تفاعل #2481505

معادلة التفاعل

isobutyl chloroformate

N-methylpiperidine

2-(4-cyanophenoxy)-1-methylethylamine

N-(4-methylbenzyloxycarbonyl)-L-valine

→

desired product

المردود 26.8%

N1 -[2-(4-cyanophenoxy)-1-methylethyl]-N2 -phenoxycarbonyl-L-valinamide

المردود 26.8%

المذيبات

methylene chloride

Water

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONwas added to the mixture
2. 2
   درجة الحرارةwarm naturally to room temperature
3. 3
   workup.STIRRINGwhile being stirred
4. 4
   workup.STIRRINGThe whole mixture was stirred for 20 hours at room temperature
5. 5
   غسيلAfter the methylene chloride layer was washed successively with a 5% aqueous solution of sodium bicarbonate and water
6. 6
   تجفيفthe organic layer was dried over anhydrous magnesium sulfate
7. 7
   أخرىthe methylene chloride was removed under reduced pressure
8. 8
   أخرىwas purified by column chromatography on silica gel

الإجراء التجريبي

0.6 g of N-methylpiperidine was added to a solution containing 1.5 g of N-(4-methylbenzyloxycarbonyl)-L-valine dissolved in 100 ml of methylene chloride, at -20° C. After the mixture was stirred for 10 minutes at the same temperature, 0.8 g of isobutyl chloroformate was added to the mixture, and subsequently the whole mixture was stirred for 1 hour at -20° C. 1.0 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. The whole mixture 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, which was a crude crystal, was purified by column chromatography on silica gel, thus yielding 0.6 g of the desired product in the form of light white powder (yield: 28%).

المصدر