反応 #1117307

反応方程式

(2S, 4S)-2-carbamoyl-1,1-dimethyl-4-mercaptopyrrolidinium

diisopropylethylamine

diphenylphosphoryl chloride

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

→

title compound

(5R, 6S)-2-[(2S, 4S)-2-Carbamoyl-1,1-dimethylpyrrolidinium-4-ylthio]-6-[(1R)-1-hydroxyethyl]-1-carbapen-2-em-3-carboxylate

溶媒

acetonitrile

acetonitrile

diethyl ether

反応条件

後処理

1. 1
   温度cooling
2. 2
   workup.ADDITIONwas added to the mixture, whilst ice-
3. 3
   温度cooling
4. 4
   workup.WAITto stand for 4 hours at the same temperature
5. 5
   workup.WAITfor 2 days in a refrigerator
6. 6
   洗浄the resulting deposit was washed repeatedly by decantation
7. 7
   workup.DISSOLUTIONThe crude product was dissolved in a mixture of 30 ml of tetrahydrofuran and 30 ml of a 0.1M phosphate buffer (pH 7.0) and hydrogenated at room temperature for 2.5 hours in the presence of 450 mg of 10% w/w palladium-on-charcoal
8. 8
   その他At the end of this time, insoluble materials were removed by filtration
9. 9
   ろ過filter aid
10. 10
    濃縮The aqueous layer was concentrated by evaporation under reduced pressure
11. 11
    洗浄Fractions eluted with water
12. 12
    その他were collected

実験手順

210 μl of diisopropylethylamine and 250 μl of diphenylphosphoryl chloride were simultaneously added, whilst ice-cooling, to a solution of 400 mg of 4-nitrobenzyl (5R, 6S)-6-[(1R)-1-hydroxyethyl]-2oxo-1-carbapenam-3-carboxylate dissolved in 5 ml of dry acetonitrile, and the mixture was stirred for 1 hour, whilst ice-cooling. At the end of this time, a solution of 447 mg of the crude (2S, 4S)-2-carbamoyl-1,1-dimethyl-4-mercaptopyrrolidinium salt prepared as described in Example 1-(1) in 5 ml of dry acetonitrile was added to the mixture, whilst ice-cooling, and then the mixture was allowed to stand for 4 hours at the same temperature and then for 2 days in a refrigerator. The reaction mixture was then poured into diethyl ether and the resulting deposit was washed repeatedly by decantation. The crude product was dissolved in a mixture of 30 ml of tetrahydrofuran and 30 ml of a 0.1M phosphate buffer (pH 7.0) and hydrogenated at room temperature for 2.5 hours in the presence of 450 mg of 10% w/w palladium-on-charcoal. At the end of this time, insoluble materials were removed by filtration using a Celite filter aid. The aqueous layer was concentrated by evaporation under reduced pressure, and the residue was transferred to a column packed with Diaion HP-20AG (Mitsubishi Chemicals Industries, Ltd.). Fractions eluted with water were collected and lyophilized to afford the title compound as a powder. This was further purified using a Lobar column (Merck, LiChroprep RP-8 size B) and fractions eluted with a 5% by volume aqueous methanolic solution were collected and concentrated by evaporation under reduced pressure followed by lyophilization, to afford 208 mg of the title compound.

出典