Реакция #319401

Уравнение реакции

(4S)-4-phenylacetamido-3-isoxazolidinone

Compound ( 70 )

1-(4-nitrobenzyl) 3-(2-acetamidoethylthio)-2-oxoglutarate

1-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline

→

subject Compound ( 71 )

Выход 57.3%

4-nitrobenzyl 2-[(4S)-4-phenylacetamido-3-oxo-2-isoxazolidinyl]-3-(2acetamidoethylthio)-5-oxo-2-tetrahydrofurancarboxylate

Выход 57.3%

Растворители

dichloromethane

Условия реакции

Обработка

1. 1
   ДругоеThe solvent was evaporated off
2. 2
   Промывкаfollowed by elution with ethyl acetate

Методика

In 5 ml of dichloromethane were suspended 48 mg of (4S)-4-phenylacetamido-3-isoxazolidinone and 95 mg of the Compound (70) obtained in Example 70. To the suspension was added 71 mg of 1-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline. The mixture was stirred for 5.5 hours at room temperature. The solvent was evaporated off, and the residue was subjected to a silica gel column chromatography, followed by elution with ethyl acetate to give 75 mg of the subject Compound (71) as a colorless oily product.

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