Réaction #709594

Équation de réaction

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

diisopropylethylamine

2-[(3R)-3-carbamoyloxypyrrolidin-1-yl]-2-iminoethylmercaptan hydrochloride

diisopropylethylamine

diphenylphosphoryl chloride

→

title product

Rendement 17.6%

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

Rendement 17.6%

Solvants

tetrahydrofuran

phosphate

acetonitrile

dimethylsulfoxide

ether

Conditions de réaction

Traitement

1. 1
   Températurecooling
2. 2
   workup.STIRRINGthe resulting mixture was stirred for a further 30 minutes with ice-
3. 3
   Températurecooling
4. 4
   Autrethe solvent was decanted off from the gummy material which
5. 5
   Autreformed
6. 6
   FiltrationThe hydrogenated solution was filtered over "Celite" (Trade Mark)
7. 7
   Filtrationfilter aid
8. 8
   Extractionthe filtrate was extracted with 80 ml of ether
9. 9
   ConcentrationThe aqueous layer was concentrated under reduced pressure

Mode opératoire

0.183 ml of diisopropylethylamine and 0.218 ml of diphenylphosphoryl chloride were added dropwise to an ice-cooled solution of 348 mg of p-nitrobenzyl (5R,6S)-6-[(1R)-1-hydroxyethyl]-2-oxo-1-carbapenam-3-carboxylate in 5 ml of anhydrous acetonitrile, and the mixture was stirred for 60 minutes with ice-cooling. A solution of 0.183 ml of diisopropylethylamine and 380 mg of 2-[(3R)-3-carbamoyloxypyrrolidin-1-yl]-2-iminoethylmercaptan hydrochloride in 2.5 ml of dimethylsulfoxide was then added dropwise, and the resulting mixture was stirred for a further 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 35 ml of tetrahydrofuran and 35 ml of 0.1M phosphate buffer (pH 7.0), and the solution was subjected to catalytic hydrogenation for 3 hours at room temperature in the presence of 0.55 g of 10% palladium-carbon. The hydrogenated solution 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 of column of "Dowex 50W" (Trade Mark) cation exchange resin (Na+ type), giving 70 mg of the title product from the fraction eluted with water.

Source