تفاعل #709615

معادلة التفاعل

4-nitrobenzyl (1R,5R,6S)-6-[(1R)-1-hydroxyethyl]-1-methyl-2-oxo-1-carbapenam-3-carboxylate

diisopropylethylamine

2-(3-oxopiperazin-1-yl)-2-iminoethylmercaptan hydrochloride

diisopropylethylamine

diphenylphosphoryl chloride

→

title product

المردود 11.0%

(1R,5S,6S)-2-[2-(3-Oxopiperazin-1-yl)-2-iminoethylthio]-6-[(1R)-1-hydroxyethyl]-1-methyl-1-carbapen-2-em-3-carboxylic acid

المردود 11.0%

المذيبات

tetrahydrofuran

phosphate

acetonitrile

dimethylsulfoxide

ether

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةcooling
2. 2
   workup.ADDITIONwere added to the reaction mixture
3. 3
   workup.STIRRINGthe whole mixture was stirred for 30 minutes with ice-
4. 4
   درجة الحرارةcooling
5. 5
   أخرىthe solvent was decanted off from the gummy material which
6. 6
   أخرىformed
7. 7
   ترشيحThe hydrogenated mixture was filtered over "Celite" (Trade Mark)
8. 8
   ترشيحfilter aid
9. 9
   استخلاصthe filtrate was extracted with 80 ml of ether
10. 10
    تركيزThe aqueous layer was concentrated under reduced pressure

الإجراء التجريبي

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.

المصدر