反応 #709615
ord-475e6069807b4001ab71732ad3672a6c
反応方程式
反応物
反応条件
後処理
- 1温度cooling
- 2workup.ADDITIONwere added to the reaction mixture
- 3workup.STIRRINGthe whole mixture was stirred for 30 minutes with ice-
- 4温度cooling
- 5その他the solvent was decanted off from the gummy material which
- 6その他formed
- 7ろ過The hydrogenated mixture was filtered over "Celite" (Trade Mark)
- 8ろ過filter aid
- 9抽出the filtrate was extracted with 80 ml of ether
- 10濃縮The aqueous layer was concentrated under reduced pressure
実験手順
0.28 ml of diisopropylethylamine and 0.29 ml of diphenylphosphoryl chloride were added dropwise to an ice-cooled solution of 500 mg of 4-nitrobenzyl (1R,5R,6S)-6-[(1R)-1-hydroxyethyl]-1-methyl-2-oxo-1-carbapenam-3-carboxylate in 6 ml of anhydrous acetonitrile, after which the mixture was stirred for one hour with ice-cooling. 0.20 ml of diisopropylethylamine and a suspension of 452 mg of 2-(3-oxopiperazin-1-yl)-2-iminoethylmercaptan hydrochloride in 3.6 ml of dimethylsulfoxide were added to the reaction mixture, and the whole mixture was stirred for 30 minutes with ice-cooling. The reaction mixture was poured into 200 ml of anhydrous ether and the solvent was decanted off from the gummy material which formed. This material was dissolved in a mixture of 40 ml of tetrahydrofuran and 46 ml of 0.1M phosphate buffer (pH 7.0), and the solution was subjected to hydrogenation for 2 hours at room temperature in the presence of 662 mg of 10% palladium-carbon. The hydrogenated mixture was filtered over "Celite" (Trade Mark) filter aid, and the filtrate was extracted with 80 ml of ether. The aqueous layer was concentrated under reduced pressure, and the concentrate was subjected to chromatography through a 160 ml column of "Dowex 50W" (Trade Mark) cation exchange resin (Na+ type), giving 58 mg of the title product from the fraction eluted with water.