-[2-(4-cyanophenoxy)-1-methylethyl]-(2S)-butyramide

Выход 56.2%

Растворители

Water

methylene chloride

Условия реакции

Обработка

1. 1
   workup.ADDITIONwas added to the mixture at -20° C.
2. 2
   Температураwarm naturally to room temperature
3. 3
   workup.STIRRINGwhile being stirred
4. 4
   workup.STIRRINGwas stirred for 20 hours at room temperature
5. 5
   ПромывкаAfter the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water
6. 6
   Сушкаthe organic layer was dried over anhydrous magnesium sulfate
7. 7
   Другоеthe methylene chloride was removed under reduced pressure
8. 8
   ДругоеThe residue was purified by column chromatography on silica gel

Методика

0.5 g of N-methylpiperidine was added to a solution containing 1.0 g of (2S)-2-tert-butoxycarbonylaminobutyric acid dissolved in 40 ml of methylene chloride, at -20° C. After the mixture was stirred for 10 minutes at the same temperature, 0.7 g of isobutyl chloroformate was added to the mixture at -20° C., and stirred for 1 hour at -20° C. 0.9 g of 2-(4-cyanophenoxy)-1-methylethylamine was added to this mixture at -60° C., and then the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 20 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus obtaining 1.0 g of the desired product in the form of a glutinous substance (yield: 54%).

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